Characterization and Polymerization of Thienylphenyl and Selenylphenyl Amines and Their Interaction with CdSe Quantum Dots

被引:0
作者
Lana-Villarreal, Teresa [1 ,2 ]
Font-Sanchis, Enrique [3 ]
Sastre-Santos, Angela [3 ]
Fernandez-Lazaro, Fernando [3 ]
Gomez, Roberto [1 ,2 ]
机构
[1] Univ Alacant, Inst Univ Electroquim, Alacant 03080, Spain
[2] Univ Alacant, Dept Quim Fis, Alacant 03080, Spain
[3] Univ Miguel Hernandez Elche, Inst Bioingn, Div Quim Organ, Elche 03202, Spain
关键词
amines; charge transfer; electropolymerization; quantum dots; solar cells; HETEROJUNCTION SOLAR-CELLS; OXIDATIVE CROSS-LINKING; MOLECULAR MATERIALS; NANOCRYSTALS; PHOTOLUMINESCENCE; PERFORMANCE; THIOPHENE; ELECTRODE; DEVICES; SYSTEMS;
D O I
10.1002/cphc.201001069
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hybrid quantum-dot-sensitized solar cells show promising novel optoelectronic properties. An adequate design of such cells requires a deep understanding of the characteristics of each component, including their interactions. In this context, the electrochemical properties of two different hole-transporting materials (HTMs) and their chemical interactions with trioc-tylphosphine- capped CdSe quantum dots are investigated to evaluate their potential use in hybrid quantum-dot-sensitized solar cells. Tris[4-(thien-2-yl)phenyl]amine (TTPA) and tris[4(selen-2-yl)phenyl] amine (TSePA) are studied in the solid state as thin films deposited on a conducting substrate. Spectroelectrochemical studies evidence both solid-state electropolymerization and doping. Upon addition of TSePA or partially polymerized TTPA to a colloidal solution of trioctylphosphine-capped CdSe quantum dots, the steady-state photoluminescence is quenched. This suggests that the quantum dots and the HTM strongly interact, probably through an excited-state charge-transfer mechanism. The combination of all these pieces of information indicates that polymerized TTPA and TSePA are potential candidates as HTMs for hybrid quantumdot-sensitized solar cells.
引用
收藏
页码:1155 / 1164
页数:10
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