过电位
材料科学
分解水
制氢
电解水
电催化剂
电解
铂金
催化作用
纳米技术
化学工程
贵金属
金属
电极
光催化
冶金
化学
电化学
电解质
工程类
物理化学
生物化学
作者
William C. Records,Youngmin Yoon,Jacqueline Ohmura,Nicolas Chanut,Angela M. Belcher
出处
期刊:Nano Energy
[Elsevier BV]
日期:2018-12-28
卷期号:58: 167-174
被引量:50
标识
DOI:10.1016/j.nanoen.2018.12.083
摘要
Clean hydrogen production via water electrolysis is incumbent upon the development of high-performing hydrogen evolution reaction electrocatalysts. Despite decades of commercial maturity, however, alkaline water electrolyzers continue to suffer from limitations in electrocatalytic activity and stability, even with noble metal catalysts. In recent years, combining platinum with oxophilic materials, such as metal hydroxides, has shown great promise for improving performance potentially by enabling stronger water dissociation at the surface of electrocatalysts. In this work, we leveraged the nanoscopic proportions and surface programmability of the filamentous M13 bacteriophage in the design, synthesis, and exceptional performance of 3D nanostructured biotemplated electrocatalysts for alkaline hydrogen evolution. We developed a facile synthesis method for phage-templated, Pt–Ni(OH)2 nanonetworks, relying on scalable techniques like electroless deposition. After optimization of the platinum content, our materials display –4.9 A mg–1Pt at −70 mV versus the reversible hydrogen electrode, the highest reported mass activity in 1 M KOH to date, and undergo minimal changes in overpotential under galvanostatic operation at −10 mA cm–2geo. Looking forward, the performance of these catalysts suggests that biotemplating nanostructures with M13 bacteriophage offers an interesting new route for developing high-performing electrocatalysts.
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