共价键
催化作用
结晶度
电化学
金属
化学工程
盐(化学)
聚合物
材料科学
纳米纤维
化学
纳米技术
高分子化学
有机化学
电极
物理化学
冶金
复合材料
工程类
作者
Kyung Seob Song,Patrick Fritz,Daniel F. Abbott,Lok Nga Poon,Cristiano M. Caridade,Felipe Gándara,Victor Mougel,Ali Coşkun
标识
DOI:10.1002/anie.202309775
摘要
Phthalocyanines (PCs) are intriguing building blocks owing to their stability, physicochemical and catalytic properties. Although PC-based polymers have been reported before, many suffer from relatively low stability, crystallinity, and low surface areas. Utilizing a mixed-metal salt ionothermal approach, we report the synthesis of a series of metallophthalocyanine-based covalent organic frameworks (COFs) starting from 1,2,4,5-tetracyanobenzene and 2,3,6,7-tetracyanoanthracene to form the corresponding COFs named M-pPPCs and M-anPPCs, respectively. The obtained COFs followed the Irving-Williams series in their metal contents, surface areas, and pore volume and featured excellent CO2 uptake capacities up to 7.6 mmol g-1 at 273 K, 1.1 bar. We also investigated the growth of the Co-pPPC and Co-anPPC on a highly conductive carbon nanofiber and demonstrated their high catalytic activity in the electrochemical CO2 reduction, which showed Faradaic efficiencies towards CO up to 74 % at -0.64 V vs. RHE.
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