Amorphous NiOn coupled with trace PtOx toward superior electrocatalytic overall water splitting in alkaline seawater media

被引:0
作者
Yu, Wenli [1 ,2 ]
Liu, Hongru [2 ]
Zhao, Ying [2 ]
Fu, Yunlei [2 ]
Xiao, Weiping [3 ]
Dong, Bin [1 ]
Wu, Zexing [2 ]
Chai, Yongming [1 ]
Wang, Lei [2 ]
机构
[1] China Univ Petr East China, Coll Sci, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Key Lab Ecochem Engn, Minist Educ,Int Sci & Technol Cooperat Base Ecoche, Qingdao 266042, Peoples R China
[3] Nanjing Forestry Univ, Coll Sci, Nanjing 210037, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
hydrogen; oxygen evolution reaction; alkaline seawater splitting; amorphous structure; ultralow Pt electrocatalyst; HYDROGEN EVOLUTION; DOMINATING ROLE; NICKEL; NANOPARTICLES; PERFORMANCE; ULTRAFINE; FACILE; ARRAYS; REDUCTION; INTERFACE;
D O I
暂无
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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 center dot 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 center dot 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 center dot 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.
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页数:14
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