Competitive Hole Transfer from CdSe Quantum Dots to Thiol Ligands in CdSe-Cobaloxime Sensitized NiO Films Used as Photocathodes for H2 Evolution

被引:33
作者
Abdellah, Mohamed [1 ,2 ]
Zhang, Shihuai [3 ]
Wang, Mei [3 ]
Hammarstrom, Leif [1 ]
机构
[1] Uppsala Univ, Dept Chem, Angstrom Lab, Box 523, S-75120 Uppsala, Sweden
[2] South Valley Univ, Qena Fac Sci, Dept Chem, Qena 83523, Egypt
[3] Dalian Univ Technol, DUT KTH Joint Educ & Res Ctr Mol Devices, State Key Lab Fine Chem, Dalian 116024, Peoples R China
基金
瑞典研究理事会; 中国国家自然科学基金;
关键词
HYDROGEN-PRODUCTION; ALKALI POLYSULFIDES; ULTRAFAST DYNAMICS; CHARGE SEPARATION; ELECTRON-TRANSFER; INJECTION; ABSORPTION; SYSTEM; STATE; BLUE;
D O I
10.1021/acsenergylett.7b00730
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
Quantum dot (QD) sensitized NiO photocathodes rely on efficient photoinduced hole injection into the NiO valence band. A system of a mesoporous NiO film co-sensitized with CdSe QDs and a molecular proton reduction catalyst was studied. While successful electron transfer from the excited QDs to the catalyst is observed, most of the photogenerated holes are instead quenched very rapidly (ps) by hole trapping at the surface thiols of the capping agent used as linker molecules. We confirmed our conclusion by first using a thiol free capping agent and second varying the thiol concentration on the QD's surface. The later resulted in faster hole trapping as the thiol concentration increased. We suggest that this hole trapping by the linker limits the H-2 yield for this photocathode in a device.
引用
收藏
页码:2576 / 2580
页数:5
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