CNT/g-C3 N4 photocatalysts with enhanced hydrogen evolution ability for water splitting based on a noncovalent interaction

光催化 分解水 材料科学 制氢 光电效应 石墨氮化碳 氮化碳 碳纳米管 化学工程 催化作用 量子产额 纳米技术 光化学 化学 光电子学 有机化学 光学 工程类 物理 荧光
作者
Limin Song,Xingsi Kang,Shujuan Zhang
出处
期刊:International Journal of Energy Research [Wiley]
卷期号:42 (4): 1649-1656 被引量:43
标识
DOI:10.1002/er.3960
摘要

Graphite carbon nitride (g-C3N4) as a novel photocatalyst has attracted growing attention, but its photocatalytic efficiency should be further improved. Based on the large work function and fast electron conductivity of carbon nanotubes (CNTs), here CNT/g-C3N4 photocatalysts with improved H2 evolution ability and stable water splitting ability were synthesized. The improvement was attributed to the synergistic effect between CNTs and g-C3N4. As for the mechanisms, CNTs strongly attracted photoelectrons and, because of excellent conductibility, rapidly transferred photoelectrons from the catalyst interface. Thereby, the photoelectron migration rate and the photogenerated charge separation and the use efficiency of photoelectrons in g-C3N4 were improved, which largely enhanced the hydrogen production ability. Moreover, the addition of CNTs improved the service life and stability of g-C3N4-based photocatalytic H2 production. After 10 hours of visible light irradiation, the maximum H2 yield from the 12-mg/L CNT/g-C3N4 (CG12) was 138.7 times larger than that of g-C3N4 (6548.4 vs 47.2 μmol/g), and the H2 evolution rate was 138.7 times that of g-C3N4 (654.8 vs 4.72 μmol/g/h). After 50 hours, the apparent quantum efficiency of CG12 was up to 37.9%, indicating that the addition of CNTs improved the photocatalytic splitting and stability of g-C3N4. The mechanism of photocatalytic hydrogen production and the roles of CNTs in improving water splitting were discussed through characterization and activity experiments. It was found that the addition of CNTs accelerated the migration, separation, and utilization of photoelectrons and thereby significantly enhanced the photocatalytic performance.
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