The Hydrogen Atom, Part 1 of 3: Intro to Quantum Physics

Richard Behiel
2 Jun 202318:34

Summary

TLDRDieses Video skizziert die Grundlagen der Quantenmechanik anhand des Wasserstoffatoms, das aus einem Protonen und einem Elektron besteht. Es erklärt, wie das Elektron trotz der Anziehungskraft nicht auf das Proton kollabiert und wie die Quantenunschärfe die Bewegung des Elektrons beeinflusst. Der Fokus liegt auf der Darstellung der Wellenfunktion, der Wahrscheinlichkeitsdichte und dem sogenannten reduzierten Planckschen Wirkung, die die Beziehung zwischen Energie, Frequenz und Impuls definiert. Darüber hinaus wird die Schrödinger-Gleichung vorgestellt, die die Bewegung des Elektrons beschreibt, und es wird die Lösung dieser Gleichung in sphärischen Koordinaten diskutiert.

Takeaways

  • 🌌 Der Wasserstoffatom ist ein Portal zwischen der Welt der Experimente und der seltsamen Welt der Quantenmechanik.
  • 🔬 Der Elektron und das Proton im Wasserstoffatom interagieren durch die Coulomb-Wechselwirkung, die das Elektron in Richtung des Protons zieht.
  • 🚀 Die Quantenmechanik verhindert, dass das Elektron in das Proton zusammenfällt, da die Unsicherheit der Position und der Impuls die Kollapsenergie verhindert.
  • 🤔 Die Elektronenbahnen im Wasserstoffatom können durch Absorption von Photonen in höhere Energiezustände übergehen, was jedoch metastabil ist und schnell zurück in den Grundzustand übergeht.
  • 🔄 Die Quantenmechanik erfordert, dass man die genaue Position eines Teilchens nicht bestimmen kann, ohne seine Impulsinformation zu verlieren.
  • 🌐 Die sogenannte 'Quantenverschmierung' ist ein fundamentales Merkmal der Quantenmechanik, das die Lokalisierung eines Teilchens verhindert.
  • 📏 Die Masse des Protons ist 1836-mal größer als die des Elektrons, was bedeutet, dass das Proton weniger 'verschmiert' ist und als fixer Punkt im Koordinatensystem betrachtet werden kann.
  • 📚 Die Wellenfunktion (PSI) ist eine komplexe Funktion von Raum und Zeit und bildet die Grundlage für die Beschreibung des Zustands eines Quantensystems.
  • 🧩 Die Hamilton-Operatoren in der Quantenmechanik beschreiben die Energie des Systems und ermöglichen die Lösung des Schrödinger-Gleichungen für Energieeigenzustände.
  • 🔗 Die Lösung des Schrödinger-Gleichungs für das Wasserstoffatom liefert die Energieeigenwerte und die zugehörigen Wellenfunktionen, die die möglichen Zustandsbeschreibungen des Elektrons darstellen.

Q & A

  • Was ist der Grund, warum der Elektron nicht in den Proton fällt?

    -Der Grund, warum das Elektron nicht in den Proton fällt, liegt in der Quantenmechanik. Die Unsicherheitsrelation zwischen Ort und Impuls verhindert, dass das Elektron exakt lokalisiert werden kann, was eine Kollapse des Elektrons verhindert.

  • Was ist die Bedeutung von 'Quantenfuzziness' im Kontext des Wasserstoffatoms?

    -Quantenfuzziness bezieht sich auf die Unsicherheit der Position eines Quantenteilchens, wie das Elektron im Wasserstoffatom. Diese Unsicherheit verhindert, dass das Elektron in den Proton kollabiert.

  • Wie wird die Energie des Elektrons im Wasserstoffatom quantisiert?

    -Die Energie des Elektrons im Wasserstoffatom wird durch die Lösung des zeitunabhängigen Schrödinger-Gleichungen quantisiert, was zu diskreten Energieniveaus führt, die als Energieeigenwerte bezeichnet werden.

  • Was ist die Rolle des Planckschen Wirkungsquantums (h-bar) in der Quantenmechanik?

