No reason one cannot have double-well structures: With MBE growth, can control well thicknesses and spacings at atomic scale.

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The story so far: Can use semiconductor structures to confine free carriers electrons and holes. Can get away with writing Schroedinger-like equation for Bloch envelope function to understand, e.g., -confinement and -subband energies in quantum wells. Excitons, bound e-h pairs, can show profound confinement effects, detectable through optical properties. Again, energy scales are set by boundary conditions on envelope wavefunctions at interfaces.

Double wells No reason one cannot have double-well structures: E c B A B A B E v With MBE growth, can control well thicknesses and spacings at atomic scale. Can place wells close enough to allow controlled overlap of bound state wavefunctions.

Coupled wells Consider just electrons in conduction band: E E Effective Schroedinger: * m = + + ε Assume wavefunction is l.c. of isolated well states: a a + =

Coupled wells Overlap matrix element = H = = = where the well states satisfy, * * E m E m = + = + Assumes identical isolated wells. Resulting Schr. Eqn.: = + + 0 0 0 * 0 a a E E ε ε Define 0 = =

Resulting states: Energy eigenvalues are ε = E + 0 +- No big surprise: bonding and antibonding states in, while still free in x and y. One could just as easily imagine making a real-life Kronig-Penney system of wells. Such a system is called a superlattice: Resulting bands of well states are called minibands. Precise control of miniband structure is possible.

Superlattices Start with a regular superlattice of identical wells. Same tight-binding / molecular orbital theory approach works well here. S equivalent to alpha, T equivalent to beta, q runs from /Nd to N-/Nd. Result is a miniband. Image from Weisbuch

Minibands and Band Gap Engineering Density of states for simple superlattice in tight-binding approx.: m υ ε = N π arccos * ε Ei T i S i Image from Weisbuch By playing with superlattice, can tune miniband structure.

Quantum cascade lasers Why would you want to tune miniband structure? Engineering of optical properties! Image from Bell Labs

0d structures: quantum dots What happens when we confine electrons in the x and y plane as well as the direction? When confinement is ~ Fermi wavelength of carriers, will see discrete single-particle states. How do we make such structures? Physical or electrostatic confinement, often starting from a deg confined in a quantum well or single interface. Why are they interesting? Controlled environment for studying fundamental manybody physics. Possible utility for future technologies quantum computers? Charge sensors?

Examples of quantum dots Image from Kouwenhoven/Marcus Physically confined GaAs deg electrostatically confined GaAs deg CdSe nanocrystal

Quantum dots - artificial atoms Just as -confinement from band structure leads to effective Schr. Eqn. for Bloch envelope function in -direction, lateral confinement does same in transverse directions. Assume some form for confining potential and solve: result are discrete bound single-particle states and energy spectrum orbitals. For confinement with high symmetry, get easy-to-understand spectrum classical periodic orbits, easily identifiable quantum numbers. For nonsymmetric b.c., get complicated spectrum classical chaotic motion. How are these bound states filled? Aufbau process, with exceptions, just as in real periodic table.

Example: circular dot from deg Common model: d harmonic oscillator, natural frequency ω. Quantum numbers: n = principle quantum number l = orbital angular momentum in plane s = spin = / s = -component of spin Energy spectrum: E n l, = n+ l + ω Include magnetic field: where E / n, l = n+ l + ω + ωc ω c eb m * 4 cyclotron frequency l ω c

What do wavefunctions and spectrum look like? Images from Kouwenhoven Magnetic field splits states by l value. Magnetic field shrinks wavefunctions.

How are they probed? Optical spectroscopy Microwave spectroscopy Transport spectroscopy. Transport spectroscopy relies on moving charges onto and off dot. We ll learn more about the details next week. For now, consider the following cartoon: discrete dot states source drain Charge can only flow well from source to drain if there is a dot level energetically degenerate with µ of source and drain. Can shift dot levels µ by capacitive coupling with gate electrode.

Classical Coulomb Blockade discrete dot states source drain Spacing between dot states not just spacing between singleparticle dot levels! Coulomb interactions: some charging energy cost to put an additional charge on the dot. How much? Suppose total dot capacitance = C. Charging energy is then e /C. No quantum mechanics here true for metal particles, too. Need barriers, but not insurmountable ones.

Classical Coulomb Blockade So, total addition energy to drop another charge onto the dot at fixed conditions = E + e /C. Without this much energy available, no current may flow: Coulomb Blockade. Write total capacitance as: C = C + C + C s d g Dot energy: e N N0 + Cgg + U N = Enl B C N For a fixed g there is a value of N that is closest to the minimum energy. Assume sd is small. If g is varied, there is some value for which UN and UN+ are equal charge on dot can change.

Classical Coulomb blockade Result: ignoring E nl G e/c g Conductance is peaked as a function of gate voltage. Width of peaks is proportional to T. Classical charging energy E c = e /C. To see Coulomb blockade, need k B T << E c. g

Charging energies What are some reasonable values for E c? Suppose source/drain capacitances are small. For a metal nanoparticle disk 00 nm in diameter, separated by a nm SiO layer ε = 3.9 from a gate electrode. C = 36 af. E c =.89 x 0 - J ~ 4 K. Challenging to get E c values high enough to see Coulomb charging effects at room temperature.

Constant interaction model Precise interaction effects are more complicated than just a classical charging energy. Consider circular dot. One simple approximation: if electrons are being added to bound states with the same n, the energy differences between subsequent states are uniform for B=0. So, look at peak spacings in gate voltage. Whenever there s a change in the spacing at ero B, we re seeing a transition from one closed shell to the beginnings of a new shell. Result: magic numbers, just as in atomic shells.

Magic numbers and shell structure

ariations of peak energies with magnetic field Remember, for nice, round quantum dot, E / n, l = n+ l + ω + ωc 4 l ω c Orbital angular momentum couples to external magnetic fields. Can watch magnetic field dependence of Coulomb blockade peaks as a function of g, and confirm which peaks correspond to which states!

Filling the states what do we expect: Two electrons per orbital state pairs of peaks should correlate. Expect to see crossings as l states trade places energetically.

Does this simple picture work?

Hund s rule Constant interaction picture misses funny business at low fields. Hund s rule shows up here, just as in real atoms. Exchange energy electronic correlations beyond the simple constant interaction picture.

What about non-symmetric and chaotic dots? Can t analytically solve for energies and wavefunctions. Dependence of state energies on magnetic field and dot shape can be extremely complicated. General theory is possible to describe statistics of peak spacings, peak heights, field dependences, etc.

Summary: By tuning composition, can engineer bound state energies precisely. Through superlattices, can create impressive optical devices. Confinement in all 3d directions leads to discrete 0d states quantum dots. Coulomb blockade allows transport spectroscopy of states. Simple dots are laboratories for atomic physics. Complicated dots can actually be understood statistically.

Next time: Classical + semiclassical transport.