th dimension of inverse of distance, represents a radial-space frequency. We believe that the phase factor of the oscillatory function is the key point to answer the questions formulated preously. As we will see soon, this phase factor is directly related to the Heisenberg uncertainty principle and the quantization of the angular momentum.
For fixed values of the parameter (), the function oscillates between zero and one, while the function oscillates between zero and the classical Coulomb potential energy. The equation (1), tell us that when, , the new potential function becomes equal to the classical Coulomb potential.
However, we need to observe that if we make, we have for all values of the distance between the proton and the electron in the hydrogen atom. This implies that the linear momentum of the electron is null. That is, the electron is at rest in the LFR (Laboratory Frame of Reference). This condition strongly contraries one of the basilar principles of the quantum mechanics, the Heisenberg uncertainty principle That is, if we make the uncertainty of the linear momentum, we have , and the radial position of the electron becomes completely undetermined. On the other hand, if we make, we have, making the kinetic energy of the electron infinitely large [2-4]. This clearly shows the inadequacy of the Coulomb potential to describe the interaction between the proton and the electron in the hydrogen atom, except at particular points of the space in the vicinity of the nucleus of the atom. The phase factor of the oscillatory function selects only specific points of the Coulomb potential, making it to satisfy the Heisenberg uncertainty principle only at points, where the condition is satisfied. This constitutes a quantized relation between the normal and the reciprocal space.
Looking for the determination of the parameter, we will make use of the quantum-mechanical analogue of the virial theorem and the de Broglie relation between the linear momentum of the particle and the wave number. With this procedure, we are making use of well known quantum concepts to determine the phase factor of the new potential. The quantum analogue of the virial theorem can be set in the form 
and the required de Broglie relation is
To facilitate the application of equation (1), it turns out to be convenient that the parameter may be expressed in terms of known quantities such as, the charge and mass of the electron and some physical constants. With the use of equations (1) and (3), the average kinetic energy of the electron in the hydrogen atom is found to be expressible as
With the use of equation (4) it follows that
We will select the desired particular points along the Coulomb potential, observing that every time the product satisfies the quantization relation,
the Coulomb potential becomes equal to the oscillatory potential and the equation (6), may be written as
The equations (7) and (9) become consistent if we set and
what permit us to rewrite the equation (9) as
Comparing the equations (7) and (11) we can identify the space-frequency as a quantized quantity given by
In the hydrogen atom we have and, in its ground state, The quantity may be identified as the first Bohr radius Å of the electron. The equation (12) may be rewritten as
This implies that for two atomic bound particles, such as the proton and the electron in the hydrogen atom, the average value of the linear momentum of the electron is also a quantized quantity
Using equation (13), the new potential function may be rewritten as
We are naming this potential by Quantum Oscillatory Modulated Potential-QOMP; because, it is quantized, it oscillates with k-space frequency, and it is partially modulated by the classical Coulomb potential. Using the condition given by equation (7) and the equations (1) and (5), the average total energy of the electron with respect to the nucleus is
Taking the average value as given by equation (10), the energy of the electron becomes quantized and may be written as
as would be expected, it is the same relation as obtained with Bohr theory and also with the solution of the time-independent Schroedinger wave equation for the hydrogen atom when the Coulomb potential is used. But, differently from these two theories, that in different circumstances, make explicit use of the quantization of the angular momentum to obtain the total energy of the electron, in this work, the same result is achieved without making explicit use of this concept. Implicitly, the quantization of the angular momentum is contained in the phase factor of the oscillatory function, equation (7).
The figure 1 shows a graphic of the potential. As shown in the figure, the electron in the hydrogen atom occupies the first well with position and total energy satisfying the equations (10) and (17), respectively. The figure 2 shows the graphics of for and 3. The values of the energies shown in the graphic determined by the positions of the electron are, respectively, −13.6 eV, −3.4 eV and −1.5 eV. The same results are predicted by equation (17) [4,5].
