A New and stable Mo-Mo2C modified g-C3N4 photocatalyst for efficient visible light photocatalytic H2 production

光催化 石墨氮化碳 材料科学 催化作用 纳米复合材料 贵金属 金属 纳米颗粒 可见光谱 制氢 氮化物 化学工程 纳米技术 化学 冶金 有机化学 图层(电子) 工程类 光电子学
作者
Jie Dong,Ying Shi,Cunping Huang,Qiang Wu,Tao Zeng,Weifeng Yao
出处
期刊:Applied Catalysis B-environmental [Elsevier]
卷期号:243: 27-35 被引量:176
标识
DOI:10.1016/j.apcatb.2018.10.016
摘要

Design and preparation of highly efficient and stable cocatalysts are critical to the improvement of photocatalyst performance. A traditional cocatalyst consists of metal nanoparticles for the separation of photo-induced electron-hole pairs and for the reduction of protons. In this research we report a metal-semiconductor composite cocatalyst to increase light adsorption and to effectively enhance proton reduction capacity. A molybdenum rich molybdenum carbide (Mo-Mo2C) based noble-metal-free metal/semiconductor cocatalyst was loaded onto graphitic carbon nitride (g-C3N4) for highly efficient photocatalytic H2 evolution from water. The Mo-Mo2C was synthesized via a temperature-programmed reaction using (NH4)6Mo7O24·4H2O as a precursor. The cocatalyst loaded 2.0 wt.% Mo-Mo2C/g-C3N4 composite photocatalyst has demonstrated excellent photocatalytic performance. The hydrogen evolution rate for the 2.0 wt.% Mo-Mo2C/g-C3N4 nanocomposites can be as high as 219.7 μmol h−1 g−1, which is 440 times higher than that of g-C3N4 alone and 90% as high as 0.5 wt.% Pt/g-C3N4 photocatalyst (244.1 μmol h−1 g−1). Due to strong synergetic effects between Mo and Mo2C nanoparticles, this rate is 11.47 and 3.60 times higher than those for 2.0 wt.% Mo/g-C3N4 (19.1 μmol h−1 g−1) and 2.0 wt.% Mo2C/g-C3N4 (60.9 μmol h−1 g−1) photocatalysts respectively. Moreover, the 2.0 wt.% Mo-Mo2C/g-C3N4 catalyst is significantly stable for application in photocatalytic hydrogen evolution, with an apparent quantum efficiency of 8.3%—one of the highest noble-metal-free efficiencies reported in literature. All results indicate that metal/semiconductor composites can serve as highly efficient cocatalysts for photocatalytic hydrogen evolution from water reduction.
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