Suppr超能文献

一种通用的配体介导的方法,用于大规模合成过渡金属单原子催化剂。

A universal ligand mediated method for large scale synthesis of transition metal single atom catalysts.

机构信息

Key Laboratory of Photochemical Conversion and Optoelectronic Materials Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, 100190, Beijing, China.

Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, 100049, Beijing, China.

出版信息

Nat Commun. 2019 Oct 8;10(1):4585. doi: 10.1038/s41467-019-12510-0.

Abstract

There is interest in metal single atom catalysts due to their remarkable activity and stability. However, the synthesis of metal single atom catalysts remains somewhat ad hoc, with no universal strategy yet reported that allows their generic synthesis. Herein, we report a universal synthetic strategy that allows the synthesis of transition metal single atom catalysts containing Cr, Mn, Fe, Co, Ni, Cu, Zn, Ru, Pt or combinations thereof. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and extended X-ray absorption fine structure spectroscopy confirm that the transition metal atoms are uniformly dispersed over a carbon black support. The introduced synthetic method allows the production of carbon-supported metal single atom catalysts in large quantities (>1 kg scale) with high metal loadings. A Ni single atom catalyst exhibits outstanding activity for electrochemical reduction of carbon dioxide to carbon monoxide, achieving a 98.9% Faradaic efficiency at -1.2 V.

摘要

由于金属单原子催化剂具有显著的活性和稳定性,因此人们对其很感兴趣。然而,金属单原子催化剂的合成仍然有些特别,目前还没有报道一种通用的策略可以允许它们的通用合成。在此,我们报告了一种通用的合成策略,允许合成包含 Cr、Mn、Fe、Co、Ni、Cu、Zn、Ru、Pt 或它们的组合的过渡金属单原子催化剂。像差校正的高角度环形暗场扫描透射电子显微镜和扩展 X 射线吸收精细结构光谱证实,过渡金属原子均匀分散在炭黑载体上。所引入的合成方法允许以高金属负载量(>1kg 规模)大量生产负载在碳上的金属单原子催化剂。Ni 单原子催化剂在电化学还原二氧化碳为一氧化碳方面表现出优异的活性,在-1.2V 时达到 98.9%的法拉第效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/619c/6783464/d00a4ca56054/41467_2019_12510_Fig1_HTML.jpg

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