Suppr超能文献

用于安培级电流下CO电还原的基于MOF的单原子镍催化剂的微波辅助快速合成

Microwave-Assisted Rapid Synthesis of MOF-Based Single-Atom Ni Catalyst for CO Electroreduction at Ampere-Level Current.

作者信息

Wen Ming, Sun Nana, Jiao Long, Zang Shuang-Quan, Jiang Hai-Long

机构信息

Henan Key Laboratory of Crystalline Molecular Functional Materials, Henan International Joint Laboratory of Tumor Theranostical Cluster Materials, Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, P. R. China.

Hefei National Research Center for Physical Sciences at the Microscale, Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2024 Mar 4;63(10):e202318338. doi: 10.1002/anie.202318338. Epub 2024 Jan 30.

Abstract

Carbon-based single-atom catalysts (SACs) have attracted tremendous interest in heterogeneous catalysis. However, the common electric heating techniques to produce carbon-based SACs usually suffer from prolonged heating time and tedious operations. Herein, a general and facile microwave-assisted rapid pyrolysis method is developed to afford carbon-based SACs within 3 min without inert gas protection. The obtained carbon-based SACs present high porosity and comparable carbonization degree to those obtained by electric heating techniques. Specifically, the single-atom Ni implanted N-doped carbon (Ni -N-C) derived from a Ni-doped metal-organic framework (Ni-ZIF-8) exhibits remarkable CO Faradaic efficiency (96 %) with a substantial CO partial current density (j ) up to 1.06 A/cm in CO electroreduction, far superior to the counterpart obtained by traditional pyrolysis with electric heating. Mechanism investigations reveal that the resulting Ni -N-C presents abundant defective sites and mesoporous structure, greatly facilitating CO adsorption and mass transfer. This work establishes a versatile approach to rapid and large-scale synthesis of SACs as well as other carbon-based materials for efficient catalysis.

摘要

碳基单原子催化剂(SACs)在多相催化领域引起了广泛关注。然而,制备碳基SACs的常用电加热技术通常存在加热时间长和操作繁琐的问题。在此,我们开发了一种通用且简便的微波辅助快速热解方法,无需惰性气体保护,即可在3分钟内制备出碳基SACs。所制备的碳基SACs具有高孔隙率,且碳化程度与通过电加热技术获得的相当。具体而言,由镍掺杂金属有机框架(Ni-ZIF-8)衍生而来的单原子镍植入氮掺杂碳(Ni-N-C)在CO电还原中表现出显著的CO法拉第效率(96%),其CO分电流密度(j)高达1.06 A/cm²,远优于传统电加热热解制备的同类催化剂。机理研究表明,所得的Ni-N-C具有丰富的缺陷位点和介孔结构,极大地促进了CO的吸附和传质。这项工作建立了一种通用方法,可快速大规模合成SACs以及其他用于高效催化的碳基材料。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验