光催化
光化学
电子转移
材料科学
碳纤维
可见光谱
分解水
电子密度
产量(工程)
电子
带隙
催化作用
化学物理
纳米技术
化学
光电子学
物理
有机化学
复合材料
量子力学
冶金
复合数
作者
Xue Ou,Xinrui Chen,Siyu Zhao,Yarong Shi,Junhua Zhang,Min Wu,Arthur J. Ragauskas,Xueping Song,Zhanying Zhang
出处
期刊:Small
[Wiley]
日期:2024-12-19
卷期号:21 (6): e2408200-e2408200
被引量:14
标识
DOI:10.1002/smll.202408200
摘要
Carbon dots (CDs) have a wide light absorption range, which are promising candidates for photocatalytic water splitting H2 evolution, but they show low activity for hydrogen evolution reaction (HER) due to the slow transfer efficiencies of photogenerated carriers. The electron cloud density of photocatalyst is essential for the separation and migration of photogenerated carriers. In this study, the effect mechanism of electron cloud density regulated by the substituents with different electronic effects on the photocatalytic HER of glucose-based CDs is clarified. CDs-SO3H and CDs-OH are first obtained by introducing electron-drawing group (─SO3H) and electron-donating group (─OH) using a tailoring post-processing strategy. Experimental results show that the H2 yield catalyzed by CDs-SO3H is 89.95 µmol•g-1 in 4 h, which is about four times that of CDs, and 7.4 times that of CDs-OH. The ─SO3H induces a much negative energy band and high electron cloud density on CDs edges, promoting the separation and transfer of photogenerated carriers; while the CDs-OH exhibits a high positive charge density and an upward energy band, hindering the surface complexation of electron-hole pairs and HER. This study will provide an insight into the design of CDs catalysts with efficient photocatalytic HER at a molecular level.
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