电催化剂
催化作用
钴
碳纳米管
析氧
水溶液
材料科学
分解水
电子转移
吸附
化学工程
碳纤维
共价键
化学
氢
纳米技术
电化学
电极
无机化学
光化学
有机化学
物理化学
复合材料
工程类
复合数
光催化
作者
Xialiang Li,Haitao Lei,Jieyu Liu,Xuechao Zhao,Shuping Ding,Zongyao Zhang,Xixi Tao,Wei Zhang,Weichao Wang,Xiaohong Zheng,Rui Cao
标识
DOI:10.1002/anie.201807996
摘要
Water splitting is promising to realize a hydrogen-based society. The practical use of molecular water-splitting catalysts relies on their integration onto electrode materials. We describe herein the immobilization of cobalt corroles on carbon nanotubes (CNTs) by four strategies and compare the performance of the resulting hybrids for H2 and O2 evolution. Co corroles can be covalently attached to CNTs with short conjugated linkers (the hybrid is denoted as H1) or with long alkane chains (H2), or can be grafted to CNTs via strong π-π interactions (H3) or via simple adsorption (H4). An activity trend H1≫H3>H2≈H4 is obtained for H2 and O2 evolution, showing the critical role of electron transfer ability on electrocatalysis. Notably, H1 is the first Janus catalyst for both H2 and O2 evolution reactions in pH 0-14 aqueous solutions. Therefore, this work is significant to show potential uses of electrode materials with well-designed molecular catalysts in electrocatalysis.
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