Room-Temperature Transformation of Bulk Materials into Single Atoms for Advancing CO 2 Electroreduction Efficiency

View at publisher
Authors: Yong Su, Junli Xu, Jia Zhao, Congcong Du, Qiunan Liu, Jiwei Li, Sixu Liu, Zhun Zhang, Yang Luo, Lin Geng, Jingzhao Chen, Kelvin H. L. Zhang
+12 more Yongfu Tang, Liqiang Zhang, Qiao Huang, Kazu Suenaga, Feiteng Wang, Jun Cheng, Sen Lin, Wei Tan, Lin Dong, Fudong Liu, Jianyu Huang, Haifeng Xiong
Cited by: 1
References: 37

Abstract

Metal single-atom catalysts (SACs) offer exceptional atomic efficiency and remarkable properties, making them highly valuable for energy and environmental applications. However, existing SAC preparation methods face challenges, such as the need for high temperatures or limitations in metal loading. In this study, we present a room-temperature synthesis strategy for stable SACs with high metal loadings (>10 wt %), achieved through electrochemical redox reactions within lithium-ion batteries. The reaction mechanism was thoroughly elucidated, revealing that bulk metallic compounds (denoted as M a X b, where M represents a metal and X is F, S, or O) disintegrate from the millimeter scale down to single atoms at room temperature. This process is driven by lithiation–delithiation-induced grain refinement and the dissolution of metals, which are subsequently captured by the substrate. The resulting single-atom catalyst (e.g., Cu SAC) demonstrates outstanding reactivity for electrocatalytic CO 2 reduction, showcasing excellent electrochemical stability and superior performance. This room-temperature redox method is versatile and compatible with a wide range of metals and supports, highlighting its potential for broad applications in sustainable catalytic technologies.

Fields of Study & Subjects

CO2 Reduction Techniques and Catalysts Electrocatalysts for Energy Conversion Catalysts for Methane Reforming

Publication details

Journal / source
ACS Nano
Publisher
American Chemical Society (ACS)
Volume
20
Issue
2
Pages
2248–2257
Publication date
5 January 2026
Language
EN