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Fermi‐level pinning and effect of deposition bath pH on the flat‐band potential of electrodeposited n‐Cu 2 O in an aqueous electrolyte
Author(s) -
Kafi F. S. B.,
Jayathileka K. M. D. C.,
Wijesundera R. P.,
Siripala W.
Publication year - 2016
Publication title -
physica status solidi (b)
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.51
H-Index - 109
eISSN - 1521-3951
pISSN - 0370-1972
DOI - 10.1002/pssb.201600288
Subject(s) - electrolyte , photocurrent , aqueous solution , volta potential , fermi level , analytical chemistry (journal) , band gap , deposition (geology) , surface states , materials science , schottky barrier , chemical bath deposition , chemistry , nanotechnology , electrode , optoelectronics , kelvin probe force microscope , physics , surface (topology) , electron , atomic force microscopy , mathematics , biology , paleontology , geometry , chromatography , quantum mechanics , diode , sediment
Capacitance–voltage ( C–V ) and modulated light‐induced current–voltage measurements were employed to investigate the Cu 2 O/electrolyte junction of electrodeposited n‐Cu 2 O thin films. The Mott–Schottky plots resulting from the C–V measurements revealed that the extrapolated flat‐band potential of n‐Cu 2 O films was strongly influenced by the pH of the bath where the films were grown. The flat‐band potential change was 300 mV for a pH difference of 0.8 and showed that the surface chemistry at an n‐Cu 2 O/aqueous electrolyte interface was strongly affected by the pH of the film deposition bath. In addition, current–potential measurements revealed that at the measured flat‐band potential the photocurrent did not vanish for n‐Cu 2 O films and the Fermi level at the interface was pinned due to the presence of electrically active surface states. Information on the presence of electrically active surface states and the shift in flat‐band potential will be very useful for applications of n‐Cu 2 O films in various devices.