The new potential present us with several interesting features: 1) Its waving character shows a sequence of periodic wells and barriers with variable depth and height; 2) The first well is at the position most likely to be occupied by the electron in the ground state of the atom; 3) The quantization of the energy may be attributed to the existence of concentric quantum shells, formed by wells and barriers, created by the interaction of the nucleus of the atom and the electron; 4) According to this potential, the electron bound to the nucleus can only jumps from one quantum well to another by tunneling through finite potential barriers. The tunneling effect (a purely quantum mechanical phenomenon) now appears naturally as necessary condition for emission or absorption of energy (light) by the atom; 5) Another new interesting aspect of the oscillatory potential, observed in the figure 2, and predicted by equations (13) and (14) is the fact that the de Broglie wavelength associated to the electron is equal to the first Bohr radius of the electron in the hydrogen atom. Thus, the average distance between the proton and the electron, for any excited state of the atom, may be written as
Or, equivalently, in terms of the de Broglie wavelengths we may write
Figure 1. The Coulomb potential U(r)Coul and the quantum oscillatory modulated potential U1(r), showing the position and energy of the electron in the ground state of the hydrogen atom. The positions R1 and R2 are classical turning points for the electron.
Figure 2. The Coulomb potentials U(r)Coul, the quantum oscillatory modulated potentials Un(r) and the energy levels and positions of the electron in the hydrogen atom for n = 1, 2 and 3.
This result is completely different from that predicted by the quantization rule for each allowed orbit for the electron, as postulated by Louis de Broglie, to explain the quantization of the angular momentum of the electron in the Old Quantum Theory [5,6].
Figure 2 shows that the averaged positions occupied by the electron in the first three quantum wells of, and are, respectively, Å, and In this work we are arguing that the Coulomb potential is not totally appropriated to describe correctly the potential interaction between two microscopic electric charges. However, as is well known, the solution of the time independent Schroedinger wave equation predicts correctly the quantization of the angular momentum and energy of the electron, when Coulomb potential is used in the Hamiltonian of the protonelectron system. This occur because, in the solution of the radial part of the Schroedinger differential wave equation, without noticing it, we are making use the quantization rule for the phase factor of the oscillatory function of the new potential. That is, implicitly, we are making and, consequently, selecting only the points of minima of the new potential, where both interaction potentials are coincident, see figure 2. In these selected points the Coulomb potential satisfies the Heisenberg uncertainty principle. In terms of a mathematical treatment, the quantization of the phase factor allow us to see that the Coulomb potential is a particular case of the oscillatory potential, by transforming the Schroedinger radial differential equation
obtained with the use of the Quantum Oscillatory Modulated Potential in the Hamiltonian of the protonelectron system into the simpler and familiar radial differential equation [4,5]
obtained with the use of the classical Coulomb potential, with the condition or The solution of equation (21) is well known and it is found in many books of modern physics literature [4-7]. Its solution shows that the total energy of the electron in the hydrogen atom is the same as predicted by equation (17). Up to this point we can also state that the Coulomb potential is restricted to describe correctly the interaction between two microscopic electric charges only at particular points of the space around nucleus of the atom, points where the quantization relation and, consequently, the Heisenberg uncertainty principle are satisfied.
3. A New Electric Interaction Microscopic Force
The electric force between two macroscopic electric point charges and separated by a distance is given by the well known classical Coulomb formula
which is perfectly valid as far as we consider the two charges built up of a very large number of protons or electrons, but still considered as point charges. However, the electric force between two microscopic charges such as proton-proton, proton-electron, or electron-electron, originated from the new potential function, has the form of a wave packet, written as
The forces oscillate with the same k-space frequencies. For the hydrogen atom, figure 3 shows a graphic of, as predicted by equation (23). Since this force is the gradient of the energy function, which presents a minimum at position, it becomes null at this point. We must observe that with the use of the classical Coulomb potential this situation never occurs, the interaction force between the proton and the electron is always attractive. The acceleration due to the electric force being null at this position, eliminates the argument or defiance against the Classical Laws of the Electrodynamic that an electron revolving the nucleus of the atom, lose energy by radiation [8-10]. The force being null at the equilibrium position, means that the electron cannot be orbiting the nucleus of the atom as predicted by Bohr theory. Thus, according to the QOMP, the angular momentum of the electron in its ground state is null, in agreement with the prediction of the Schroedinger radial differential wave equation (21). On the other hand, the electron cannot be a static physical object due to the Heinsenberg uncertainty principle. The angular moment of the electron being null implies that the movement of the electron, inside a quantum well must be radial, bouncing back and forth, confined by two potential barriers.
