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作 者:Longqi Zhu Runze Wang Chen Wang Shuhan Yang Haizhen Liu Bo Xing Honghui Cheng Kuikui Wang
机构地区:[1]Institute of Materials for Energy and Environment,Laboratory of New Fiber Materials and Modern Textile,Growing Basis for State Key Laboratory,College of Materials Science and Engineering,Qingdao University,Qingdao 266071,China [2]MOE Key Laboratory of New Processing Technology for Non-ferrous Metals and Materials,Guangxi Key Laboratory of Processing for Non-ferrous Metals and Featured Materials,Guangxi University,Nanning 530004,China [3]National Engineering Laboratory of Circular Economy,Sichuan University of Science and Engineering,Zigong 643000,China [4]School of Mechanical Engineering,Yangzhou University,Yangzhou 225127,China [5]Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology,Changzhou University,Changzhou 213164,China
出 处:《ChemPhysMater》2025年第1期78-85,共8页化学物理材料(英文)
基 金:financial support provided by the National Natural Science Foundation of China(51801108);the Shandong Provincial Natural Science Foundation(ZR2023ME072);the Key Research and Development Program of Shandong Province(2019GGX103048);support from the Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology(BM2012110);the Open Foundation of Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials(2022GXYSOF16);the Open Fundation of the National Engineering Laboratory of Circular Economy at Sichuan University of Science and Engineering(XHJJ-2304).
摘 要:Metal-cation doping is a fundamental strategy for enhancing catalyst performance.Fe-doped Ni_(0.85)Se/NF(Fe-Ni_(0.85)Se/NF)nanoparticles were prepared at 80°C via Fe^(2+)etching method.The addition of Fe altered the coordination environment of the Ni species along with the catalyst's morphology,creating additional active sites.Notably,the synergistic interaction between the bimetallic components augmented the built-in activity and accelerated reaction kinetics.The Fe-Ni_(0.85)Se/NF electrocatalysts demonstrated remarkable catalytic activity for the oxygen evolution reaction(OER),with an acceptable overpotential of 276 mV and a Tafel slope of 58.1 mV dec^(−1)at 100 mA cm^(−2).Moreover,they demonstrated exceptional durability.In situ Raman and X-ray photoelectron spectroscopy(XPS)analyses showed that the excellent OER performance stemmed from the reconstruction-induced hydroxyl oxide.This study offers a novel approach for streamlining the synthesis procedures and reducing the experimental costs for developing high-efficiency electrocatalysts.
关 键 词:DOPING Selenylation Hydrothermal reaction Oxygen evolution reaction ELECTROCATALYSTS
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