Two-step coupled photoelectrochemical chlorination and oxygenation of C(sp<sup>3</sup>)-H bonds mediated by chlorine radicals over a modified BiVO<sub>4</sub> photoanode.
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ABSTRACT: Photoelectrochemical (PEC) cells are emerging tools for fine chemical synthesis, but often suffer from low solar-to-product conversion efficiency, especially in energy-demanding reactant activation. Herein, we report chlorination and oxygenation of energy-demanding C(sp3)-H bonds using a two-step coupled PEC cell, avoiding the direct generation of high-energy chlorine radicals (Cl˙). The photoanode consists of a BiVO4 semiconductor modified with TiO2 and a CoNi2O x chlorine evolution reaction (CER) catalyst. Under 1 sun illumination, the BiVO4/TiO2/CoNi2O x photoanode showed a photocurrent density of 2.9 mA cm-2 for CER at 0.8 V vs. the reversible hydrogen elec
SUBMITTER: Yang W
PROVIDER: S-EPMC12452966 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature
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