催化作用
对偶(语法数字)
电池(电)
材料科学
纳米技术
化学工程
化学
物理
工程类
热力学
生物化学
文学类
艺术
功率(物理)
作者
Xiaoying Song,Min Wang,Zehui Zhang,Qiushi Yao,Songke Mao,Wei Wang,Shijie Yang,Xilei Ding,Guangbin Zhang,Zhengyi Wang,Changshun Wang,Ziwen Kong,Jing Wu,Linglong Zhang,Yi Huang,Hucheng Song
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2025-06-23
卷期号:18 (9): 94907704-94907704
被引量:3
标识
DOI:10.26599/nr.2025.94907704
摘要
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 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
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