Heterogeneous junction engineering on core-shell nanocatalysts boosts the dye-sensitized solar cell

被引:15
|
作者
Wu, Chiun-Yi [1 ]
Liu, Yu-Ting [2 ]
Huang, Po-Chun [1 ]
Luo, Tzy-Jiun Mark [3 ]
Lee, Chih-Hao [1 ,4 ]
Yang, Yaw-Wen [4 ]
Wen, Ten-Chin [5 ]
Chen, Tsan-Yao [1 ]
Lin, Tsang-Lang [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Engn & Syst Sci, Hsinchu 30013, Taiwan
[2] Tunghai Univ, Dept Environm Sci & Engn, Taichung 40704, Taiwan
[3] N Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[4] Natl Synchrotron Radiat Res Ctr, Hsinchu, Taiwan
[5] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 70101, Taiwan
关键词
SMALL-ANGLE SCATTERING; METHANOL ELECTROOXIDATION; CARBON-MONOXIDE; FUEL-CELLS; PLATINUM; NANOPARTICLES; ELECTROCATALYSTS; SPECTROSCOPY; ELECTRODES; INTERFACE;
D O I
10.1039/c3nr02107f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we successfully manipulate the heterogeneous junction at Co3O4-Pt core-shell cathodic nanocatalysts (C/P CNCs) by controlling the core/shell ratios. Our results indicate the cobalt core atoms would inject their valence charge to the surface Pt atoms due to the presence of extensive lattice strain in the shell region. This charge injection accelerates the redox kinetics at the catalysts surface. Consequently, compared with that using Pt nanoparticle cathode, the C/P CNCs at an optimal Pt/Co atomic ratio of 1, improves the current density and the photovoltaic efficiency of dye-sensitized soar cell (DSSC) by similar to 36.3% and similar to 22.9%, respectively. By combining structure and electrochemical analysis, we systematically elucidate the effects of Pt/Co (shell/core) ratios, the interplay of Co atoms on the shell structures, and the redox activity of C/P CNCs on the DSSC performance. Hereby, this study provide mechanistic insights in developing electrocatalysts for DSSC with programmable performance and reduced Pt utilization.
引用
收藏
页码:9181 / 9192
页数:12
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