AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (20.1 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article | Open Access

A long cycle lifespan and high energy efficiency Li–CO2 battery enabled by dual-active site AuRu catalysts on TiO2

Xiaoying Song1,§Min Wang3,§( )Zehui Zhang2Qiushi Yao2Songke Mao4Wei Wang1Shijie Yang2Xilei Ding2Guangbin Zhang2Zhengyi Wang1Changshun Wang2Ziwen Kong1Jing Wu2Linglong Zhang2Yi Huang1( )Hucheng Song2( )
School of Integrated Circuits, Chongqing University of Posts and Telecommunications, Chongqing 400065, China
School of Physics, Nanjing University of Aeronautics and Astronautics, Nanjing 210093, China
National Laboratory of Solid State Microstructures, School of Electronics Science and Engineering, Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093, China
Zhejiang GBS Energy Co., Ltd., Yuyao 315400, China

§ Xiaoying Song and Min Wang contributed equally to this work.

Show Author Information

Abstract

Lithium–carbon dioxide (Li–CO2) batteries have attracted considerable attention due to their high theoretical energy densities and potential for capturing and converting CO2 toward net-zero carbon dioxide emissions. However, the reversible cycling capability of Li–CO2 batteries is greatly limited by the sluggish kinetics of the CO2 evolution reaction (CO2ER), which leads to excessive charge voltages exceeding 4.0 V, thus significantly hindering the practical advancement of the battery technology. Herein, we report dual-active-site AuRu catalysts supported on TiO2 nanorod arrays, grown on carbon nanofiber, where TiO2 layers effectively prevent carbon corrosion and the electronic synergy of the dual active site design comprising Au and Ru can lower the reaction energy barriers of the CO2 reduction reaction (CO2RR) and CO2ER. Calculation results reveal that this synergy gives rise to complementary catalytic roles: Au facilitates CO2 activation, whereas Ru promotes Li2CO3 breakdown, collectively enhancing the overall reaction kinetics. Consequently, Li–CO2 batteries employing AuRu/TiO2 cathode deliver an ultralong cycle life exceeding 1100 cycles (~ 2200 h), low charge voltages (2.9–3.1 V), high energy efficiency (~ 77.9%), and excellent stability at elevated temperatures. This work establishes a generalizable catalyst-support strategy for long lifespan metal–CO2 batteries, offering a promising route toward high-performance carbon neutral energy storage devices.

Graphical Abstract

Dual-active-site AuRu catalysts supported on TiO2 nanorod arrays grown on carbon nanofibers enable Li–CO2 batteries to operate for over 1100 cycles (~ 2200 h) with low charge voltages of 2.9–3.1 V. The catalyst design enhances CO2 activation and Li2CO3 decomposition while stabilizing the carbon framework under high-voltage cycling.

Electronic Supplementary Material

Download File(s)
7704_ESM.pdf (1.1 MB)

References

【1】
【1】
 
 
Nano Research
Article number: 94907704

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Close
Close
Cite this article:
Song X, Wang M, Zhang Z, et al. A long cycle lifespan and high energy efficiency Li–CO2 battery enabled by dual-active site AuRu catalysts on TiO2. Nano Research, 2025, 18(9): 94907704. https://doi.org/10.26599/NR.2025.94907704
Topics:

1690

Views

239

Downloads

3

Crossref

2

Web of Science

2

Scopus

0

CSCD

Received: 02 May 2025
Revised: 11 June 2025
Accepted: 16 June 2025
Published: 27 August 2025
© The Author(s) 2025. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).