Intensifying Interfacial Reverse Hydrogen Spillover for Boosted Electrocatalytic Nitrate Reduction to Ammonia

被引:3
|
作者
Ouyang, Xiao [1 ]
Qiao, Wei [1 ]
Yang, Yuting [1 ]
Xi, Baojuan [2 ]
Yu, Yu [3 ]
Wu, Yilu [1 ]
Fang, Jingyun [1 ]
Li, Ping [1 ]
Xiong, Shenglin [2 ]
机构
[1] Sun Yat Sen Zhongshan Univ, Sch Environm Sci & Engn, Guangdong Prov Key Lab Environm Pollut Control & R, Guangzhou 510275, Peoples R China
[2] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[3] Beijing Jiaotong Univ, Dept Mat & Engn, Beijing 100044, Peoples R China
基金
中国国家自然科学基金;
关键词
reverse hydrogen spillover; active hydrogen; electronic metal-support interaction; electrochemical nitrate reduction; zinc-nitrate battery; EVOLUTION;
D O I
10.1002/anie.202422585
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rational regulation of active hydrogen (*H) behavior is crucial for advancing electrocatalytic nitrate reduction reaction (NO3RR) to ammonia (NH3), yet in-depth understanding of the *H generation, transfer, and utilization remains ambiguous, and explorations for *H dynamic optimization are urgently needed. Herein we engineer a Ni3N nanosheet array intimately decorated with Cu nanoclusters (NF/Ni3N-Cu) for remarkably boosted NO3RR. From comprehensive experimental and theoretical investigations, the Ni3N moieties favors water dissociation to generate *H, and then *H can rapidly transfer to the Cu via unique reverse hydrogen spillover mediating interfacial Ni-N-Cu bridge bond, thus increasing *H coverage on the Cu site for subsequent deoxygenation/hydrogenation. More impressively, such intriguing reverse hydrogen spillover effect can be further strengthened via elegant engineering of the Ni3N/Cu heterointerface with more intimate contact. Consequently, the NF/Ni3N-Cu with Cu nanoclusters intimate anchoring presents record NH3 yield rate of 1.19 mmol h-1 cm-2 and Faradaic efficiency of 98.7 % at -0.3 V vs. RHE, being on par with the state-of-the-art ones. Additionally, with NF/Ni3N-Cu as the cathode, a high-performing Zn-NO3- battery can be assembled. This contribution illuminates a novel pathway to optimize *H behavior via distinct reverse hydrogen spillover for promoted NO3RR and other hydrogenation reactions.
引用
收藏
页数:13
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