异质结
石墨氮化碳
光催化
氮化碳
还原(数学)
兴奋剂
材料科学
氮化物
碳纤维
光电子学
化学
纳米技术
催化作用
复合数
复合材料
数学
生物化学
几何学
图层(电子)
作者
Sijie Wan,Yan-Ting Hou,Wang Wang,Guoqiang Luo,Chuanbin Wang,Rong Tu,Shaowen Cao
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2024-07-06
卷期号:43 (11): 5880-5890
被引量:44
标识
DOI:10.1007/s12598-024-02861-z
摘要
Abstract Photocatalytic reduction of CO 2 has attracted considerable interest owing to its potential to resolve the energy and environmental problems. Nevertheless, the lack of proficient photocatalysts has restricted the application of solar‐driven photocatalytic CO 2 reduction. Herein, we reported an S‐scheme heterojunction by combining g‐C 3 N 4 with La 3+ and Rh 3+ co‐doped SrTiO 3 through the electrostatic self‐assembly method for the efficient photocatalytic CO 2 reduction. In comparison with g‐C 3 N 4 , the as‐prepared CN/LRSTO‐30 wt% S‐scheme heterojunction not only possesses a broadened visible‐light response due to the defect states in La, Rh co‐doped SrTiO 3 induced by co‐doped La 3+ and Rh 3+ but also has more adsorption sites for the capture and activation of CO 2 molecules. Additionally, separation and transfer efficiency of the photoinduced charge carriers is much enhanced in the CN/LRSTO‐30 wt% S‐scheme heterojunction via its robust internal electric field, which is firmly demonstrated by in situ irradiation X‐ray photoelectron spectroscopy technology. Consequently, the prepared S‐scheme heterojunction achieves impressive photocatalytic CO 2 reduction performance with an average CO and CH 4 evolution rate of 4.1–1.8 μmol·g −1 ·h −1 , respectively, which are ~ 1.9 and ~ 22.5‐fold higher than those of pure g‐C 3 N 4 . This study provides innovative perspectives on the design of creative S‐scheme heterojunctions for applications in photocatalytic CO 2 reduction.
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