    -Das Plancksche Wirkungsquantum (h-bar) ist eine fundamentale Konstante in der Quantenmechanik, die die Beziehung zwischen Energie und Frequenz sowie zwischen Impuls und Ort definiert.

  • Wie wird die Bewegung des Elektrons im Wasserstoffatom mathematisch beschrieben?

    -Die Bewegung des Elektrons im Wasserstoffatom wird durch die WellenfunktionPsi beschrieben, die eine komplexe Funktion von Ort und Zeit ist.

  • Was ist der Hamilton-Operator und welche Rolle spielt er in der Schrödinger-Gleichung?

    -Der Hamilton-Operator ist eine Differentialoperator, die die Energie eines Systems in Abhängigkeit von Ort und Impuls darstellt. Er ist zentral in der Schrödinger-Gleichung, die die zeitabhängige Entwicklung der Wellenfunktion beschreibt.

  • Wie wird die kinetische Energie im Rahmen der Quantenmechanik dargestellt?

    -In der Quantenmechanik wird die kinetische Energie durch den Betrag des Impulsoperators, das heißt durch die quadrierte Gradientenableitung der Wellenfunktion, dargestellt.

  • Was ist die Bedeutung des magnetischen Quantenzahlen im Zusammenhang mit dem Wasserstoffatom?

    -Die magnetische Quantenzahl ist ein Index, der die Richtung des Orbitals im Raum beschreibt. Sie ist ein wichtiger Parameter in der Lösung des Schrödinger-Gleichungs für das Wasserstoffatom.

  • Wie wird die Potentialenergie des Elektrons im Wasserstoffatom berechnet?

    -Die Potentialenergie des Elektrons im Wasserstoffatom wird durch die klassische Coulomb-Potentialformel berechnet, die die elektrostatische Wechselwirkung zwischen dem Elektron und dem Proton beschreibt.

  • Was sind 'Energieeigenzustände' und wie sind sie mit der Lösung des Schrödinger-Gleichungs verbunden?

    -Energieeigenzustände sind spezielle Lösungen der Wellenfunktion, die sich nicht im Raum, sondern nur in der komplexen Ebene verändern. Sie sind mit diskreten Energieniveaus verbunden, die durch die Lösung des zeitunabhängigen Schrödinger-Gleichungs gefunden werden.

  • Wie wird die sphärische Symmetrie des Wasserstoffatoms in der Lösung des Schrödinger-Gleichungs ausgenutzt?

    -Die sphärische Symmetrie des Wasserstoffatoms wird durch die Verwendung von sphärischen Koordinaten (R, Theta, Phi) ausgenutzt, was die Lösung des Schrödinger-Gleichungs erleichtern kann.

Outlines

00:00

🌌 Grundzustand des Wasserstoffatoms

In diesem Absatz wird das Wasserstoffatom im Grundzustand beschrieben, bestehend aus einem Protonen und einem Elektron. Der Elektron ist so nah am Protonen wie möglich, bis die Quantenunsicherheit einsetzt. Es wird eine Photon verschossen, um die Reaktion zu beobachten. Das Elektron wird in einen höheren Energiezustand versetzt, der jedoch metastabil ist und bald zurück in den Grundzustand übergeht, wobei das ursprüngliche Photon zurückgeworfen wird. Dies zeigt die Erhaltung der Energie. Es wird auch ein weiteres Photon verschossen, das einen Zustand mit Rotationsmoment aufweist. Der Absatz endet mit einer Meditation über die Situation, die die Verbindung zwischen der Welt der Experimente und der seltsamen Welt der Quantenmechanik hervorhebt.

05:01

🔬 Quantenmechanik und das Wasserstoffatom

Dieser Absatz behandelt die Frage, warum das Elektron nicht in das Protonen fällt, wenn man beide als Punktteilchen modelliert und Maxwells Gleichungen anwendet. Es wird erklärt, dass die Quantenmechanik verhindert, dass das Elektron in das Protonen fällt, da die Unsicherheit der Position und der Impuls des Elektrons die Kollapseinheit verhindert. Es wird auch die Bedeutung der Masse des Protons im Vergleich zum Elektron diskutiert, die die Quantenunsicherheit reduziert. Der Absatz endet mit einer Erklärung der Koordinatensysteme, die für das Wasserstoffatom verwendet werden, insbesondere die sphärischen Koordinaten R, Theta und Phi.

