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Platinum/Platinum Sulfide on Sulfur-Doped Carbon Nanosheets with Multiple Interfaces toward High Hydrogen Evolution Activity
被引:1
作者:
Zhang, Mou
[1
]
Su, Mengfei
[1
]
Zhang, Chunyan
[1
]
Gao, Feng
[2
]
Lu, Qingyi
[1
]
机构:
[1] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, State Key Lab Coordinat Chem, Coordinat Chem Inst,Sch Chem & Chem Engn, Nanjing 210023, Peoples R China
[2] Nanjing Univ, Coll Engn & Appl Sci, Collaborat Innovat Ctr Adv Microstruct, Jiangsu Key Lab Artificial Funct Mat,Dept Mat Sci, Nanjing 210023, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
platinum/platinum sulfide;
heterogeneous interface;
doping;
hydrogen evolution reaction;
NANOPARTICLES;
GRAPHENE;
D O I:
10.3390/molecules29194570
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
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 degrees 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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