标题
作者
作者:Wang, J (Wang, Jiong)[1 ]; Gan, LY (Gan, Liyong)[2 ]; Zhang, WY (Zhang, Wenyu)[1 ]; Peng, YC (Peng, Yuecheng)[1 ]; Yu, H (Yu, Hong)[3 ]; Yan, QY (Yan, Qingyu)[3 ]; Xia, XH (Xia, Xinghua)[4 ]; Wang, X (Wang, Xin)[1 ]
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文献类型:Article
摘要
Molecularly well-defined Ni sites at heterogeneous interfaces were derived from the incorporation of Ni2+ ions into heteroatom-doped graphene. The molecular Ni sites on graphene were redox-active. However, they showed poor activity toward oxygen evolution reaction (OER) in KOH aqueous solution. We demonstrated for the first time that the presence of Fe3+ ions in the solution could bond at the vicinity of the Ni sites with a distance of 2.7 angstrom, generating molecularly sized and heterogeneous Ni-Fe sites anchored on doped graphene. These Ni-Fe sites exhibited markedly improved OER activity. The Pourbaix diagram confirmed the formation of the Ni-Fe sites and revealed that the Ni-Fe sites adsorbed HO- ions with a bridge geometry, which facilitated the OER electrocatalysis.
关键词
KeyWords Plus:CATALYTIC WATER OXIDATION; CARBON-MONOXIDE; ARTIFICIAL PHOTOSYNTHESIS; REACTION DYNAMICS; CO2 REDUCTION; REDOX STATES; COMPLEXES; IRON; ELECTRODES; METAL
作者信息
通讯作者地址:Wang, X (通讯作者)
![]() | Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore. |
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电子邮件地址:wangxin@ntu.edu.sg
出版商
类别分类
研究方向:Science & Technology - Other Topics
Web of Science 类别:Multidisciplinary Sciences