塔菲尔方程
过电位
扫描电子显微镜
材料科学
电解质
电极
化学工程
X射线光电子能谱
透射电子显微镜
纳米颗粒
膜
分析化学(期刊)
纳米技术
电化学
复合材料
化学
色谱法
生物化学
工程类
物理化学
作者
Lin Liu,Yu Chen,Jiaojiao Chen,Wenda Liu,Guoxuan Tang,Haocun Wen,Zeyi Xiao,Senqing Fan
标识
DOI:10.1021/acssuschemeng.2c07257
摘要
In order to achieve a balance between a good hydrogen evolution reaction (HER) performance and a low amount of catalyst loading, Pt@Ti membrane self-supporting electrodes have been fabricated by flowing synthesis. The characterizations by X-ray diffraction (XRD), X-ray photoelectric spectroscopy (XPS), and transmission electron microscopy (TEM) demonstrate the successful loading of Pt nanoparticles into the pores of a porous Ti membrane substrate. The scanning electron microscope (SEM) results demonstrate that the sizes of the Pt nanoparticles immobilized in Ti membrane pores are mostly in the range of 10–40 nm, and the average size was about 26 nm. The ICP test proves that the amount of Pt loading was only 0.760 mg cm–2. A minimum overpotential of 35 mV and a minimum Tafel slope of 30 mV dec–1 can be achieved for a Pt@Ti membrane self-supporting electrode at a current density of 10 mA cm–2 with 0.5 M H2SO4 as the electrolyte. No decay of current density is observed after a 10 h continuous electrolytic test. Besides, good HER performances can also be obtained under alkaline conditions and neutral conditions for Pt@Ti membrane self-supporting electrodes fabricated by flowing synthesis.
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