过电位
介孔材料
化学工程
材料科学
催化作用
析氧
电催化剂
纳米材料
X射线光电子能谱
无机化学
可逆氢电极
氧化物
分解水
纳米颗粒
光催化
电化学
纳米技术
化学
电极
工作电极
工程类
物理化学
生物化学
冶金
作者
Piyali Bhanja,Bishnupad Mohanty,Astam K. Patra,Soumen Ghosh,Bikash Kumar Jena,Asim Bhaumik
出处
期刊:Chemcatchem
[Wiley]
日期:2018-10-19
卷期号:11 (1): 583-592
被引量:99
标识
DOI:10.1002/cctc.201801312
摘要
Abstract Electrocatalytic hydrogen and oxygen evolutions via water splitting are very demanding in the context of renewable energy and sustainable environment. We first report the synthesis of wormhole‐like mesoporous tin oxide (MTO‐S) by using sodium lauroyl sarcosinate as structure directing agent under hydrothermal reaction conditions followed by calcination and loading with IrO 2 or Pt nanoparticles at its surface by simple wet‐chemical methods. These IrO 2 and Pt‐loaded SnO 2 nanomaterials are thoroughly characterized by small and wide‐angle powder XRD, nitrogen adsorption/desorption analysis, FTIR, XPS spectroscopy, UHR‐TEM, FE‐SEM, TG/DTA and NH 3 ‐TPD analysis. The electrochemical water splitting measurements of the IrO 2 and Pt doped mesoporous SnO 2 nanostructured materials suggested fine dispersion of these metal/metal oxide nanoparticles at the mesopore surface and facile electron hopping could enhance the rate of the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) activity of IrO 2 @MTO‐S and Pt@MTO‐S nanocomposites, respectively. As a result, the IrO 2 @MTO‐S modified electrode exhibits unprecedented OER activity with a very low overpotential of 240 mV at 10 mA cm −2 , which is lower than the state‐of‐the‐art catalyst IrO 2 /C (360 mV) and other reported catalysis. Pt@MTO‐S also exhibit excellent HER activity with an ultralow overpotential of 73 mV at 10 mA cm −2 . These findings may uncover new opportunities for IrO 2 @MTO‐S and Pt@MTO‐S as OER and HER electrocatalysts for future water electrolysis.
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