单宁酸
化学
催化作用
石墨烯
涂层
金属
热解
光催化
纳米技术
Atom(片上系统)
异质结
多孔性
化学工程
材料科学
无机化学
有机化学
光电子学
工程类
嵌入式系统
计算机科学
作者
Haifeng Wang,Xiaopeng Li,Ying Jiang,Minhan Li,Qi Xiao,Tao Zhao,Shuai Yang,Chunhong Qi,Pengpeng Qiu,Jianping Yang,Zheng Jiang,Wei Luo
标识
DOI:10.1002/ange.202200465
摘要
Abstract Here, we report a universal single‐atom coating (SAC) strategy by taking advantage of the rich chemistry of tannic acid (TA). TA units not only self‐assemble into a cross‐linked porous polyphenolic framework, but also can grip on different substates via multiple binding modes. Benefiting from the diverse chelating ability of TA, a series of mono‐, and bi‐metallic SACs can be formed on substrates of different materials (e. g., carbon, SiO 2 , TiO 2 , MoS 2 ), dimensions (0D–3D) and sizes (50 nm–5 cm). By contrast, uniform SAC cannot be achieved using common approaches such as pyrolysis of metal–dopamine complexes or metal–organic frameworks. As a proof‐of‐concept demonstration, two Co SACs immobilized on graphene and TiO 2 were prepared. The former one shows six‐fold higher mass activity than Pt/C toward oxygen reduction. The latter one displays outstanding photocatalytic activity owing to the high activity of the single atoms and the formation of the single‐atom coating–TiO 2 heterojunction.
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