电催化剂
双功能
分解水
材料科学
析氧
化学工程
电极
无定形固体
氧化物
电解质
电解
纳米技术
无机化学
化学
电化学
催化作用
冶金
物理化学
结晶学
有机化学
光催化
工程类
作者
Wen‐Li Yu,Hongru Liu,Ying Zhao,Yunlei Fu,Weiping Xiao,Bin Dong,Zexing Wu,Yong‐Ming Chai,Lei Wang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-01-21
卷期号:16 (5): 6517-6530
被引量:35
标识
DOI:10.1007/s12274-022-5369-0
摘要
Developing corrosion resistance bifunctional electrocatalysts with high activity and stability toward both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), especially electrolysis in seawater, is of prime significance but still pressingly challenging. Herein, in-situ introduced PtOx on the derivative amorphous NiOn is prepared via heat treatment of Ni ZIF-L nanosheets on nickel foam under low temperature (PtOx−NiOn/NF). The synthesized PtOx−NiOn/NF possesses suprahydrophilic and aerophilic surface, and then in favor of intimate contact between the electrode and electrolyte and release of the generated gas bubbles during the electrocatalysis. As a result, the in-situ PtOx−NiOn/NF electrode presents outstanding bifunctional activity, which only requires extremely low overpotentials of 32 and 240 mV to reach a current density of 10 mA·cm−2 for HER and OER, respectively, which exceeds most of the electrocatalysts previously developed and even suppresses commercial Pt/C and RuO2 electrodes. As for two-electrode cell organized by PtOx−NiOn/NF, the voltages down to 1.57 and 1.58 V are necessary to drive 10 mA·cm−2 with remarkable durability in 1 M KOH and alkaline seawater, respectively, along with remarkable stability. Moreover, a low cell voltage of 1.88 V is needed to achieve 1,000 mA·cm−2 toward water-splitting under industrial conditions. This study provides a new idea for designing in-situ amorphous metal oxide bifunctional electrocatalyst with strong Pt-support interaction for overall water splitting.
科研通智能强力驱动
Strongly Powered by AbleSci AI