Electro-assisted photocatalytic reduction of CO2 in ambient air using Ag/ TNTAs at the gas-solid interface

被引:3
|
作者
Yue, Feng [1 ]
Fan, Zhaoya [1 ]
Li, Cong [1 ,3 ]
Meng, Yang [1 ]
Zhang, Shuo [1 ]
Shi, Mengke [1 ]
Wang, Minghua [1 ]
Berrettoni, Mario [3 ]
Li, Jun [2 ]
Zhang, Hongzhong [1 ]
机构
[1] Zhengzhou Univ Light Ind, Henan Collaborat Innovat Ctr Environm Pollut Contr, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Henan Inst Adv Technol, Zhengzhou 450052, Peoples R China
[3] Univ Camerino, Dept Chem, I-62032 Camerino, Macerata, Italy
来源
MATERIALS REPORTS: ENERGY | 2024年 / 4卷 / 02期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Electro-assisted photocatalytic; Gas -solid interface; Ambient air; P -N heterojunction; Practical applications; DIOXIDE NANOTUBE ARRAYS; REDUCED GRAPHENE OXIDE; AG2O/TIO2; COMPOSITES; TIO2; HETEROSTRUCTURE; PHOTOREDUCTION; NANOPARTICLES; DEGRADATION; PERFORMANCE; WATER;
D O I
10.1016/j.matre.2024.100269
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The direct conversion of atmospheric CO2 into fuel via photocatalysis exhibits significant practical application value in advancing the carbon cycle. In this study, we established an electro-assisted photocatalytic system with dual compartments and interfaces, and coated Ag nanoparticles on the titanium nanotube arrays (TNTAs) by polydopamine modification. In the absence of sacrificial agent and alkali absorption liquid conditions, the stable, efficient and highly selective conversion of CO2 to CO at the gas-solid interface in ambient air was realized by photoelectric synergy. Specifically, with the assistance of potential, the CO formation rates reached 194.9 mu mol h-1 m-2 and 103.9 mu mol h-1 m-2 under ultraviolet and visible light irradiation, respectively; the corresponding CO2 conversion rates in ambient air were 30% and 16%, respectively. The excellent catalytic effect is mainly attributed to the formation of P-N heterojunction during the catalytic process and the surface plasmon resonance effect. Additionally, the introduction of solid agar electrolytes effectively inhibits the hydrogen evolution reaction and improves the electron utilization rate. This system promotes the development of photocatalytic technology for practical applications and provides new insights and support for the carbon cycle.
引用
收藏
页数:12
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