材料科学
光催化
石墨氮化碳
选择性
异质结
氮化碳
氢氧化物
石墨
氧化还原
化学工程
催化作用
载流子
Zeta电位
纳米技术
光电子学
复合材料
化学
有机化学
纳米颗粒
冶金
工程类
作者
Anqi Zhou,Jinman Yang,Xingwang Zhu,Xianglin Zhu,Jinyuan Liu,Kang Zhong,Han-Xiang Chen,Jinyu Chu,Yansheng Du,Yanhua Song,Junchao Qian,Huaming Li,Hui Xu
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2022-03-14
卷期号:41 (6): 2118-2128
被引量:109
标识
DOI:10.1007/s12598-022-01960-z
摘要
Abstract Graphite phase carbon nitride (g‐C 3 N 4 ) is a promising catalyst for artificial photocatalytic carbon dioxide (CO 2 ) reduction. However, the fast carrier recombination and the inadequacy of the CO 2 reduction active site in g‐C 3 N 4 block the escalation of the performance. In this work, NiCo layered double hydroxide (NiCo LDH) nanoflowers were self‐assembled with ultrathin graphite phase carbon nitride (g‐C 3 N 4 ) by an ultrasonic stirring strategy utilizing the Zeta potential difference. The formed NiCo LDH/ultrathin g‐C 3 N 4 nanosheets (LDH‐CN) photocatalysts own the merits of rich active sites and Z‐scheme heterojunction, which lead to the enhanced CO 2 reduction activity and selectivity. The highest yields of CO and CH 4 were 114.24 and 26.48 μmol·h −1 ·g −1 , which were much greater than those of g‐C 3 N 4 and LDH. Meanwhile, the enhanced selectivity for CO confirmed the strong redox ability in the LDH‐CN caused by the Z‐scheme. The heterojunction‐induced built‐in electrical field can promote the separation and migration of photoinduced electrons and holes. This study provides a theoretical basis for designing high‐performance photocatalysts.
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