This argument is reinforced by observing that in figure 3, the interaction force between the proton and the electron is repulsive to the left of the position and attractive to the right of this position. That is, the electron is always being pushed towards the equilibrium position, acting like a harmonic oscillator. However, being accelerated towards the equilibrium position, again, the electron should lose energy by radiation and the problem of stability of the atom continues to be unexplained. The stability of the atom will be object of a deeper discussion in the second paper of this series of work. Figure 4 shows the behavior of the electric forces for and 3. The graphics show that the waving character of interaction electric force decreases when increases, in agreement with the Bohr correspondence principle. The reasons for this behavior are two: 1) The destructive interference of the waving pattern of the individual charges, protons and electrons occur because, when macroscopic charges3 are built up, these particles do not occupy the same position in space and the waving pattern of the force must be destroyed by an interference process; 2) The actual measurements of the interaction
Figure 3. The interaction oscillatory force F1(r), the quantum modulated potential U1(r) and the Coulomb potential U(r)coul in the ground state of the hydrogen atom. The figure also shows that the force is null at the equilibrium position r1.
Figure 4. The Coulomb force F(r)coul and the interaction oscillatory forces Fn(r) between the proton and the electron in the hydrogen atom, for n = 1, 2 and 3.
force between two macroscopic particles are usually performed, using large ionized atoms, for which the escaped electrons come from outer shells of the atoms, making the new electric force to approximate quickly to the classical Coulomb force as indicated in figure 4.
We can summarize this work as follows: For the hydrogen atom, the oscillatory potential function is able to predict correctly the values of the total energy and position of the electron in the atom, without the necessity of solving the time-independent Schroedinger wave equation. In addition, it shows several peculiarities of the hydrogen atom, such as: The existence of quantum wells and barriers, forming closed shells around nucleus of the atom. These wells constitute the most probable positions for the electron to occupy when moving around the nucleus of the atom; The emission or absorption of energy by the atom happens when the electron moves from one state of equilibrium to another by tunneling through these potential barriers created by the oscillatory potential; The new potential shows that the electric force between the proton and the electron oscillates, presenting negatives and positives peaks, the positive peaks represent regions where the interaction force between the proton and the electron is repulsive and the negative peaks where it is attractive, that is, the electron is always been pushed to the equilibrium position, which is a necessary condition for the stability of the atom. The new potential predicts that de Broglie wavelength associated to the electron is equal to the radius of Bohr, what is quite different of the condition postulated by Louis de Broglie for the quantization of the angular momentum of the electron in the Bohr Old Quantum Theory. According to the new potential, the electron is not orbiting the nucleus of the atom but oscillating radially, confined by two potential barriers. Whats more, this work presents strong evidences that the Coulomb potential function is not adequate to describe the correct interaction between two microscopic electric charges, because, except at particular points around the nucleus of the atom, it is in disagreement with one of the basic principles of quantum mechanics-the Heisenberg uncertainty principle. The new potential is much more informative than the classical Coulomb potential and more appropriated to accomplish the function for the interaction between two microscopic electric charges.
1The stability of the atom will be treated in the second paper of this series.
2This subject will be considered in the third paper and, for an uncharged particle, possessing an electric dipole moment, the subject will treated in the fourth paper of the series.
3A macroscopic charge of 1 μC = 1 × 10−6 C, contains about 1013 electronic charges.