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

A host–guest complex self‐assembled through Co(2+) 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 BiVO(4) for efficient electrochemical and photoelectrochemical water oxidation. When immobilized on...

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Detalles Bibliográficos
Autores principales: Li, Fusheng, Yang, Hao, Zhuo, Qiming, Zhou, Dinghua, Wu, Xiujuan, Zhang, PeiLi, Yao, Zhaoyang, Sun, Licheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894348/
https://www.ncbi.nlm.nih.gov/pubmed/33051952
http://dx.doi.org/10.1002/anie.202011069
Descripción
Sumario:A host–guest complex self‐assembled through Co(2+) 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 BiVO(4) 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 η=550 mV in a pH 9.2 borate buffer. Meanwhile, when Co@CB[5] complex was immobilized onto the surface of BiVO(4) semiconductor, the assembled Co@CB[5]/BiVO(4) 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 BiVO(4) and electrolyte. Surface charge recombination of BiVO(4) can be also significantly suppressed by Co@CB[5].