过电位
塔菲尔方程
铂金
催化作用
材料科学
化学工程
碳纤维
吸附
硫黄
无机化学
纳米技术
化学
电化学
物理化学
有机化学
电极
复合材料
冶金
复合数
工程类
作者
Mou Zhang,Mengfei Su,Chunyan Zhang,Feng Gao,Qingyi Lu
出处
期刊:Molecules
[MDPI AG]
日期:2024-09-26
卷期号:29 (19): 4570-4570
被引量:1
标识
DOI:10.3390/molecules29194570
摘要
Platinum (Pt)-based materials are among the most competitive electrocatalysts for the hydrogen evolution reaction (HER) due to suitable hydrogen adsorption energy. Due to the rarity of Pt, it is desirable to develop cost-effective Pt-based electrocatalysts with low Pt loading. Herein, Pt/PtS electrocatalysts on S-doped carbon nanofilms (PPS/C) have been successfully fabricated through a precursor reduction route with a complex of Pt and 1-dodecanethiol (1-DDT) as the precursor. The PPS/C achieved at 400 °C (PPS/C-400) exhibits excellent HER performances with an ultralow overpotential of 41.3 mV, a low Tafel slope of 43.1 mV dec−1 at a current density of 10 mA cm−2, and a long-term stability of 10 h, superior to many recently reported Pt-based HER electrocatalysts. More importantly, PPS/C-400 shows a high mass-specific activity of 0.362 A mgPt−1 at 30 mV, which is 1.88 times of that of commercial 20% Pt/C (0.193 A mgPt−1). The introduction of sulfur leads to the formation of PtS, which not only reduces the content of Pt but also realizes the interface regulation of Pt/PtS, as well as the doping of carbon. Both regulations make the resulting catalyst have abundant active centers and rapid electron transfer/transport, which is conducive to balancing the adsorption and resolution of intermediate products, and finally achieving great mass-specific activity and stability. The research work may provide ideas for designing effective Pt-based multi-interface electrocatalysts.
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