An efficient strategy for photocatalytic hydrogen peroxide production over oxygen-enriched graphitic carbon nitride with sodium phosphate

光催化 石墨氮化碳 催化作用 化学 过氧化氢 氧气 X射线光电子能谱 吸附 傅里叶变换红外光谱 氮气 无机化学 制氢 碳纤维 氮化碳 核化学 光化学 材料科学 化学工程 有机化学 复合材料 工程类 复合数
作者
Yu Zhang,Ling Zhang,Di Zeng,Wenjing Wang,Wenjing Wang,Juxue Wang,Weimin Wang,Weimin Wang,Wenzhong Wang,Wenzhong Wang
出处
期刊:Chinese Journal of Catalysis [Elsevier BV]
卷期号:43 (10): 2690-2698 被引量:30
标识
DOI:10.1016/s1872-2067(22)64114-7
摘要

Photocatalytic hydrogen peroxide (H2O2) production is a promising strategy to replace the traditional production processes; however, the inefficient H2O2 productivity limits its application. In this study, oxygen-rich g-C3N4 with abundant nitrogen vacancies (OCN) was synthesized for photocatalytic H2O2 production. X-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy indicated that oxygen-containing functional groups (–COOH and C–O–C) were obtained. Electron paramagnetic resonance confirmed the successful introduction of nitrogen vacancies. OCN exhibited efficient photocatalytic H2O2 production performance of 1965 µmol L−1 h−1 in air under visible-light irradiation. The high H2O2 production was attributed to the enhanced adsorption of oxygen, enlarged specific surface area, and promoted carrier separation. An increased H2O2 production rate (5781 µmol L−1 h−1) was achieved in a Na3PO4 solution. The improved performance was attributed to the changed reactive oxygen species. Specifically, the adsorbed PO43− on the surface of the OCN promoted the transfer of holes to the catalyst surface. •O2− obtained by O2 reduction reacted with adjacent holes to generate 1O2, which could efficiently generate H2O2 with isopropanol. Additionally, PO43−, as a stabilizer, inhibited the decomposition of H2O2.
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