共价键
材料科学
卟啉
钴
催化作用
金属
纳米技术
氨
相(物质)
电催化剂
化学气相沉积
组合化学
电极
无机化学
化学工程
有机化学
电化学
化学
物理化学
冶金
工程类
作者
Syed Ibrahim Gnani Peer Mohamed,Shahriar Namvar,Tan Zhang,Hessam Shahbazi,Zhen Jiang,Andrew M. Rappe,Amin Salehi‐Khojin,Siamak Nejati
标识
DOI:10.1002/adma.202309302
摘要
Abstract The inability to process many covalent organic frameworks (COFs) as thin films plagues their widespread utilization. Herein, a vapor‐phase pathway for the bottom‐up synthesis of a class of porphyrin‐based COFs is presented. This approach allows integrating electrocatalysts made of metal‐ion‐containing COFs into the electrodes’ architectures in a single‐step synthesis and deposition. By precisely controlling the metal sites at the atomic level, remarkable electrocatalytic performance is achieved, resulting in unprecedentedly high mass activity values. How the choice of metal atoms, i.e., cobalt and copper, can determine the catalytic activities of POR‐COFs is demonstrated. The theoretical data proves that the Cu site is highly active for nitrate conversion to ammonia on the synthesized COFs.
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