Solvent dispersion triggered the formation of NiFe-gel as an efficient electrocatalyst for enhancing the oxygen evolution reaction

2020 ◽  
Vol 56 (56) ◽  
pp. 7781-7784
Author(s):  
Hongkai Wang ◽  
Weihuang Zhu ◽  
Qi Xue ◽  
Changhao Wang ◽  
Kaiqiang Liu

The solvent dispersion triggered gelation for a Ni2.0Fe-gel catalyst has a specific surface area of 216.9 m2 g−1, and its overpotential in an alkaline electrolyte can reach a lower value with 245 mV at 10 mA cm−2 than commercial metal RuO2.

Nanoscale ◽  
2017 ◽  
Vol 9 (27) ◽  
pp. 9291-9298 ◽  
Author(s):  
Guoqiang Li ◽  
Songtao Li ◽  
Meiling Xiao ◽  
Junjie Ge ◽  
Changpeng Liu ◽  
...  

Micro/mesoporous IrO2 catalyst with an ultrahigh specific surface area of 363.3 m2 g−1 shows excellent electrocatalytic performance for the oxygen evolution reaction.


2020 ◽  
Vol 10 (22) ◽  
pp. 7566-7580
Author(s):  
Pei-Sung Hung ◽  
Wei-An Chung ◽  
Shih-Cheng Chou ◽  
Kuang-Chih Tso ◽  
Chung-Kai Chang ◽  
...  

The inverse opals exhibit a 3D ordered macroporous framework, which provides an excessive surface area and facile mass transport. A conformal NiCoOx functional coating further renders these materials with increased reactivity in OER catalysis.


2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Yugan Gao ◽  
Chengqi Wu ◽  
Sen Yang ◽  
Yiwei Tan

Abstract The oxygen evolution reaction is an essential factor in many renewable energy technologies, such as water splitting, fuel cells, and metal–air batteries. Here we show a unique solution to improve the oxygen evolution reaction rate by adjusting the electrolyte composition via the introduction of hexadecyltrimethylammonium hydroxide into an alkaline electrolyte. The strong adsorption of hexadecyltrimethylammonium cations on the surface of electrocatalysts provides the increased absolute number of OH− ions near the electrocatalyst surface, which effectively promotes the oxygen evolution reaction performance of electrocatalysts, such as Fe1−yNiyS2@Fe1−xNixOOH microplatelets and SrBaNi2Fe12O22 powders. Meanwhile, we present an electrochemical conditioning approach to engineering the electrochemically active surface area of electrocatalysts, by which the resultant Fe1−yNiyS2@Fe1−xNixOOH microplatelets have a larger electrochemically active surface area after the electrochemical conditioning of the as-synthesized Fe1−yNiyS2 microplatelets using ammonia borane than those obtained after the conventional electrochemical conditioning without ammonia borane, presumably due to the appropriate conversion rate of Fe1−xNixOOH shells.


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