碳纤维
微型多孔材料
材料科学
催化作用
石墨烯
热解
硫脲
甲醇
金属
电解质
无机化学
坩埚(大地测量学)
氧气
氮气
化学工程
纳米技术
化学
有机化学
电极
冶金
复合数
复合材料
物理化学
计算化学
工程类
作者
Xiao-wen Ye,Libing Hu,Mincong Liu,Gang Wang,Feng Ye
标识
DOI:10.1016/s1872-5805(20)60506-6
摘要
Rationally designing and optimizing metal-free electrocatalysts for the oxygen reduction reaction (ORR) isof great importance for fuel cells and metal-air batteries, but remains a great challenge. A N,S-codoped graphene-like carbon (GLC) was synthesized by a simple carbon-bath pyrolysis method, in which urea and thiourea (1:1 w/w) were used as both the sacrificial template and source of nitrogen and sulfur, and glucose as the carbon precursor. A mixture of these materials was placed in a crucible that was contained in a larger crucible full of carbon powder. Compared with N-doped or S-doped GLCs synthesized using only urea or thiourea, respectively, the N,S-codoped GLC had a pore volume of 0.63 cm3/g and a larger specific surface area of 583.68 m2/g, the highest micropore to total surface area of 29.39% and micropore to total pore volume of 12.70%, and the highest pyridinic-N and graphitic-N content of up to 92.2%.The N,S-codoped GLC showeda high electrocatalytic activity for ORR with a mid-wave potential (E1/2) of 0.82 VRHE, which was more positive than that of Pt/C (E1/2=0.80 VRHE) in an alkaline electrolyte. The N,S-codoped GLC catalyst had better stability and superior methanol tolerance compared with commercial Pt/C (20 wt%), abenchmark catalyst.
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