贵金属
成核
氧化还原
纳米团簇
金属有机骨架
催化作用
材料科学
无机化学
锆
化学工程
法拉第效率
纳米点
金属
化学
电化学
纳米技术
吸附
有机化学
电极
物理化学
冶金
工程类
作者
Minghang Jiang,Jian Su,Xinmei Song,Pengbo Zhang,Mengfei Zhu,Lina Qin,Zuoxiu Tie,Jing‐Lin Zuo,Zhong Jin
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-03-10
卷期号:22 (6): 2529-2537
被引量:126
标识
DOI:10.1021/acs.nanolett.2c00446
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 Zr6 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, Pd-NDs/Zr-MOF exhibits the highest electrocatalytic activity, delivering a NH3 yield of 287.31 mmol·h-1·g-1cat. 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.
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