光催化
纳米棒
氮化碳
异质结
材料科学
制氢
分解水
硒化镉
量子点
二氧化碳电化学还原
太阳能燃料
载流子
量子效率
量子产额
光化学
人工光合作用
化学工程
纳米技术
氢
光电子学
化学
催化作用
有机化学
光学
物理
工程类
一氧化碳
荧光
作者
Ya‐Yun Wang,Haotian Wang,Yuke Li,Mingwen Zhang,Yun Zheng
出处
期刊:Molecules
[MDPI AG]
日期:2022-09-23
卷期号:27 (19): 6286-6286
被引量:9
标识
DOI:10.3390/molecules27196286
摘要
Constructing photocatalysts to promote hydrogen evolution and carbon dioxide photoreduction into solar fuels is of vital importance. The design and establishment of an S-scheme heterojunction system is one of the most feasible approaches to facilitate the separation and transfer of photogenerated charge carriers and obtain powerful photoredox capabilities for boosting photocatalytic performance. Herein, a zero-dimensional/one-dimensional S-scheme heterojunction composed of CdSe quantum dots and polymeric carbon nitride nanorods (CdSe/CN) is created and constructed via a linker-assisted hybridization approach. The CdSe/CN composites exhibit superior photocatalytic activity in water splitting and promoted carbon dioxide conversion performance compared with CN nanorods and CdSe quantum dots. The best efficiency in photocatalytic water splitting (10.2% apparent quantum yield at 420 nm irradiation, 20.1 mmol g-1 h-1 hydrogen evolution rate) and CO2 reduction (0.77 mmol g-1 h-1 CO production rate) was achieved by 5%CdSe/CN composites. The significantly improved photocatalytic reactivity of CdSe/CN composites primarily originates from the emergence of an internal electric field in the zero-dimensional/one-dimensional S-scheme heterojunction, which could greatly improve the photoinduced charge-carrier separation. This work underlines the possibility of employing polymeric carbon nitride nanostructures as appropriate platforms to establish highly active S-scheme heterojunction photocatalysts for solar fuel production.
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