Elucidating the Conductivity-Type Transition Mechanism of p-Type Cu2O Films from Electrodeposition

被引:63
作者
Nian, Jun-Nan [1 ]
Tsai, Chien-Cheng [1 ]
Lin, Pao-Chung [1 ]
Teng, Hsisheng [1 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 70101, Taiwan
关键词
CUPROUS-OXIDE; EPITAXIAL ELECTRODEPOSITION; ELECTROCHEMICAL DEPOSITION; COPPER(I) OXIDE; N-TYPE; H-2; EVOLUTION; GROWTH; SEMICONDUCTOR; SRTIO3(100); CATALYSTS;
D O I
10.1149/1.3125800
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Narrow bandgap Cu2O films of p- and n-type conductivities are electrodeposited on conducting glass substrates from aqueous Na2SO4 solutions. These Cu2O films exhibit photoelectrochemical responses under visible light illumination. The p- and n-type films have different preferred out-of-plane orientations of [111] and [100], respectively. X-ray absorption fine structure spectroscopic analysis shows that the n-type Cu2O contains a higher degree of lattice disorder. Ultraviolet photoelectron spectroscopy along with the Mott-Schottky electrochemical impedance analysis determines the energy-level diagrams of both the p- and n-type films. On the basis of the structural features obtained, this paper finds that strong Cu2+ absorption on the unstable surface states resulting from the Cu vacancies of Cu2O can lead to the formation of an inversion layer and thus conductivity transition from p to n type. As a consequence of this p-n transition mechanism, Cu2O films containing nanocavities for strong Cu2+ absorption exhibit an n-type conductivity, while intact Cu2O films are p type. A conductivity-type diagram is constructed to show that a subtle change in the deposition parameters can tune the crystal orientation and conductivity type of Cu2O films. (C) 2009 The Electrochemical Society. [DOI: 10.1149/1.3125800] All rights reserved.
引用
收藏
页码:H567 / H573
页数:7
相关论文
共 48 条
[1]  
[Anonymous], CHEMIJA VILNIUS
[2]  
[Anonymous], 1995, PHYSICA B
[3]   Size-dependent conductivity-type inversion in Cu2O nanoparticles -: art. no. 165419 [J].
Balamurugan, B ;
Aruna, I ;
Mehta, BR ;
Shivaprasad, SM .
PHYSICAL REVIEW B, 2004, 69 (16) :165419-1
[4]   Structural investigation of combustion synthesized Cu/CeO2 catalysts by EXAFS and other physical techniques:: Formation of a Ce1-xCuxO2-δ solid solution [J].
Bera, P ;
Priolkar, KR ;
Sarode, PR ;
Hegde, MS ;
Emura, S ;
Kumashiro, R ;
Lalla, NP .
CHEMISTRY OF MATERIALS, 2002, 14 (08) :3591-3601
[5]   ELECTRIC CONDUCTIVITY AND CATALYTIC ACTIVITY OF SEMICONDUCTING OXIDE CATALYSTS [J].
BIELANSKI, A ;
DEREN, J ;
HABER, J .
NATURE, 1957, 179 (4561) :668-679
[6]   Epitaxial electrodeposition of copper(I) oxide on single-crystal gold(100) [J].
Bohannan, EW ;
Shumsky, MG ;
Switzer, JA .
CHEMISTRY OF MATERIALS, 1999, 11 (09) :2289-+
[7]   Synthesis and properties of Cu2O quantum particles [J].
Borgohain, K ;
Murase, N ;
Mahamuni, S .
JOURNAL OF APPLIED PHYSICS, 2002, 92 (03) :1292-1297
[8]   Quantum size effects in CuO nanoparticles [J].
Borgohain, K ;
Singh, JB ;
Rao, MVR ;
Shripathi, T ;
Mahamuni, S .
PHYSICAL REVIEW B, 2000, 61 (16) :11093-11096
[9]   R and C impedance components equivalent to the charge distribution within Si-substrate depletion layer [J].
Chemla, M ;
Bertagna, V ;
Erre, R ;
Rouelle, F ;
Petitdidier, S ;
Levy, D .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (01) :G7-G11
[10]   Cu2O:: Electrodeposition and characterization [J].
de Jongh, PE ;
Vanmaekelbergh, D ;
Kelly, JJ .
CHEMISTRY OF MATERIALS, 1999, 11 (12) :3512-3517