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胺功能化无金属纳米碳促进流动池中一氧化碳选择性电还原为一氧化碳

Amine-Functionalized Metal-Free Nanocarbon to Boost Selective CO Electroreduction to CO in a Flow Cell.

作者信息

An Guangbin, Wang Kang, Wang Zeming, Zhang Mingwan, Guo Huazhang, Wang Liang

机构信息

Institute of Nanochemistry and Nanobiology, School of Environmental and Chemical Engineering, Shanghai University, 99 Shangda Road, BaoShan District, Shanghai 200444, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2024 Jun 5;16(22):29060-29068. doi: 10.1021/acsami.4c04502. Epub 2024 May 20.

Abstract

Highly efficient electrochemical CO-to-CO conversion is a promising approach for achieving carbon neutrality. While nonmetallic carbon electrocatalysts have shown potential for CO-to-CO utilization in H-type cells, achieving efficient conversion in flow cells at an industrial scale remains challenging. In this study, we present a cost-effective synthesis strategy for preparing ultrathin 2D carbon nanosheet catalysts through simple amine functionalization. The optimized catalyst, NCNs-2.5, demonstrates exceptional CO selectivity with a maximum Faradaic efficiency of 98% and achieves a high current density of 55 mA cm in a flow cell. Furthermore, the catalyst exhibits excellent long-term stability, operating continuously for 50 h while maintaining a CO selectivity above 90%. The superior catalytic activity of NCNs-2.5 is attributed to the presence of amine-N active sites within the carbon lattice structure. This work establishes a foundation for the rational design of cost-effective nonmetallic carbon catalysts as sustainable alternatives to metals in energy conversion systems.

摘要

高效电化学CO转化为CO是实现碳中和的一种很有前景的方法。虽然非金属碳电催化剂在H型电池中已显示出CO转化利用的潜力,但在工业规模的流动电池中实现高效转化仍具有挑战性。在本研究中,我们提出了一种经济高效的合成策略,通过简单的胺功能化制备超薄二维碳纳米片催化剂。优化后的催化剂NCNs-2.5表现出优异的CO选择性,最大法拉第效率为98%,并在流动电池中实现了55 mA cm的高电流密度。此外,该催化剂表现出优异的长期稳定性,连续运行50小时,同时保持CO选择性高于90%。NCNs-2.5的优异催化活性归因于碳晶格结构中胺-N活性位点的存在。这项工作为合理设计经济高效的非金属碳催化剂奠定了基础,作为能量转换系统中金属的可持续替代品。

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