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High‐efficient photoelectrocatalytic direct ammonia oxidation reaction (AOR) conducted on semiconductor photoanodes remains a substantial challenge. Herein, we develop a strategy of simply introducing ppm levels of Cu ions (0.5–10 mg/L) into NH3 solutions to significantly improve the AOR photocurrent of bare BiVO4 photoanodes from 3.4 to 6.3 mA cm−2 at 1.23 VRHE, being close to the theoretical maximum photocurrent of BiVO4 (7.5 mA cm−2). The surface charge‐separation efficiency has reached 90 % under a low bias of 0.8 VRHE. This AOR exhibits a high Faradaic efficiency (FE) of 93.8 % with the water oxidation reaction (WOR) being greatly suppressed. N2 is the main AOR product with FEs of 71.1 % in aqueous solutions and FEs of 100 % in non‐aqueous solutions. Through mechanistic studies, we find that the formation of Cu−NH3 complexes possesses preferential adsorption on BiVO4 surfaces and efficiently competes with WOR. Meanwhile, the cooperation of BiVO4 surface effect and Cu‐induced coordination effect activates N−H bonds and accelerates the first rate‐limiting proton‐coupled electron transfer for AOR. This simple strategy is further extended to other photoanodes and electrocatalysts. [ABSTRACT FROM AUTHOR]

Herein we report the vital role of spin polarization in proton‐transfer‐mediated water oxidation over a magnetized catalyst. During the electrochemical oxygen evolution reaction (OER) over ferrimagnetic Fe3O4, the external magnetic field induced a remarkable increase in the OER current, however, this increment achieved in weakly alkaline pH (pH 9) was almost 20 times that under strongly alkaline conditions (pH 14). The results of the surface modification experiment and H/D kinetic isotope effect investigation confirm that, at weakly alkaline pH, during the nucleophilic attack of FeIV=O by molecular water, the magnetized Fe3O4 catalyst polarizes the spin states of the nucleophilic attacking intermediates. The spin‐enhanced singlet O−H cleavage and triplet O−O bonding occur synergistically, which promotes the O2 generation more significantly than the strongly alkaline case involving only spin‐enhanced O−O bonding. [ABSTRACT FROM AUTHOR]

The sluggish H2O oxidation kinetics on photoanodes severely obstructs the overall solar‐to‐energy efficiency of photoelectrochemical (PEC) cells. Herein, we find a 10 to 55‐fold increase of photocurrent by conducting ammonia oxidation reaction (AOR) on hematite (α‐Fe2O3) photoanodes under near‐neutral pH (9–11) and moderate applied potentials (1.0–1.4 VRHE) compared to H2O oxidation. By rate law analysis and operando spectroscopic studies, we confirm the non‐radical nucleophilic attack of NH3 molecules on high‐valent surface Fe−O species (e.g. FeIV=O) and Fe−N species that produces NOx− and N2, respectively, which overwhelms the nucleophilic attack of H2O on surface FeIV=O and contributes to a high Faradaic efficiency of above 80 % for AOR. This work reveals a novel non‐radical nucleophilic attack strategy, which is significantly different from the conventional indirect radical‐mediated AOR mechanism, for the rational design of high‐performance AOR photoelectrocatalysts. [ABSTRACT FROM AUTHOR]