过电位
阳极
电化学
纳米颗粒
分子
电流密度
材料科学
过氧化氢
分解水
纳米技术
化学工程
氢
制氢
化学
无机化学
物理化学
电极
有机化学
催化作用
物理
光催化
量子力学
工程类
作者
Wenyan Zhang,Koyel Banerjee-Ghosh,Francesco Tassinari,Ron Naaman
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-09-04
卷期号:3 (10): 2308-2313
被引量:127
标识
DOI:10.1021/acsenergylett.8b01454
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 μA/cm2. Here we report currents in the range of 10 mA/cm2 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI