Published 07.02.2003
THE NEW INTERPRETATION OF
PHOTOEFFECT
Ph.M. Kanarev
The Kuban State Agrarian
University, Department of Theoretical Mechanics
13, Kalinin Street, 350044
Krasnodar, Russia
E-mail: kanphil@mail.kuban.ru
Abstract: It has been disclosed that the equation
suggested by A. Einstein for the interpretation of photoeffect is a mathematical model of the law of formation of
the atom and ion spectra discovered in 1993.
Key words: energy, photon, electron, bond
INTRODUCTION
It is known that the most acceptable
interpretation of experimental dependencies of photoeffect has been suggested by A.
Einstein in 1905, and he got the Nobel prize for it [1], [2], [3]. He made it in the
absence of the law of formation of the atom and ion spectra. Now this law has been
discovered, and we can check correctness of its interpretation and the possibility of
deeper understanding of photoeffect [4], [5], [6], [7].
THEORETICAL PART
The mathematical model suggested by A.
Einstein for the interpretation of experimental dependencies of photoeffect has the
following form [3]
,
(1)
where is kinetic energy of the photoelectron emitted by
the photocathode; is energy of the photon, but it is not explained in
the papers, of which photon exactly [1], [2], [3], is the
photoelectron exit work is a constant, which does not depend on frequency [1], [2], [3].
The main experimental dependencies of photeffect are given in Fig. 1 [2].
|
Fig. 1. Dependence of photocurrent on
light intensity: a) at its constant frequency; b) at different frequency
Photocurrent takes place in the
photocathode-collector circuit. If the photocathode is exposed to monochromatic light (Fig. 1, a), the value of potential retarding the photoelectrons emitted by the photocathode
does not depend on light intensity. Light intensity increase increases photocurrent and
does not exert influence on the retarding potential value and, consequently, on kinetic
energy of the photoelectrons. If frequency of light, which strikes upon the photocathode,
is increased, the value of the negative potential retarding
the photoelectrons is increased (Fig. 1, b).
As the value of the retarding negative
potential is determined by kinetic
energy of the
electrons emitted by the photocathode under the influence of light illumination, it
results from the dependence shown in Fig. 1,b that kinetic energy of the photoelectrons emitted by them is increased
with the increase of frequency of the photons exposing the photocathode.
Let us try to find a connection of Einsteins equation (1)
with the mathematical model of the law of formation of the atom and ion spectra (2). We
have already shown that the mathematical model, which describes the spectra of the
multi-electron atoms and ions, has the following form [4], [10], [12]:
,
(2)
where is energy of the photon absorbed or emitted by the
electron; is ionization
energy of the electron; E1 is energy of the bond of the electron with the
atomic nucleus, which corresponds to its first energy level; is the main quantum number.
The correlation (2) appears from
experimental spectroscopy, thats why it is a mathematical model of the law of
formation of the atom and ion spectra. Einsteins equation (1) describes similar
process of photon absorption by the electrons. It affords ground for supposition of
identity of the equations (1) and (2) and
uniformity of their interpretation. It appears from the given equations
.
(3)
It means that if the electron loses bond
with the atomic nucleus, its kinetic energy is equal to energy of the absorbed photon. Then
.
(4)
It appears from this that energy value in
Einsteins equation (1) is ionization energy of the electron emitted by the photocathode
material. It appears from the equations (1) and (2) that
.
(5)
The new clarification: photoelectron exit
work is equal to
binding energy of electron when it is on a definite energy level in the atom
or the molecule.
Experimental investigations of
photoeffect are carried out usually with the photocathodes made of alkali metals [1]. For
example, it is known that the work of the photoelectron exit from the lithium photocathode
is equal to =2.4 eV [1]. Ionization energy of this electron is equal to =5.392 eV, and its binding energy with the nucleus
corresponding to the first energy level is equal to =14.05 eV
[4]. If we take it into account and use the mathematical model of the law of formation of
the atom and ion spectra (2), well get a theoretical spectrum of this electron (theor.), which
coincides completely with the experimental spectrum (exp.) (Table
1). Formula (5) gives an opportunity to calculate binding energies of this electron with the atomic nucleus (according to Einstein, the exit work), which
correspond to all () energy levels of this
electron [4].
Table 1. Spectrum of the
first electron of the lithium atom
Volumes |
n |
2 |
3 |
4 |
5 |
6 |
(exper) |
eV |
- |
3.83 |
4.52 |
4.84 |
5.01 |
(theor.) |
eV |
1.88 |
3.83 |
4.51 |
4.83 |
5.00 |
(theor.) |
eV |
3.51 |
1.56 |
0.88 |
0.56 |
0.39 |
It is known that the like atoms are
united in a molecule with the covalent bond, and binding energies between valence
electrons correspond to fractional quantum numbers [4]. It allows us to determine what is a
photoelectron emission source: atoms or molecules of the photocathode material. If we
substitute =2.4 eV and =14.05 eV in the formula
(5), well find =2.4. As value is a fractional
number, it means that the lithium molecules, not atoms are the source of the
photoelectrons (Table 1) [4].
For a photoelectron of the sodium
photocathode, we have: =5.139 eV, =13.086 eV and =2.1 eV [1], [4]. If we
use the mathematical model of the law of formation of the atom and ion spectra (2),
well get a sodium photoelectron spectrum (Table 2) [4].
Table 2. Spectrum of the 1st
electron of the sodium atom
Valumes |
n |
2 |
3 |
4 |
5 |
6 |
(exper) |
eV |
- |
3.68 |
4.31 |
4.62 |
4.78 |
(theor.) |
eV |
- |
3.68 |
4.32 |
4.62 |
4.77 |
(theor.) |
eV |
3.27 |
1.45 |
0.82 |
0.52 |
0.36 |
Value determined with the help of the formula (5) is
equal to =2.5. It appears from this that the sodium molecules, not
atoms are the source of the photoelectrons of the sodium photocathode.
The mathematical model of the law of formation of the atom and
ion spectra (2) shows that it has no orbital component of electron energy. It appears from
this that the electron has no orbital motion in the atom. The molecules are formed by
means of a combination of the unlike magnetic poles of their valence atomic electrons,
which are connected with the nuclear protons by means of the magnetic poles as well [4],
[8].
The analysis of the law of formation of
the atom and ion spectra (2) as well as the spectrum calculation results (Table 1 and 2)
show that binding energy of the electron with the atomic nucleus and,
consequently, binding energy of valence electrons of two atoms with each other is changed
step by step (5). It appears from this that kinetic energy of the photoelectrons and value of
retarding potential (Fig. 1, b) should be
changed step by step as well. The photoelectrons can absorb only the photons, which
correspond to their binding energies in the molecules of the given substance. The greater
binding energy between the electrons in the molecules, the greater photon energy is
required for the break of this bond and the greater kinetic energy the photoelectrons
being released will acquire, and the greater potential will be required for their
retardation on the way to the collector. Let us pay attention to the fact that the given
logical chain originates from the mathematical model of the law of formation of the atom
and ion spectra (2) and is present in Einsteins equation implicitly (1).
Current is present in the circuit due to
the fact that the photoelectrons emitted by the photocathode material molecules are
substituted by free electrons. They should emit the photons, which energy is equal to
binding energy of the electrons in the molecules, but light striking the photocathode does
not allow us to see this emission.
CONCLUSION
Mathematical Einsteins equation
describing experimental regularities of photoeffect has deeper physical sense. When the
components of this equation are interpreted correctly, it becomes the mathematical model
of the law of formation of the atom and ion spectra discovered by us in 1993 and published
in the papers [9], [10], [11], [12], [4].
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