11.4 Experimental Study of Photoelectric Effect

11-1

Experimental arrangement for study of photoelectric effect.

Figure 11-1 depicts a schematic view of the arrangement used for the experimental study of the photoelectric effect. It consists of an evacuated glass/quartz tube having a thin photosensitive plate C and another metal plate A. Monochromatic light from the source S of sufficiently short wavelength passes through the window W and falls on the photosensitive plate C (emitter). A transparent quartz window is sealed on to the glass tube, which permits ultraviolet radiation to pass through it and irradiate the photosensitive plate C. The electrons are emitted by the plate C and are collected by the plate A (collector), by the electric field created by the battery. The battery maintains the potential difference between the plates C and A, that can be varied. The polarity of the plates C and A can be reversed by a commutator. Thus, the plate A can be maintained at a desired positive or negative potential with respect to emitter C. When the collector plate A is positive with respect to the emitter plate C, the electrons are attracted to it. The emission of electrons causes flow of electric current in the circuit. The potential difference between the emitter and collector plates is measured by a voltmeter (V) whereas the resulting photo current flowing in the circuit is measured by a microammeter (µA). The photoelectric current can be increased or decreased by varying the potential of collector plate A with respect to the emitter plate C. The intensity and frequency of the incident light can be varied, as can the potential difference V between the emitter C and the collector A.

We can use the experimental arrangement of Fig. 11.1 to study the variation of photocurrent with (a) intensity of radiation, (b) frequency of incident radiation, (c) the potential difference between the plates A and C, and (d) the nature of the material of plate C. Light of different frequencies can be used by putting appropriate coloured filter or coloured glass in the path of light falling on the emitter C. The intensity of light is varied by changing the distance of the light source from the emitter.

11.4.1 Effect of intensity of light on photocurrent

The collector A is maintained at a positive potential with respect to emitter C so that electrons ejected from C are attracted towards collector A. Keeping the frequency of the incident radiation and the potential fixed, the intensity of light is varied and the resulting photoelectric current is measured each time. It is found that the photocurrent increases linearly with intensity of incident light as shown graphically in Fig. 11.2. The photocurrent is directly proportional to the number of photoelectrons emitted per second. This implies that the number of photoelectrons emitted per second is directly proportional to the intensity of incident radiation.

11-2

Variation of Photoelectric current with intensity of light.

11.4.2 Effect of potential on photoelectric current

We first keep the plate A at some positive potential with respect to the plate C and illuminate the plate C with light of fixed frequency ν and fixed intensity \(I_{1}\) . We next vary the positive potential of plate A gradually and measure the resulting photocurrent each time. It is found that the photoelectric current increases with increase in positive (accelerating) potential. At some stage, for a certain positive potential of plate A, all the emitted electrons are collected by the plate A and the photoelectric current becomes maximum or saturates. If we increase the accelerating potential of plate A further, the photocurrent does not increase. This maximum value of the photoelectric current is called saturation current. Saturation current corresponds to the case when all the photoelectrons emitted by the emitter plate C reach the collector plate A.

We now apply a negative (retarding) potential to the plate A with respect to the plate C and make it increasingly negative gradually. When the polarity is reversed, the electrons are repelled and only the sufficiently energetic electrons are able to reach the collector A. The photocurrent is found to decrease rapidly until it drops to zero at a certain sharply defined, critical value of the negative potential V 0 on the plate A. For a particular frequency of incident radiation, the minimum negative (retarding) potential V 0 given to the plate A for which the photocurrent stops or becomes zero is called the cut-off or stopping potential.

The interpretation of the observation in terms of photoelectrons is straightforward. All the photoelectrons emitted from the metal do not have the same energy. Photoelectric current is zero when the stopping potential is sufficient to repel even the most energetic photoelectrons, with the maximum kinetic energy (\(K_{max}\) ), so that

\[ K_{\max }=e V_{0} \]

11-3

Variation of photocurrent with collector plate potential for different intensity of incident radiation.

We can now repeat this experiment with incident radiation of the same frequency but of higher intensity \(I_{2}\) and \(I_{3}\) (\(I_{3}\) > \(I_{2}\) > \(I_{1}\) ). We note that the saturation currents are now found to be at higher values. This shows that more electrons are being emitted per second, proportional to the intensity of incident radiation. But the stopping potential remains the same as that for the incident radiation of intensity \(I_{1}\) , as shown graphically in Fig. 11.3. Thus, for a given frequency of the incident radiation, the stopping potential is independent of its intensity. In other words, the maximum kinetic energy of photoelectrons depends on the light source and the emitter plate material, but is independent of intensity of incident radiation.

11.4.3 Effect of frequency of incident radiation on stopping potential

11-4

Variation of photoelectric current with collector plate potential for different frequencies of incident radiation.

We now study the relation between the frequency ν of the incident radiation and the stopping potential V 0 . We suitably adjust the same intensity of light radiation at various frequencies and study the variation of photocurrent with collector plate potential. The resulting variation is shown in Fig. 11.4. We obtain different values of stopping potential but the same value of the saturation current for incident radiation of different frequencies. The energy of the emitted electrons depends on the frequency of the incident radiations. The stopping potential is more negative for higher frequencies of incident radiation. Note from Fig. 11.4 that the stopping potentials are in the order \(V_{03}\)> \(V_{02}\) > \(V_{01}\) if the frequencies are in the order \(ν_{3}\) > \(ν_{2}\) > \(ν_{1}\) . This implies that greater the frequency of incident light, greater is the maximum kinetic energy of the photoelectrons. Consequently, we need greater retarding potential to stop them completely. If we plot a graph between the frequency of incident radiation and the corresponding stopping potential for different metals we get a straight line, as shown in Fig. 11.5.

11-5

Variation of stopping potential \(V_{0}\)with frequency ν of incident radiation for a given photosensitive material.

The graph shows that

  1. the stopping potential \(V_{0}\) varies linearly with the frequency of incident radiation for a given photosensitive material.
  2. there exists a certain minimum cut-off frequency ν 0 for which the stopping potential is zero.

These observations have two implications:

  1. The maximum kinetic energy of the photoelectrons varies linearly with the frequency of incident radiation, but is independent of its intensity.
  2. For a frequency ν of incident radiation, lower than the cut-off frequency \(ν_{0}\) , no photoelectric emission is possible even if the intensity is large.
This minimum, cut-off frequency ν 0 , is called the threshold frequency. It is different for different metals.

Different photosensitive materials respond differently to light. Selenium is more sensitive than zinc or copper. The same photosensitive substance gives different response to light of different wavelengths. For example, ultraviolet light gives rise to photoelectric effect in copper while green or red light does not.

Note that in all the above experiments, it is found that, if frequency of the incident radiation exceeds the threshold frequency, the photoelectric emission starts instantaneously without any apparent time lag, even if the incident radiation is very dim. It is now known that emission starts in a time of the order of 1\(0^{–9}\) s or less.

We now summarise the experimental features and observations described in this section.

  1. For a given photosensitive material and frequency of incident radiation (above the threshold frequency), the photoelectric current is directly proportional to the intensity of incident light (Fig. 11.2)
  2. For a given photosensitive material and frequency of incident radiation, saturation current is found to be proportional to the intensity of incident radiation whereas the stopping potential is independent of its intensity (Fig. 11.3).
  3. For a given photosensitive material, there exists a certain minimum cut-off frequency of the incident radiation, called the threshold frequency, below which no emission of photoelectrons takes place, no matter how intense the incident light is. Above the threshold frequency, the stopping potential or equivalently the maximum kinetic energy of the emitted photoelectrons increases linearly with the frequency of the incident radiation, but is independent of its intensity (Fig. 11.5).
  4. The photoelectric emission is an instantaneous process without any apparent time lag (\(∼10^{–9}\) s or less), even when the incident radiation is made exceedingly dim

Next Section ->