咪唑酸框架衍生的单原子镍催化剂,用于将CO2还原为CO†

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Yuting Li, Dandan Wang, Yuqin Ma, Fangbin Liu, Hongji Li, Qigming Xu and Haijiao Xie
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引用次数: 0

摘要

利用电化学方法减少二氧化碳(CO2)是实现碳回收的方法之一,因为二氧化碳排放的增加会造成环境问题。单原子分散Ni-NC位催化剂已经成为将CO2还原为CO的有效电催化剂。我们以ZIF-8为载体,通过阐明NiNx位在热活化过程中的结构演变以及其他关键的外部因素,如碳粒度和镍含量,设计出高性能的单镍位催化剂。煅烧后生成的吡啶N活性位点具有较高的活性和CO选择性。该催化剂在−0.88 V时CO生成率高达99.6%,是将CO2还原为CO的最佳催化剂之一。本研究证明了通过调整单原子锚定载流子的表面结构来设计高效的电化学CO2还原催化剂的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An imidazolate framework-derived single-atom nickel catalyst for the reduction of CO2 to CO†

The reduction of carbon dioxide (CO2) using electrochemical methods is one of the ways to achieve carbon recycling, as the increase in carbon dioxide emissions causes environmental problems. Single-atom dispersed Ni-NC site catalysts have emerged as effective electrocatalysts for the reduction of CO2 to CO. Using ZIF-8 as a carrier, we aim to design a high-performance single nickel-site catalyst by elucidating the structure evolution of NiNx sites during thermal activation as well as other key external factors such as the carbon particle size and nickel content. The pyridine N active sites generated after calcination have higher activity and CO selectivity. The catalyst achieved up to 99.6% CO generation at −0.88 V vs. RHE, and is one of the best catalysts for the reduction of CO2 to CO. This work demonstrates an effective method for designing efficient electrochemical CO2 reduction catalysts by tuning the surface structure of single-atom anchored carriers.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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