Enhanced Electrochemical Water Splitting with Chiral Molecule-Coated Fe3O4 Nanoparticles

被引:140
作者
Zhang, Wenyan [1 ]
Banerjee-Ghosh, Koyel [1 ]
Tassinari, Francesco [1 ]
Naaman, Ron [1 ]
机构
[1] Weizmann Inst Sci, Dept Chem & Biol Phys, IL-76100 Rehovot, Israel
来源
ACS ENERGY LETTERS | 2018年 / 3卷 / 10期
基金
欧洲研究理事会; 中国国家自然科学基金;
关键词
PHOTOELECTROCHEMICAL CELLS; SPIN SELECTIVITY; ELECTRONS SPIN; QUANTUM DOTS; TRANSPORT;
D O I
10.1021/acsenergylett.8b01454
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
Photoelectrochemical (PEC) water splitting is a promising approach for generating hydrogen from water. In order to enhance PEC water splitting efficiency, it is essential to inhibit the production of the hydrogen peroxide byproduct and to reduce the overpotential required by an inexpensive catalyst and with high current density. In the past, it was shown that coating TiO2 electrodes by chiral molecules or chiral films enhances the hydrogen production and reduces the production of H2O2 byproduct. This was explained to be a result of the chiral-induced spin selectivity (CISS) effect that induces spin correlation between the electrons transferred to the anode. However, typically the current observed in those studies was in the range of 1-100 mu A/cm(2). Here we report currents in the range of 10 mA/cm(2) obtained by adsorbing chiral molecules on a well-established Fe3O4 nanoparticle (NP) catalyst deposited on the anode. The results indicate a new strategy for designing low-cost earth-abundant catalysts where the advantages of the CISS effect are combined with the large effective area provided by the NPs to promote PEC water splitting with high current density.
引用
收藏
页码:2308 / 2313
页数:11
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