10:02

📚 Wellenfunktion und Wahrscheinlichkeitsdichte

In diesem Absatz werden die grundlegenden Konzepte der Quantenmechanik wie die Wellenfunktion PSI, die Wahrscheinlichkeitsdichte und die reduzierte Planck-Konstante h-bar vorgestellt. Die Wellenfunktion ist eine komplexe Funktion von Raum und Zeit, die die Wahrscheinlichkeitsdichte beschreibt, indem sie die Amplitude des Wellenfunktions quadriert. Die reduzierte Planck-Konstante ist ein fundamentales Element in der Quantenmechanik, das die Beziehung zwischen Energie und Frequenz, Impuls und Raum definiert. Der Absatz führt auch die Schrödinger-Gleichung ein, die die Beziehung zwischen dem Hamilton-Operator und der Wellenfunktion beschreibt und die Grundlage für die Berechnung von Energiezuständen bildet.

15:04

🔗 Energieeigenzustände und Hamilton-Operator

Dieser Absatz erklärt die Energieeigenzustände und wie sie mit dem Hamilton-Operator in Verbindung stehen. Es wird gezeigt, dass die Anwendung des Energieoperators auf einen Energieeigenzustand die Wellenfunktion nur überall im Raum skaliert. Dies wird mit dem klassischen Eigenvektor-Eigenwert-Problem aus der linearen Algebra verglichen. Der Absatz führt dann den Hamilton-Operator für das Wasserstoffatom ein, der die kinetischen und potentialen Energien des Elektrons umfasst. Die kinetischen Energien werden durch den Impulsoperator dargestellt, der aus der klassischen Physik bekannt ist, und die potentielle Energie wird durch die Coulomb-Potentiale des Elektrons und Protons beschrieben.

🧲 Hamilton-Operator und Laplace-Operator

In diesem Absatz wird der Hamilton-Operator für das Wasserstoffatom vollständig formuliert, der sowohl die kinetischen als auch die potentiellen Energien des Elektrons berücksichtigt. Es wird erklärt, dass die Lösung der zeitunabhängigen Schrödinger-Gleichung die Bestimmung der Energieeigenzustände und der entsprechenden Wellenfunktionen erfordert. Der Laplace-Operator wird in sphärischen Koordinaten geschrieben und in die Gleichung eingesetzt, um eine dreidimensionale partielle Differentialgleichung für die Wellenfunktion PSI zu erhalten. Dies ist ein komplexer, aber fundamentaler Schritt in der Lösung der Schrödinger-Gleichung für das Wasserstoffatom.

Mindmap

Keywords

💡Hydrogenatom

Ein Hydrogenatom besteht aus einem Protonen und einem Elektron. Im Grundzustand ist das Elektron so nah wie möglich am Protonen, bis die Quantenmechanik 'Quantenunschärfe' eintritt. Im Video wird das Verhalten des Elektrons im Hydrogenatom im Grundzustand und nach dem Absorption von Photonen diskutiert.

💡Quantenmechanik

Quantenmechanik ist eine Theorie in der Physik, die das Verhalten von Teilchen auf sehr kleinen Skalen beschreibt. Im Video wird gezeigt, wie die Quantenmechanik die Stabilität des Elektrons im Hydrogenatom erklärt, da es nicht in den Protonen fallen kann, sondern durch die Unschärfe der Wellenfunktion 'gefangen' bleibt.

💡Wellenfunktion

Die Wellenfunktion ist eine komplexe Funktion, die die Quantenzustände eines Teilchens beschreibt. Im Video wird die Wellenfunktion verwendet, um die Position des Elektrons im Hydrogenatom zu beschreiben und wie sie durch die Absorption von Photonen verändert wird.

