A general synthesis approach for amorphous noble metal nanosheets

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作者
Geng Wu
Xusheng Zheng
Peixin Cui
Hongyu Jiang
Xiaoqian Wang
Yunteng Qu
Wenxing Chen
Yue Lin
Hai Li
Xiao Han
Yanmin Hu
Peigen Liu
Qinghua Zhang
Jingjie Ge
Yancai Yao
Rongbo Sun
Yuen Wu
Lin Gu
Xun Hong
Yadong Li
机构
[1] University of Science and Technology of China,Hefei National Laboratory for Physical Sciences at the Microscale, Department of Applied Chemistry, Center of Advanced Nanocatalysis (CAN)
[2] University of Science and Technology of China,National Synchrotron Radiation Laboratory (NSRL)
[3] Chinese Academy of Sciences,Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science
[4] Chinese Academy of Sciences,Institute of Physics
[5] Beijing Institute of Technology,Beijing Key Laboratory of Construction Tailorable Advanced Functional Materials and Green Applications, School of Materials Science and Engineering
[6] University of Science and Technology of China,Hefei National Laboratory for Physical Sciences at the Microscale
[7] Nanjing Technology University,Key Laboratory of Flexible Electronics (KLOFE) and Institute of Advanced Materials (IAM), Jiangsu National Synergetic In
[8] Tsinghua University,novation Center for Advanced Materials (SICAM)
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摘要
Noble metal nanomaterials have been widely used as catalysts. Common techniques for the synthesis of noble metal often result in crystalline nanostructures. The synthesis of amorphous noble metal nanostructures remains a substantial challenge. We present a general route for preparing dozens of different amorphous noble metal nanosheets with thickness less than 10 nm by directly annealing the mixture of metal acetylacetonate and alkali salts. Tuning atom arrangement of the noble metals enables to optimize their catalytic properties. Amorphous Ir nanosheets exhibit a superior performance for oxygen evolution reaction under acidic media, achieving 2.5-fold, 17.6-fold improvement in mass activity (at 1.53 V vs. reversible hydrogen electrode) over crystalline Ir nanosheets and commercial IrO2 catalyst, respectively. In situ X-ray absorption fine structure spectra indicate the valance state of Ir increased to less than + 4 during the oxygen evolution reaction process and recover to its initial state after the reaction.
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