A Cobalt@Cucurbit[5]uril Complex as a Highly Efficient Supramolecular Catalyst for Electrochemical and Photoelectrochemical Water Splitting

被引:75
作者
Li, Fusheng [1 ]
Yang, Hao [2 ]
Zhuo, Qiming [1 ]
Zhou, Dinghua [1 ]
Wu, Xiujuan [1 ]
Zhang, PeiLi [1 ]
Yao, Zhaoyang [2 ]
Sun, Licheng [1 ,2 ,3 ]
机构
[1] Dalian Univ Technol, DUT KTH Joint Educ & Res Ctr Mol Devices, Inst Artificial Photosynth, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] KTH Royal Inst Technol, Sch Engn Sci Chem Biotechnol & Hlth, Dept Chem, S-10044 Stockholm, Sweden
[3] Westlake Univ, Ctr Artificial Photosynth Solar Fuels, Sch Sci, Hangzhou 310024, Peoples R China
基金
瑞典研究理事会; 中国国家自然科学基金;
关键词
electrocatalysis; host– guest complexes; PEC cells; supramolecular catalysts; water splitting; BIVO4; PHOTOANODES; REACTION-KINETICS; SURFACE; OXIDATION; PERFORMANCE; LAYER;
D O I
10.1002/anie.202011069
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A host-guest complex self-assembled through Co2+ and cucurbit[5]uril (Co@CB[5]) is used as a supramolecular catalyst on the surface of metal oxides including porous indium tin oxide (ITO) and porous BiVO4 for efficient electrochemical and photoelectrochemical water oxidation. When immobilized on ITO, Co@CB[5] exhibited a turnover frequency (TOF) of 9.9 s(-1) at overpotential eta=550 mV in a pH 9.2 borate buffer. Meanwhile, when Co@CB[5] complex was immobilized onto the surface of BiVO4 semiconductor, the assembled Co@CB[5]/BiVO4 photoanode exhibited a low onset potential of 0.15 V (vs. RHE) and a high photocurrent of 4.8 mA cm(-2) at 1.23 V (vs. RHE) under 100 mW cm(-2) (AM 1.5) light illumination. Kinetic studies confirmed that Co@CB[5] acts as a supramolecular water oxidation catalyst, and can effectively accelerate interfacial charge transfer between BiVO4 and electrolyte. Surface charge recombination of BiVO4 can be also significantly suppressed by Co@CB[5].
引用
收藏
页码:1976 / 1985
页数:10
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