💡Schroedingersche Gleichung

Die Schroedingersche Gleichung ist eine zentrale Gleichung in der Quantenmechanik, die die zeitabhängige Entwicklung der Wellenfunktion eines Teilchens beschreibt. Im Video wird die Gleichung verwendet, um die Energiezustände des Elektrons im Hydrogenatom zu bestimmen.

💡Energieeigenzustände

Energieeigenzustände sind Zustände, in denen ein Teilchen eine bestimmte, diskrete Energie hat. Im Video werden diese Zustände verwendet, um die verschiedenen Energieniveaus des Elektrons im Hydrogenatom zu beschreiben, die durch das Absorbieren von Photonen erreicht werden können.

💡Quantenunschärfe

Die Quantenunschärfe ist ein Grundprinzip der Quantenmechanik, das besagt, dass die Position und der Impuls eines Teilchens nicht gleichzeitig genau bestimmt werden können. Im Video wird dies verwendet, um zu erklären, warum das Elektron nicht in den Protonen fallen kann.

💡Hamilton-Operator

Der Hamilton-Operator ist in der Quantenmechanik die Energie des Systems, geschrieben in Form von Position und Impuls. Im Video wird er verwendet, um die Schroedingersche Gleichung für das Hydrogenatom zu konstruieren und die Energiezustände zu berechnen.

💡Laplacian

Das Laplacian ist eine Differentialoperator, der die Konvexiät einer Funktion in drei Dimensionen misst. Im Video wird es verwendet, um den kinetischen Energie-Operator in der Schroedingerschen Gleichung zu definieren, was wichtig ist, um die Bewegung des Elektrons im Hydrogenatom zu beschreiben.

💡Reduzierte Planck-Konstante

Die reduzierte Planck-Konstante, h-bar, ist ein fundamentales Maß in der Quantenmechanik, das die Beziehung zwischen Energie und Frequenz sowie zwischen Impuls und Raum definiert. Im Video wird h-bar verwendet, um die Gleichungen in der Schroedingerschen Gleichung zu skalieren.

💡Sphärische Koordinaten

Sphärische Koordinaten sind ein Koordinatensystem, das für Probleme mit kugelsymmetrischer Geometrie verwendet wird. Im Video werden sphärische Koordinaten verwendet, um die Laplacian und die Wellenfunktion des Elektrons im Hydrogenatom zu beschreiben.

Highlights

Quantum fuzziness prevents the electron from collapsing into the proton in a hydrogen atom.

Electron transitions to higher energy states upon photon absorption, exemplified by the 2p0 state.

Metastable states, like the 2p0, are temporary and the electron returns to the ground state, releasing a photon.

The electron's angular momentum is demonstrated in the 2p1 state, showcasing quantum mechanics' intricacies.

The paradox of the electron not falling into the proton is explained by quantum mechanics' uncertainty principle.

Localization of a quantum particle increases its momentum, preventing it from collapsing due to energy requirements.

The reduced mass of the electron is used in the Hamiltonian for the hydrogen atom, accounting for the proton's finite mass.

Spherical coordinates are chosen for the hydrogen atom due to its spherical symmetry.

The wave function, probability density, and reduced Planck's constant are fundamental to quantum mechanics.

The Schrödinger equation is the key to understanding the relationship between energy, momentum, space, and time in quantum systems.

Energy eigenstates, or stationary states, are solutions to the time-independent Schrödinger equation.

The Hamiltonian operator for the hydrogen atom combines kinetic and potential energy terms.

The quantum mechanical momentum operator is derived from the classical momentum, using the reduced Planck's constant.

The potential energy operator in the Hamiltonian is based on the Coulomb potential between the electron and proton.

The time-independent Schrödinger equation is solved for energy eigenstates to find the allowable energy levels of the hydrogen atom.

The Laplacian in spherical coordinates is used to transform the Schrödinger equation into a solvable form.

The solution to the Schrödinger equation for the hydrogen atom reveals the quantum mechanical behavior of electrons.

Transcripts

play00:02

foreign

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look at this beautiful hydrogen atom in

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the ground state there's one proton one

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electron and the electron is as close as

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it can be to the proton until Quantum

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fuzziness kicks in and the electrons

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kind of in this wave function of

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positions and you don't know exactly

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where it is but it's something like this

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let's shoot a photon at this and see

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what happens

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look at this it's a two zero zero State

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very nice so now the electron is a bit

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farther out a bit less bound to the

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proton in a higher energy State relative

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to the ground state but be careful this

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is only metastable it's going to pop

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back down soon so any minute now it's

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going to pop into the ground state

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oh there it goes and look we got our

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Photon back did you see that flash of

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light

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conservation of energy very nice let's

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put another Photon into it and see what

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happens

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hey that's a two one zero State nice you

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know that one has some angular momentum

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oh there it goes

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let's take a moment to meditate on this

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situation

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[Music]

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foreign

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[Music]

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[Music]

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we'll Begin by examining our atom in its

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most relaxed form this dazzling little

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pattern is one of Nature's most abundant

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most ancient motifs

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but there's a deep mystery here why is

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it that the electron doesn't just fall

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into the proton

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if you model the electron and the proton

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as Point particles and apply Maxwell's

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equations you'll find that the electron

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will radiate out its energy and will end

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up falling into the proton in just a few

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nanoseconds

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but there's hydrogen out in space that's

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like billions of years old so clearly

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our math is a little bit off because

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hydrogen actually doesn't Decay

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instantly so what is it that stops the

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collapse

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have you ever tried to catch a Quantum

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particle

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imagine you have one and you've caught

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it you're pinching it between your

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finger and your thumb and you squeeze it

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really tight so you know just exactly

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where it is you know it's positioned

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with perfect precision

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oh well by quantum mechanics now you no

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longer know its momentum and so it

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escapes

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in quantum mechanics you actually can't

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perfectly localize a single particle

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you can try but it takes a lot of energy

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and the tighter you squeeze it the more

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you localize it the more energy it takes

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if you think about it a proton is

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pulling in the electron the electrons

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this Quantum particle it wants to

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collapse all the way but eventually

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there's a point where the quantum

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fuzziness makes it so that the

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uncertainty and momentum keeps the thing

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from falling all the way in

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and so you see hydrogen is not just an

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atom it's also this portal between the

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world of experiment and the very strange

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and unusual world of quantum mechanics

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that bubbles up into our world wait hold

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up so the electron is a Quantum particle

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and it's all fuzzy but the proton is

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just this point-like thing how does that

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make sense

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well it's because the proton is about

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1836 times as massive as the electron so

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just to put this into perspective the

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difference in Mass between an electron

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and a proton is the difference between

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an elephant

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and 1836 elephants so the proton is very

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very massive because it's so much more

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massive it's less fuzzy it is still

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fuzzy if you look very closely at it

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it's fuzzy but it's much less fuzzy

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because there's this inverse

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relationship between distance and mass

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when it comes to quantum mechanics

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because the proton is so much more

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massive than the electron we can do all

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of our analysis by assuming that the

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proton will be at the center of our

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coordinate system and that it doesn't

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move it just stays put and the electron

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does whatever quantum mechanical cloudy

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wavy stuff it does okay all right let's

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talk about coordinates normally I like

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to use Cartesian coordinates X Y and Z

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but because of the nature of this

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problem it has a spherical Symmetry and

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so spherical coordinates fit like a hand

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in a glove to this problem so we're

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going to use these the coordinates R

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Theta and Phi one thing I have to point

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out I got to be careful here so normally

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I use Theta as the angle around the

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longitude like the azimuthal angle and I

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used Phi for the elevation angle but for

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whatever reason physicists working on

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the hydrogen atom always use the other

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way of defining Theta and Phi and so I'm

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going to go along with that convention

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but just be aware this is a little bit

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different than the convention that I

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normally use so just to be really clear

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Theta is actually going to be our

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elevation angle so that's going to be

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the angle that starts off at zero on the

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North Pole and then goes down to Pi or

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180 degrees at the South Pole and then

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Phi is going to be our azimuthal angle

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so that's the angle that's going to go

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around the equator zero at the Prime

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Meridian and then you know it goes

