过电位
析氧
电催化剂
催化作用
石墨烯
材料科学
钴
无机化学
硫化钴
电化学
分解水
电解质
化学工程
化学
纳米技术
电极
有机化学
物理化学
工程类
光催化
作者
Nan Wang,Ligui Li,Dengke Zhao,Xiongwu Kang,Zhenghua Tang,Shaowei Chen
出处
期刊:Small
[Wiley]
日期:2017-07-10
卷期号:13 (33)
被引量:120
标识
DOI:10.1002/smll.201701025
摘要
Nitrogen and sulfur‐codoped graphene composites with Co 9 S 8 (NS/rGO‐Co) are synthesized by facile thermal annealing of graphene oxides with cobalt nitrate and thiourea in an ammonium atmosphere. Significantly, in 0.1 m KOH aqueous solution the best sample exhibits an oxygen evolution reaction (OER) activity that is superior to that of benchmark RuO 2 catalysts, an oxygen reduction reaction (ORR) activity that is comparable to that of commercial Pt/C, and an overpotential of only −0.193 V to reach 10 mA cm −2 for hydrogen evolution reaction (HER). With this single catalyst for oxygen reversible electrocatalysis, a potential difference of only 0.700 V is observed in 0.1 m KOH solution between the half‐wave potential in ORR and the potential to reach 10 mA cm −2 in OER; in addition, an overpotential of only 450 mV is needed to reach 10 mA cm −2 for full water splitting in the same electrolyte. The present trifunctional catalytic activities are markedly better than leading results reported in recent literature, where the remarkable trifunctional activity is attributed to the synergetic effects between N,S‐codoped rGO, and Co 9 S 8 nanoparticles. These results highlight the significance of deliberate structural engineering in the preparation of multifunctional electrocatalysts for versatile electrochemical reactions.
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