光催化
硝酸盐
吸附
镍
材料科学
电子转移
氨
氧化物
钨
无机化学
速率决定步骤
光化学
化学
催化作用
物理化学
冶金
有机化学
作者
Yunlong Wang,Haibo Yin,Xiaoguang Zhao,Yakun Qu,Aiguo Zheng,Han Zhou,Wei Fang,Junhua Li
标识
DOI:10.1016/j.apcatb.2023.123266
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.
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