Highly selective photocatalytic production of H2O2 on sulfur and nitrogen co-doped graphene quantum dots tuned TiO2

光催化 石墨烯 光化学 电子转移 石墨烯量子点 化学 量子产额 量子点 制氢 过氧化氢 材料科学 纳米技术 催化作用 有机化学 物理 荧光 光学
作者
Longhui Zheng,Hanrui Su,Jingzhen Zhang,Laxman S. Walekar,Hamed Vafaei Molamahmood,B. Zhou,Mingce Long,Yun Hang Hu
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:239: 475-484 被引量:234
标识
DOI:10.1016/j.apcatb.2018.08.031
摘要

Photocatalytic production of hydrogen peroxide (H2O2) using water and molecular oxygen as the sole material source is a promising and sustainable solar fuel approach. Herein, we developed an efficient photocatalyst (SN-GQD/TiO2) for H2O2 syntheses by tuning TiO2 with sulfur and nitrogen co-doped graphene quantum dots (SN-GQDs). The high luminescent SN-GQDs homogeneously dispersed on TiO2 surface, which induces the extended visible light absorption and enhanced electron migration. The SN-GQD/TiO2 exhibited 3.2 times H2O2 yield (451 μmol L−1) as that of bare TiO2 under simulated sunlight irradiation, which was also significantly higher than that over GQD/TiO2 and N-GQD/TiO2. Kinetic evaluations suggested that the formation of H2O2 on SN-GQD/TiO2 was dramatically accelerated by 2.4 times compared with that on TiO2, while the decomposition of H2O2 was moderately suppressed (only 25% reduction). The increased H2O2 formation on SN-GQD/TiO2 was attributed to the boosted two-electron reduction of oxygen, which was confirmed by the electron transfer numbers (n = 2.2) obtained from Koutecky-Levuch plots, the less sensitivity of H2O2 production to pH, and the insignificant signals for DMPO–O2− in ESR measurements. According to theoretical calculations and free energy diagrams of the ORR pathway, a mechanism of proton-coupled electron transfer (PCET) to produce H2O2 was proposed to understand the highly selective two-electron H2O2 production on SN-GQD/TiO2. This study brings an insight to modulate highly selective two-electron photocatalytic reduction of oxygen by introduction of dual doped GQDs that can provide active sites for *OOH formation and proton relays.
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