Efficient photocatalytic hydrogen peroxide generation coupled with selective benzylamine oxidation over defective ZrS<sub>3</sub> nanobelts.

Tian, Zhangliu; Han, Cheng; Zhao, Yao; Dai, Wenrui; Lian, Xu; Wang, Yanan; Zheng, Yue; Shi, Yi et al. · Nat Commun · 2021

basic_science · Level V

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Abstract

Photocatalytic hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) generation represents a promising approach for artificial photosynthesis. However, the sluggish half-reaction of water oxidation significantly limits the efficiency of H<sub>2</sub>O<sub>2</sub> generation. Here, a benzylamine oxidation with more favorable thermodynamics is employed as the half-reaction to couple with H<sub>2</sub>O<sub>2</sub> generation in water by using defective zirconium trisulfide (ZrS<sub>3</sub>) nanobelts as a photocatalyst. The ZrS<sub>3</sub> nanobelts with disulfide (S<sub>2</sub><sup>2-</sup>) and sulfide anion (S<sup>2-</sup>) vacancies exhibit an excellent photocatalytic performance for H<sub>2</sub>O<sub>2</sub> generation and simultaneous oxidation of benzylamine to benzonitrile with a high selectivity of >99%. More importantly, the S<sub>2</sub><sup>2-</sup> and S<sup>2-</sup> vacancies can be separately introduced into ZrS<sub>3</sub> nanobelts in a controlled manner. The S<sub>2</sub><sup>2-</sup> vacancies are further revealed to facilitate the separation of photogenerated charge carriers. The S<sup>2-</sup> vacancies can significantly improve the electron conduction, hole extraction, and kinetics of benzylamine oxidation. As a result, the use of defective ZrS<sub>3</sub> nanobelts yields a high production rate of 78.1 ± 1.5 and 32.0 ± 1.2 μmol h<sup>-1</sup> for H<sub>2</sub>O<sub>2</sub> and benzonitrile, respectively, under a simulated sunlight irradiation.