淡江大學機構典藏:Item 987654321/111869
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    題名: In situ evolution of highly-dispersed amorphous CoOx cluster for oxygen evolution reaction
    作者: Dawei Chen;Chung-Li Dong;Yuqin Zou;Dong Su;Yu-Cheng Huang;Li Tao;Shuo Dou;Shaohua Shen;Shuangyin Wang
    日期: 2017-07-24
    上傳時間: 2017-10-27 02:11:15 (UTC+8)
    出版者: Royal Society of Chemistry
    摘要: Electrocatalytic water splitting is a key technique to produce hydrogen fuels, which can be considered as an efficient strategy to store renewable energy. Oxygen evolution reaction (OER) that occurs at the anode side requires a four-electron transfer under highly oxidizing conditions. OER has a large overpotential and therefore determines the overall efficiency. Certain electrocatalysts can efficiently help to improve the reaction kinetics. Owing to the high cost of precious metals such as Pt, Ru, and Ir, non-precious metal oxide catalysts have been vigorously investigated under alkaline conditions. Herein, we synthesized novel highly dispersed amorphous CoOxfor the first time in the form of a cluster favorable to enhance the OER activity using a facile method via the air dielectric barrier discharge (DBD) plasma. Compared with the pristine biopolymer–cobalt complex, the amorphous CoOx cluster exhibits a much higher current density and a lower overpotential for OER, e.g., the overpotential of 290 mV at 10 mA cm−2 and the overpotential of only 350 mV at 300 mA cm−1. The excellent electrocatalytic OER activity was attributed to the unsaturated catalytic sites on the amorphous CoOx cluster. In addition, we studied the reaction mechanism, and it was observed that pure O2 DBD plasma could lead to the evolution of crystalline CoOx; however, the presence of N2 and O2 in DBD plasma could ensure the facile evolution of amorphous CoOx clusters. This study provides a new strategy to design amorphous materials for electrocatalysis and beyond.
    關聯: Nanoscale 9, p.11969-11975
    DOI: 10.1039/C7NR04381C
    顯示於類別:[物理學系暨研究所] 期刊論文

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