光催化
材料科学
石墨氮化碳
纳米纤维
碳纳米管
化学工程
氮化碳
催化作用
纳米技术
氢
氮化物
化学气相沉积
化学
有机化学
工程类
图层(电子)
作者
Xiaobo Wu,Huiqing Fan,Weijia Wang,Lin Lei,Xinye Chang
标识
DOI:10.1021/acsaem.1c02846
摘要
Metal-free graphitic carbon nitride (g-C 3 N 4 ) has become one of the most up-and-coming photocatalyst candidates for the hydrogen evolution reaction. However, the improvement in photocatalytic property is strongly suppressed by the limited active reaction sites due to the bulk microstructure of g-C 3 N 4 . On this basis, we exploit a moderate and economical approach to prepare an ordered and one-dimensionally ultralong carbon nitride nanotube (CN-NT) via the in-air chemical vapor deposition (CVD) with SiO 2 nanofiber templates synthesized by electrostatic spinning. Due to the uniform size, fluffiness, and easy removal, SiO 2 nanofiber templates are conducive to prepare ordered and tubular CN-NT. The obtained CN-NT sample exhibits an excellent photocatalytic hydrogen evolution rate (HER) of 4605.2 μmol·h –1 ·g –1 under visible light, which is 33.4 times higher than that of the original bulk g-C 3 N 4 . The apparent quantum efficiency reaches 6.49% at 420 nm. The enhancement in the photocatalytic activity is ascribed to the increased specific surface area, faster electron transfer pathway, advanced light absorption ability, and furthermore the lower recombination rate of photogenerated electrons.
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