An Li, Huang Bolong, Zhang Yu, Wang Rui, Zhang Nan, Dai Tengyuan, Xi Pinxian, Yan Chun-Hua
State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, China.
Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Hum, Kowloon, Hong Kong SAR, China.
Angew Chem Int Ed Engl. 2019 Jul 8;58(28):9459-9463. doi: 10.1002/anie.201903879. Epub 2019 Jun 5.
Atomic-thick interfacial dominated bifunctional catalyst NiO/CoO transition interfacial nanowires (TINWs) with abundant defect sites display high electroactivity and durability in the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR). Density functional theory (DFT) calculations show that the excellent OER/ORR performance arises from the electron-rich interfacial region coupled with defect sites, thus enabling a fast-redox rate with lower activation barrier for fast electron transfer. When assembled as an air-electrode, NiO/CoO TINWs delivered the high specific capacity of 842.58 mAh g , the large energy density of 996.44 Wh kg with long-time stability of more than 33 h (25 °C), and superior performance at low (-10 °C) and high temperature (80 °C).
具有大量缺陷位点的原子级厚度界面主导双功能催化剂NiO/CoO过渡界面纳米线(TINWs)在析氧反应(OER)和氧还原反应(ORR)中表现出高电活性和耐久性。密度泛函理论(DFT)计算表明,优异的OER/ORR性能源于富含电子的界面区域与缺陷位点的耦合,从而实现了具有较低活化能垒的快速氧化还原速率,有利于快速电子转移。当组装成空气电极时,NiO/CoO TINWs具有842.58 mAh g的高比容量、996.44 Wh kg的大能量密度,在25°C下具有超过33小时的长期稳定性,并且在低温(-10°C)和高温(80°C)下表现优异。