Flat band potential
 | This article may be too technical for most readers to understand. (May 2021) |
In semiconductor physics, the flat band potential of a semiconductor defines the potential at which there is no depletion layer at the junction between a semiconductor and an electrolyte[1] or p-n-junction. This is a consequence of the condition that the redox Fermi level of the electrolyte must be equal to the Fermi level of the semiconductor [1] and therefore preventing any band bending of the conduction and valence band. An application of the flat band potential can be found in the determining the width of the space charge region in a semiconductor-electrolyte junction.[2] Furthermore, it is used in the Mott-Schottky equation to determine the capacitance of the semiconductor-electrolyte junction [3][4][5] and plays a role in the photocurrent of a photoelectrochemical cell.[2][5] The value of the flat band potential depends on many factors, such as the material, pH and crystal structure of the material[3][6][7]
Background semiconductor physics
[edit]In semiconductors, valence electrons are located in energy bands. According to band theory,[8][9] the electrons are either located in the valence band (lower energy) or the conduction band (higher energy), which are separated by an energy gap. In general, electrons will occupy different energy levels following the Fermi-Dirac distribution; for energy levels higher than the Fermi energy Ef, the occupation will be minimal. Electrons in lower levels can be excited into the higher levels through thermal or photoelectric excitations, leaving a positively-charged hole in the band they left.[9][8] Due to conservation of net charge, the concentration of electrons (n) and of protons or holes (p) in a (pure) semiconductor must always be equal. Semiconductors can be doped to increase these concentrations: n-doping increases the concentration of electrons while p-doping increases the concentration of holes. This also affects the Fermi energy of the electrons: n-doped means a higher Fermi energy, while p-doped means a lower energy. At the interface between a n-doped and p-doped region in a semiconductor, band bending will occur.[9][8] Due to the different charge distributions in the regions, an electric field will be induced, creating a so-called depletion region at the interface. Similar interfaces also appear at junctions between (doped) semiconductors and other materials, such as metals/electrolytes. A way to counteract this band bending is by applying a potential to the system. This potential would have to be the flat band potential and is defined to be the applied potential at which the conduction and valence bands become flat[9]
References
[edit]- ^ a b Sixto Giménez and Juan Bisquert. Photoelectrochemical Solar Fuel Production. Springer, Switzerland, 2016.
- ^ a b M Sharon. An Introduction to the Physics and Electrochemistry of Semiconductors. John Wiley & sons, inc and Scrivener Publishing LLC, New Jersey and Beverly, 2016.
- ^ a b K. Gelderman, L. Lee, and S. W. Donne. Flat-band potential of a semiconductor: Using the mott–schottky equation. Journal of Chemical Education, 84(4):685, 2007.
- ^ W. John Albery, Gerald J. O’Shea, and Alec L. Smith. Interpretation and use of mott–schottky plots at the semiconductor/electrolyte interface. J. Chem. Soc., Faraday Trans., 92:4083–4085, 1996.
- ^ a b Anna Hankin, Franky E. Bedoya-Lora, John C. Alexander, Anna Regoutz, and Geoff H. Kelsall. Flat band potential determination: avoiding the pitfalls. J. Mater. Chem. A, 7:26162–26176, 2019.
- ^ M. Radecka, M. Rekas, A. Trenczek-Zajac, and K. Zakrzewska. Importance of the band gap energy and flat band potential for application of modified tio2 photoanodes in water photolysis. Journal of Power Sources, 181(1):46 – 55, 2008. SPECIAL SECTION Selected papers from the 1st POLISH FORUM ON FUEL CELLS AND HYDROGEN.
- ^ E. C. Dutoit, F. Cardon, and W. P. Gomes. Electrochemical properties of the semiconducting tio2 (rutile) single crystal electrode. Berichte der Bunsengesellschaft f¨ur physikalische Chemie, 80(6):475–481, 1976.
- ^ a b c Steven H. Simon. The Oxford Solid State Basics. Oxford, Oxford, 2013.
- ^ a b c d Giménez, Sixto; Bisquert, Juan (29 April 2016). Photoelectrochemical solar fuel production : from basic principles to advanced devices. Switzerland. ISBN 978-3-319-29641-8. OCLC 948632302.
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