An Interpretation of the Selective Photo-Electric Effect from Two-Component Cathodes

Abstract

Evidence is produced to support the view that photoelectrically selective, two component cathodic surfaces are crystalline in nature. Then, assuming that Fowler's equation for the energy of electrons selectively transmitted through a single potential valley [$W=(\frac{{n}^{2}{h}^{2}}{8m{d}^{2}})$] is equally valid for the energy of electrons selectively transmitted through the periodic sequence of valleys characteristic of the potential field within a crystal, and that all of the energy of photoelectrons is acquired from the incident light quanta, the wave-lengths of light to which such a surface should respond selectively can be computed. Such computations have been made with $d$ equal to the internuclear distance between electro-positive ions in the lattice structure of alkali metal hydride, oxide and sulphide crystals. The hydride crystals belong to the sodium chloride type and the oxide and sulphide crystals are supposedly of the calcium-fluoride type. The correlation between these computed values and the positions of the observed selective maxima is exceptionally good. Moreover, the fact that the alkali metal hydrides exhibit but one selective maximum and the oxides two or three maxima is in keeping with the geometry of their respective crystalline types.