Photocatalytic ammonia synthesis from nitrate reduction on nickel single-atom decorated on defective tungsten oxide

被引:19
作者
Wang, Yunlong [1 ,2 ]
Yin, Haibo [2 ]
Zhao, Xiaoguang [1 ]
Qu, Yakun [1 ]
Zheng, Aiguo [1 ]
Zhou, Han [1 ]
Fang, Wei [1 ]
Li, Junhua [2 ]
机构
[1] Sinopec Res Inst Petr Proc Co Ltd, Beijing 100083, Peoples R China
[2] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2024年 / 341卷
基金
芬兰科学院; 中国博士后科学基金; 中国国家自然科学基金;
关键词
Photocatalytic NH 3 synthesis; NO; 3; reduction; Single; -atom; Oxygen vacancies; Orbital hybridizations; ENHANCEMENT; NANOSHEETS; EVOLUTION; CATALYSTS; EFFICIENT;
D O I
10.1016/j.apcatb.2023.123266
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic reduction of waste nitrate (NO3- ) into value-added ammonia (NH3) under ambient conditions has enormous advantages over the Haber-Bosch process. However, weak adsorption capacity and low efficiency of photocatalysts limit its large-scale application. Here, Ni single-atom (SA) on defective WO3 (Ni/HxWO3_y) hybrids with abundant oxygen vacancies (OVs) are synthesized by a facile H-spillover process, which exhibits a high NH3 rate of 10.5 mmol gcat-1 h-1 and 98.26 % NH3 selectivity. In situ characterizations and theoretical calculations demonstrate the activity mainly derives from the synergetic effect of OVs and Ni SAs. That is, (1) photogenerated electrons and adsorbed NO3- transfer from OVs to Ni SAs; (2) the strong hybridizations of Ni 3d O 2p orbitals of NO3- accelerate electron transfer from Ni SAs to NO3- ; (3) Ni SAs effectively reduce the free energy of the rate-limiting step (NO2* -> NO*) of HxWO3_y. In simulated wastewater, the durable performance of Ni/ HxWO3_y hybrids proves great potential in industrial applications.
引用
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页数:9
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