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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 η=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].
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Li et al. (2020) studied this question.
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