双功能
分解水
异质结
阳极
材料科学
阴极
过渡金属
纳米技术
化学物理
化学工程
化学
光电子学
物理化学
电极
催化作用
光催化
生物化学
工程类
作者
Yali Liu,Xiaohu Luo,Chengliang Zhou,Shuo Du,Deshuai Zhen,Bo Chen,Ji Li,Qian Wu,Yorhyikazcu Iru,Dongchu Chen
标识
DOI:10.1016/j.apcatb.2019.118197
摘要
Herein, we report a rational design of one-dimension (1D) porous hybrid heterostructures with the active HER (Mo2C) and OER (Co4S3) embedded N and S co-doped carbon (Co4S3/Mo2 C-N SC) for the effective overall water splitting. Spectroscopic characterizations reveals that modulated electronic state behaviors are generated by the strong chemical couplings at the nanointerface which triggers the charge from Co2+ to Mo4+/Mo6+ through the interfacial Mo-S-Co bond, resulting in producing the considerable amounts of the active sites (i.e., Co3+, Mo2+, and Mo3+) for the HER and OER in the hybrid heterostructures. Interestingly, Co4S3/Mo2 C-N SC shows pronounced synergistic effects in electrocatalytic activity for the HER and OER. When Co4S3/Mo2 C-N SC is used as both anode and cathode for overall water splitting, a low cell voltage of 1.62 eV is generated at 10 mA cm−2. The interesting work highlights the significance of optimization electronic structure based on transition metal-based bifunctional electrocatalysts for the HER and OER.
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