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Photocorrosion anodic decomposition

Fig. 15. Diagram illustrating the thermodynamic stability of a semiconductor against corrosion and photocorrosion (a) semiconductor is absolutely stable, (b) stable against cathodic decomposition, (c) stable against anodic decomposition, and (d) unstable. [From Gerischer (1977a).]... Fig. 15. Diagram illustrating the thermodynamic stability of a semiconductor against corrosion and photocorrosion (a) semiconductor is absolutely stable, (b) stable against cathodic decomposition, (c) stable against anodic decomposition, and (d) unstable. [From Gerischer (1977a).]...
Consider now the processes caused by the formation of quasilevels. As was noted above, the shift of Fn relative to F is very small for majority carriers (electrons) and can usually be neglected precisely, this was done in constructing Fig. 16b. But for minority carriers (holes) the shift of Fp can be very large. The shifts of both Fnx F and Fp increase with the growing intensity of semiconductor illumination, so that for a certain illumination intensity Fp may reach the level of the electrochemical potential of anodic decomposition Fdec, p, and Fn—the level of a certain cathodic reaction (for example, reduction of water with hydrogen evolution FHljH20). These reactions start to proceed simultaneously, and their joint action constitutes the process of photocorrosion. [Pg.289]

Photocorrosion occurs when the photogenerated holes do not oxidize water, but the semiconductor itself. The general form of this anodic decomposition reaction can be written as... [Pg.51]

Photocorrosion can be prevented by adding a redox couple to the electrolyte whose potential is more favourable than the decomposition potential such that the redox reaction occurs preferentially. When n-CdS is used as photoanode in aqueous electrolytes, the electrode is photocorroded since the reaction, CdS -1- 2h - S -1- Cd, occurs readily. By adding NaOH and sodium polysuphide to the electrolyte (Ellis et al, 1976), photocorrosion is prevented. The /S redox couple preferentially scavenges the photoholes. At the anode, sulphide is oxidized to polysulphide (free sulphur) and free sulphur is reduced back at the dark cathode. Similarly n-Si anodes have been stabilized by using a nonaqueous electrolyte containing a ferricinium/ferrocene redox couple (Legg et al, 1977 Chao et al, 1983). Unfortunately, a similar stabilization technique cannot be applied to photoelectrolysis cells. Some examples of electrode... [Pg.420]

For a certain illumination intensity, the hole quasilevel Fp at the semiconductor surface can reach the level of an anodic reaction (reaction of semiconductor decomposition in Fig. 9). In turn, the electron quasilevel F can reach, due to a shift of the Fermi level, the level of a cathodic reaction (reaction of hydrogen evolution from water in Fig. 9). Thus, both these reactions proceed simultaneously, which leads eventually to photocorrosion. Hence, nonequilibrium electrons and holes generated in a corroding semiconductor under its illumination are consumed in this case to accelerate the corresponding partial reactions. [Pg.221]

Semiconductor-Liquid Junction From Fundamentals to Solar Fuel Generating Structures, Fig. 9 Stability assessment against photocorrosion by relative alignment of quasi-Fermi levels and anodic and cathodic decomposition levels (see text) left p-semicon-ductor note that the decomposition level is located above... [Pg.1904]


See other pages where Photocorrosion anodic decomposition is mentioned: [Pg.241]    [Pg.52]    [Pg.211]    [Pg.290]    [Pg.230]    [Pg.135]    [Pg.73]   
See also in sourсe #XX -- [ Pg.283 , Pg.286 , Pg.288 ]




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