Interfacial Reduction Nucleation of Noble Metal Nanodots on Redox-Active Metal-Organic Frameworks for High-Efficiency Electrocatalytic Conversion of Nitrate to Ammonia

被引:97
|
作者
Jiang, Minghang [1 ,2 ]
Su, Jian [1 ]
Song, Xinmei [1 ]
Zhang, Pengbo [1 ]
Zhu, Mengfei [1 ]
Qin, Lina [1 ]
Tie, Zuoxiu [1 ,2 ]
Zuo, Jing-Lin [1 ]
Jin, Zhong [1 ,2 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem,Jiangsu Key Lab Adv, MOE Key Lab Mesoscop Chem,MOE Key Lab High Perfor, Nanjing 210023, Jiangsu, Peoples R China
[2] Suzhou Tierui New Energy Technol Co Ltd, Suzhou 215228, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Redox-active metal-organic frameworks; Noble metal nanodots; Interfacial reduction nucleation; Electrochemical nitrate reduction; REACTOR;
D O I
10.1021/acs.nanolett.2c00446
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemically converting nitrate to ammonia is a promising route to realize artificial nitrogen recycling. However, developing highly efficient electrocatalysts is an ongoing challenge. Herein, we report the construction of stable and redox-active zirconium metal-organic frameworks (Zr-MOFs) based on Zr-6 nanoclusters and redox-reversible tetrathiafulvalene (TTF) derivatives as inorganic nodes and organic linkers, respectively. The redox-active Zr-MOF can facilitate the in situ reduction of noble metal precursors free of external reductants and realize the uniform nucleation of noble metal nanodots (NDs) on Zr-MOF, achieving the preparation of M-NDs/Zr-MOF (M = Pd, Ag, or Au). The highly porous Zr-MOF with good conductivity can facilitate the mass transfer process. Among the M-NDs/Zr-MOF catalysts, PdNDs/Zr-MOF exhibits the highest electrocatalytic activity, delivering a NH3 yield of 287.31 mmol center dot h(-1)center dot g(-1)cat. and a Faradaic efficiency of 58.1%. The proposed interfacial reduction nucleation strategy for anchoring M NDs on Zr-MOFs can be applied to other challenging energy conversion reactions.
引用
收藏
页码:2529 / 2537
页数:9
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