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一种用于水中电催化二氧化碳还原的稳定且导电的金属酞菁骨架

A Stable and Conductive Metallophthalocyanine Framework for Electrocatalytic Carbon Dioxide Reduction in Water.

作者信息

Huang Ning, Lee Ka Hung, Yue Yan, Xu Xiaoyi, Irle Stefan, Jiang Qiuhong, Jiang Donglin

机构信息

Department of Chemistry, Faculty of Science, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore.

MOE Key Laboratory of Macromolecular Synthesis and Functionalization, State Key Laboratory of Silicon Materials, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.

出版信息

Angew Chem Int Ed Engl. 2020 Sep 14;59(38):16587-16593. doi: 10.1002/anie.202005274. Epub 2020 Jul 13.

Abstract

Transformation of carbon dioxide to high value-added chemicals becomes a significant challenge for clean energy studies. Here a stable and conductive covalent organic framework was developed for electrocatalytic carbon dioxide reduction to carbon monoxide in aqueous solution. The cobalt(II) phthalocyanine catalysts are topologically connected via robust phenazine linkage into a two-dimensional tetragonal framework that is stable under boiling water, acid, or base conditions. The 2D lattice enables full π conjugation along x and y directions as well as π conduction along the z axis across the π columns. With these structural features, the electrocatalytic framework exhibits a faradaic efficiency of 96 %, an exceptional turnover number up to 320 000, and a long-term turnover frequency of 11 412 hour , which is a 32-fold improvement over molecular catalyst. The combination of catalytic activity, selectivity, efficiency, and durability is desirable for clean energy production.

摘要

将二氧化碳转化为高附加值化学品已成为清洁能源研究中的一项重大挑战。在此,我们开发了一种稳定且导电的共价有机框架,用于在水溶液中将二氧化碳电催化还原为一氧化碳。钴(II)酞菁催化剂通过坚固的吩嗪键拓扑连接成二维四方框架,该框架在沸水、酸或碱条件下均稳定。二维晶格使得沿x和y方向实现完全的π共轭,以及沿z轴穿过π柱的π传导。凭借这些结构特征,该电催化框架展现出96%的法拉第效率、高达320000的优异周转数以及11412 h⁻¹的长期周转频率,这比分子催化剂提高了32倍。催化活性、选择性、效率和耐久性的结合对于清洁能源生产而言是十分理想的。

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