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Free and Bound Electrons, Dimensionality Effects
                             3.2.6 The Hydrogen Atom
                             The paradigm for the electronic states of a central symmetric potential is
                             the hydrogen atom since it consists of one proton in the nucleus sur-
                             rounded by one electron. It helps in understanding the principle of elec-
                             tronic states of atoms which is similar to the electronic states of defects
                             and traps for electrons in the semiconductor or even helps to understand
                             the formation of a band structure. We shall not go into details of the deri-
                             vation but we shall have a closer look at the form of the electronic states.

                Coulomb      The Coulomb potential of the proton is spherically symmetric in three
                Potential    dimensions, which means that it depends only on the distance r of the
                                                    2
                             symmetry center  U r() =  – e ⁄  r   (e is the unit charge). The best choice
                             to tackle the problem is spherical coordinates, with the radius vector r
                                                                                 θ
                                                             φ
                             given by its modulus  , the polar angle   and the azimutal angle  . The
                                              r
                             Hamilton operator thus reads
                                                       2      2
                                                      —   2  e
                                                H =  – ------∇ –  -----           (3.68)
                                                      2µ     r
                             To solve the Schrödinger equation we must write the  ∇ 2   in spherical
                             coordinates, which reads
                                        1 ∂    ∂    1    1  ∂  ∂   1  ∂ 2  
                                    2
                                  ∇ =   ----  r 2  +  ---- -----------  sin θ  +  --------------------  (3.69)
                                        r ∂   r ∂   r 2 sin θ θ  ∂ θ  sin θ∂φ 2
                                                          ∂
                                          r
                                                                      2
                                        2
                             Inserting (3.69) together with (3.68) and solving the respective
                             Schrödinger equation is beyond the scope of this book. We restrict the
                             discussion to an interpretation of the electronic wavefunction and an
                             illustration of the atomic orbitals.

                             The common approach to calculate the bound electronic states of the
                             hydrogen atom (energy E <  0  ) starts with a product trial function for the
                                                    (
                                                      ,
                             wavefunction ψ r() =  Rr()Y θφ)  . Then the Schrödinger equation sep-
                             arates into two eigenvalue problems, one for the radial motion (Rr()  )
                             and one for the angular motion (Y θφ,(  )  ). The solutions of the angular



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