催化作用
儿茶酚
钌
氢
碳纤维
聚合物
材料科学
化学工程
化学
无机化学
高分子化学
有机化学
复合数
工程类
复合材料
作者
Tong Wu,Jing Hong,Zhenwu Lu,Haiyang Wu,Chenzhi Wu,Zhenbin Tang,Xiaohui Liu,Birong Zeng,Yiting Xu,Guorong Chen,Conghui Yuan,Lizong Dai
标识
DOI:10.1016/j.apcatb.2020.119795
摘要
We report a coordinative strategy to introduce ruthenium (Ru) into nitrogen, boron co-doped carbon nanomaterials (Ru-NBCs) thus achieving high hydrogen evolution reaction (HER) activity in both alkaline and acidic conditions. Starting from boronate polymer nanospheres prepared by a condensation reaction between catechol and boronic monomers, a Ru3+-catechol coordination reaction can easily produce metallosupramolecular polymer precursors. Ru-NBCs derived from the sintering of these precursors exhibit excellent HER properties with lowest overpotentials of 14 mV in 1.0 M KOH and 22 mV in 0.5 M H2SO4 at a current density of 10 mA/cm2. The mass activity of Ru-NBCs is much higher than that of commercial Pt/C. Meanwhile, the active site density and turnover frequency (TOF) value of Ru-NBCs are studied. This strategy has high adaptability to various catechol and boronic building blocks with different structures, thus showing promising application in the design of high performance metal-incorporated doped carbon materials.
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