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The oxygen dimer in Si: Its relationship to the light-induced degradation of Si solar cells?
Author(s) -
Л.И. Мурин,
Е. А. Толкачева,
В. П. Маркевич,
А. R. Peaker,
B. Hamilton,
Edouard V. Monakhov,
B. G. Svensson,
J. L. Lindström,
P. Santos,
J. Coutinho,
Alexandra Carvalho
Publication year - 2011
Publication title -
applied physics letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 442
eISSN - 1077-3118
pISSN - 0003-6951
DOI - 10.1063/1.3584138
Subject(s) - dimer , excited state , silicon , photochemistry , oxygen , absorption (acoustics) , chemical physics , degradation (telecommunications) , solar cell , charge (physics) , materials science , chemistry , molecular physics , atomic physics , optoelectronics , physics , organic chemistry , telecommunications , quantum mechanics , computer science , composite material
It is widely believed that the light induced degradation of crystalline silicon solar cells is due to the formation of a BsO2i recombination center created by the optically excited migration of the oxygen dimer (charge-state-driven motion). In this letter the concentration dependence of the neutral state of O2i on [Oi] in p- and n-type Cz–Si has been determined using infrared absorption. A systematic search for the absorption signature of the dimer in the doubly positively charged state has been unsuccessful. These data strongly suggest that charge-state-driven motion (Bourgoin–Corbett mechanism) of the oxygen dimer cannot occur in typical solar silicon and hence bring into question the accepted degradation mechanism.

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