光催化
异质结
纳米颗粒
材料科学
可见光谱
热液循环
试剂
纳米技术
光化学
化学工程
催化作用
光电子学
化学
物理化学
有机化学
工程类
作者
Peiling Lin,Lujiang Xiao,Ying Lü,Zizhong Zhang,Xuxu Wang,Wenyue Su
出处
期刊:Chemcatchem
[Wiley]
日期:2022-09-14
卷期号:14 (21)
被引量:8
标识
DOI:10.1002/cctc.202201041
摘要
Abstract The efficiency of photocatalytic reduction of CO 2 with water to hydrocarbons is largely limited by high recombination rate of photogenerated electrons and holes in the photocatalysts. Herein, 0D/2D CeO 2 /LaTiO 2 N S‐scheme heterojunction photocatalyst prepared by simple in‐situ hydrothermal approach realizes the overall conversion of gaseous CO 2 and H 2 O without any sacrificial reagent and cocatalyst. The yields of CH 4 and CO over CeO 2 /LaTiO 2 N sample under visible light for 3 h are 1.5 and 7.2 μmol g −1 , and the corresponding utilized photoelectron number (UPN) is 26.4 μmol g −1 , about 7.3 and 7.8 times that of individual LaTiO 2 N and CeO 2 , respectively. The enhanced photocatalytic activity of 0D/2D CeO 2 /LaTiO 2 N is attributed to the constitution of the S‐scheme heterojunction, which effectively inhibits the recombination of photogenerated carriers. This study is expected to provide a new insight into the construction of efficient 0D/2D photocatalysts for visible‐light‐driven photocatalytic CO 2 reduction.
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