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around a full 360 or full 2 pi

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okay so now that we've defined our

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coordinate system let's define some of

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the most important things in quantum

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mechanics the first thing is the wave

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function so the wave function is this

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complex valued function that's a

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function of both space and time so the

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wave function is given the symbol PSI

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and PSI depends in this case on R Theta

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Phi and time

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closely related to the wave function is

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the probability density that is the

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thing that if you integrate over some

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volume you get the probability that the

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particle is going to be in that volume

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the probability density is just the

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amplitude squared of the wave function

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when you take the amplitude squared of a

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complex number you get a real number so

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the probability density is a real valued

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function and it's also a function of

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space and time although as we'll see

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when we solve any dragon States it's

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just a function of space all right and

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finally the reduced Planck's constant

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this number h-bar you see this

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everywhere in quantum mechanics it's

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absolutely ubiquitous it's a measurable

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quantity it has about the value of

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1.05457 times 10 to the minus 34 Joule

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seconds this is a very mysterious number

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it is what it is and no one knows why it

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is it just is and so you'll see this in

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many of our equations today it defines

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the relationship between energy and

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frequency and momentum and space and all

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kinds of stuff sort of the quantum scale

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of angular momentum or action and by the

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way I should mention you know why they

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call it h bar it's actually plan's

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constant H divided by 2 pi why but so

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often you divide by 2 pi that people got

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tired of writing divided by 2 pi so then

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they just put a bar on the H now

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everyone knows that means divide by 2 pi

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so we want to figure out what is our

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electron up to what does it do and in

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order to do that we need an equation

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that lets us relate things like momentum

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and space and time

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and so what we're going to do is we're

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going to use the Schrodinger equation

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shown here the Schrodinger equation is

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just the idea that if the hamiltonian

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operator acts on a wave function that's

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the same thing as the energy operator

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acting on a wave function now there's a

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lot of confusion when people first see

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hamiltonian operator they're not sure

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what that is because it's just a thing

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named after some guy so who knows what

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it is well what it is is the energy

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written in terms of position and

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momentum and we'll see in a moment

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exactly how to construct the hamiltonian

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for the hydrogen atom

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the energy operator is in quantum

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mechanics it's defined as I H Bar times

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partial PSI partial T so in other words

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you take the partial derivative of the

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wave function in time then you rotate it

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90 degrees in the complex plane by

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multiplying by I and then you multiply

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it by that Quantum scale parameter h-bar

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now if you look at this you might be

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wondering why is this the energy

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operator where does this come from and

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the answer is today we're just going to

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take this as one of our principles as

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one of our assumptions that we're going

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to use to build up this theory if you're

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interested more in the nature of the

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energy operator I'd recommend the book

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quantum mechanics and path integrals by

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Feynman and hibs this book constructs

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quantum mechanics from a pretty

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intuitive starting point well relatively

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for quantum mechanics and and then they

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show that you can basically derive all

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of this Schrodinger wave equations from

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path integrals now the problem with path

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integrals is they're impossible to work

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with but they're very nice to imagine so

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if you want to learn more about why the

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energy operator is what it is check out

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that book but today we're just going to

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take the energy operator for granted and

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we're going to continue forward now when

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we solve the Schrodinger equation we're

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not just interested in every possible

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wave function as a function of space and

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function of time we're actually

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particularly interested in these things

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called Energy eigenstates they're also

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known as stationary States I like to

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think of them as resonant mode although

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that's maybe kind of an analogy but I

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think it's a good one

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so an energy eigenstate is a wave

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function that doesn't move except it

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just rotates in the complex plane

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so in other words you can break it up so

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the wave function is a function of space

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and time

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can be thought of as the wave function

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as a function of space

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times this time parameter which just

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swings around in the complex plane and

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the frequency of how much it swings

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around has to do with the energy of the

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wave function

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so when we solve for the time

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independent Schrodinger equation what

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that means is we want to figure out what

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are all the patterns what are all the

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different wave functions as a function

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of space and then what are the

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corresponding energy levels by the way

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the energy levels are also called Energy

