Holey graphitic carbon nitride (g-CN) supported bifunctional single atom electrocatalysts for highly efficient overall water splitting

被引:190
作者
Lv, Xingshuai [1 ]
Wei, Wei [1 ]
Wang, Hao [1 ]
Huang, Baibiao [1 ]
Dai, Ying [1 ]
机构
[1] Shandong Univ, Sch Phys, State Key Lab Crystal Mat, Jinan 250100, Peoples R China
基金
中国国家自然科学基金;
关键词
bifunctional electrocatalysts; single atom catalysts; overall water splitting; holey graphitic carbon nitride; RUTHENIUM-BASED CATALYST; OXYGEN REDUCTION; CO2; REDUCTION; N-2; FIXATION; EVOLUTION; GRAPHENE; EXCHANGE; DENSITY; ANODES;
D O I
10.1016/j.apcatb.2019.118521
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
Downsizing metal-based catalysts to construct single atom catalysts (SACs) is currently an emerging focus in research community of electrocatalysis, however, encountering the common aggregation of metal sites. Herein, the catalytic performance of holey g-CN supported SACs (Ti, V, Cr, Mn, Fe, Co and Ni) toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are evaluated. Co-1/g-CN and Ni-1/g-CN are identified as the most efficient bifunctional single atom catalysts for overall water splitting, capable of driving HER/OER simultaneously with overpotentials being as low as 0.15/0.61 V and 0.12/0.40 V, outperforming the commercial Pt and IrO2. Remarkably, the d band centers of TM atoms can act as an efficient descriptor for the interaction strength between intermediates and TM/g-CN, which can be tuned to further optimize the catalytic activity. This work heralds a new family of bifunctional single atom electrocatalysts for overall water splitting, elucidating a useful guideline for designing advanced SACs.
引用
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页数:7
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