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eigenvalues

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the deal with all this eigen stuff

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anyway well if you've studied linear

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algebra then you'll be familiar with

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eigenvector and eigenvalue problems

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normally you'll have some kind of linear

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transformation and then there are

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specific vectors that are just uniformly

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scaled by that transformation and the

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amount to which they're scaled is the

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eigenvalue and the vectors themselves

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are eigenvectors and eigen I think it

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comes from some German word meaning own

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or self or like related to the thing

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it's confusing terminology admittedly

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but let's just apply the energy operator

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to an energy eigenstate and see how we

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can draw that parallel between

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eigenvector eigenvalue problems and this

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whole thing about eigenstates if we

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apply our energy operator to psi so we

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do I H bar partial PSI partial T and we

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substitute in our wave function which is

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our energy eigenstate where we have a

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spatial part and a time part and then

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we'd work out the derivatives what we

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find is that the energy operator

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basically amounts to just scaling the

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wave function by a constant everywhere

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in space

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and so you'll notice that this seemingly

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simple looking equation E hat PSI equals

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e PSI it's actually pretty profound and

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this should look a lot like your classic

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you know Matrix times eigenvector equals

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eigenvalue times eigenvector equation

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from linear algebra by the way that's

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not a coincidence if you've studied

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structural engineering and you've

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calculated resonant modes and

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frequencies you'll see there's really a

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one-to-one parallel between that

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situation and what's going on here today

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okay so just to recap the time dependent

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Schrodinger equation that is the general

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the real for real Schrodinger equation

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is the equation that the hamiltonian

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operator acting on a wave function is

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the same as the energy operator acting

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on a wave function and that lets us

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relate momentum and space and time and

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we can derive the governing equations of

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our wave function

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if we restrict our attention to solving

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for these energy eigenstates which you

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can imagine is resonant modes or the

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ways in which the equation rings then we

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end up with the time independent

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Schrodinger equation in which the energy

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operator is replaced by a constant that

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constant of course depends on the

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particular energy eigenstate we're

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looking at some of them will have higher

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energies some of them will have lower

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energies but in any case we can regard

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that energy level as an eigenvalue of

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the hamiltonian operator acting on our

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wave function

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let's construct the hamiltonian for the

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hydrogen atom to do that we need to add

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the electrons kinetic and potential

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energy

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first let's start with the kinetic

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energy

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from classical non-relativistic physics

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we know that the kinetic energy T is

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equal to one-half MV squared where m is

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the mass of the particle and V is the

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velocity we also know from classical

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physics that momentum p is mass times

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velocity

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therefore if you just rearrange those

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equations you can prove to yourself that

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the kinetic energy is the momentum

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squared divided by twice the mass

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and in quantum mechanics we're going to

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use that exact same idea except we're

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going to make the momentum a Quantum

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thing how do we do that well we use the

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quantum mechanical momentum operator

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so the momentum operator P hat acting on

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the wave function PSI is negative i h

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Bar times the gradient of PSI

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now if we use our formula from classical

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physics that the kinetic energy is

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momentum squared divided by twice the

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mass then we can derive the quantum

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mechanical kinetic energy Operator by

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applying the momentum operator twice and

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dividing by twice the mass

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when we do that we find that the kinetic

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energy operator t-hat applied to a wave

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function PSI gives you negative H bar

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squared over 2m times the laplacian of

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PSI

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and what that means intuitively is that

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if you're going to take the kinetic

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energy of a wave function you look at

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its laplacian the laplacian is basically

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the concavity in three dimensions it's

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like a second derivative but adding up

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along all the different second

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derivative and X Plus second derivative

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and Y plus second derivative and z and

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then you multiply that concavity by H

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bar squared over 2m and then you take

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the minus sign of that

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so you know earlier we were talking

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about how it takes energy to localize a

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particle the more you squeeze it the

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more it sort of pushes back well we can

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mathematically encode that in this

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equation with the kinetic energy

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operator right because you think about

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it the more you pinch a particle the

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more you're increasing its laplacian you

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know the laplacian in a way is sort of

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the extent to which the wave function is

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pinched right it's the Divergence of the

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gradient so the more you pinch it the

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more this t-hat term increases

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now if we look at the potential energy

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from the electron and proton coulomb

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potential so in other words just the

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regular old static electricity Coulomb's

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law we can see that the potential energy

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operator V acting on our wave function

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PSI is just the Classic minus Elementary

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charge squared over 4 pi times the

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permittivity of free space times the

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radial coordinates all acting on our

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wave function PSI

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and so what that means is that there's

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going to be a potential energy term in

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our equation that drops off as 1 over r

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but notice there's a minus sign on this

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potential energy and so actually a

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bigger magnitude means it's more

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negative

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negative energy in this context just

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means that it's less than zero so if the

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electron and proton are infinitely far

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away let's call that zero then the

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coulomb potential is negative because it

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represents a kind of energy dead you'd

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have to put energy into the hydrogen

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atom in order to get the electron out

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and so actually this one over R scaling

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of the electrostatic potential is going

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to tend to pull the electron in to the

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proton

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and so when we add the kinetic and

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potential energy terms together in our

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hamiltonian what we're describing when

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we do that is that balance of energies

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we were talking about earlier between

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the electron getting pulled into the

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proton but also that quantum mechanical

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fuzziness that kinetic energy keeping

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the electron from falling all the way in

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and so we can finally write our

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hamiltonian operator H hat acting on PSI

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as negative H bar squared divided by

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twice the mass times the laplacian of

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our wave function minus the fundamental

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charge squared divided by 4 Pi

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permittivity of free space r times PSI

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okay maybe it looks like a lot if this

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is the first time you've seen it but all

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that is to say the energy of the

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electron has a kinetic term and it has

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an electrostatic potential term

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now something I should mention here is

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that we want to actually use something

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called the reduced mass of the electron

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so this is basically the same thing as

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the electron Mass it's like a little

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tiny bit less like a part in a thousand

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less kind of thing and what that does is

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it lets us account a little bit for the

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fact that the proton actually has finite

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Mass it's not infinitely massive this

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idea comes from orbital mechanics I

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believe is where this first comes from

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but for our purposes today basically the

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main advantage is it lets us replace the

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letter M with the letter mu because

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we're going to need M later on when we

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get to the magnetic quantum number

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all right well now that we have our

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hamiltonian we can plug it into the time

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independent Schrodinger equation that is

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H hat PSI equals e PSI where e is the

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energy eigenvalue and PSI is an energy

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eigenstate

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let's massage this equation a little bit

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we'll move the E side term on over to

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the left side of the equation we'll

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cancel out some minus signs and we get

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this pretty looking equation that the

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laplacian of PSI plus 2 mu over H bar

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squared times e squared over 4 Pi

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Epsilon not R plus e times PSI equals

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zero

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so up until this point we've used

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physics and this idea of energy

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operators and Schrodinger equation and

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hamiltonian so we've compiled this

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equation but now solving this equation

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is an exercise in math

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because we can just look at it as a

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three-dimensional partial differential

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equation and ask what are the functions

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PSI that satisfy this equation

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So to that end the first thing that we

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should do is write out the laplacian in

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terms of partial derivatives of PSI with

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respect to R Theta and Phi

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now here's the thing uh so earlier I

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mentioned that using spherical

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coordinates was going to help us out

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because of the spherical nature of the

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problem and that is true spherical

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coordinates are very nice trust me we do

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want to use them but there's one way in

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which they're not so nice and that is

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when you write out the laplacian it's

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quite an expression anyway I'm not going

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to go into the whole derivation of this

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now but if you just look up laplacian

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written in spherical coordinates you'll

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see this expression it's a bit

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complicated but it is what it is you

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know no matter how fun it is it is what

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it is okay now all we have to do is take

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our expression for the laplacian and put

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it into that equation and what we end up

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with is a three-dimensional partial

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differential equation for PSI as a

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function of the variables R Theta and

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Phi

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wow look at this thing oh what a mess

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but there it is this is a beautiful

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equation in a way

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so let's solve it let's solve it for PSI

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how hard can it be

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