{"title":"Catalytic Promotion of Transition-Metal-Doped Graphene Cathodes in Li-CO2 Batteries","authors":"Peter P. Bazianos, Zhen Jiang, Andrew M. Rappe","doi":"10.1021/acs.jpcc.4c06763","DOIUrl":null,"url":null,"abstract":"The Li-CO<sub>2</sub> battery is a promising energy storage system with impressive theoretical specific energy and discharge capacity. Graphene-based single-atom catalysts (SACs) provide high surface area and long-term electrochemical reactivity and stability, making SACs among the most promising cathode catalysts for these batteries. However, current Li-CO<sub>2</sub> systems have high reaction barriers, slowing the reaction and greatly increasing the overpotential. Improvement of the discharge/charge energetics requires atomic-level innovations in cathode design, such as alterations to the catalyst chemical structure. In this paper, we propose enhancing the SAC by using a Ti metal center, which is found to deliver the highest electrochemical Li + CO<sub>2</sub> activity among 3d transition metal candidates. Furthermore, we propose cathode surface coating with ionic liquids, since these environments promote the formation of reaction intermediates in the electrochemical conversion process. Our work provides insights to optimize electrode design for high-performance Li-CO<sub>2</sub> batteries, which can open new avenues to recycle greenhouse gases and achieve enhanced renewable energy storage.","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"43 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpcc.4c06763","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
锂-二氧化碳电池是一种前景广阔的储能系统,其理论比能量和放电容量令人印象深刻。基于石墨烯的单原子催化剂(SAC)具有高表面积、长期电化学反应活性和稳定性,使其成为这类电池最有前途的阴极催化剂之一。然而,目前的锂-CO2 系统具有较高的反应壁垒,减缓了反应速度并大大增加了过电位。改善放电/充电能量需要在阴极设计方面进行原子级创新,例如改变催化剂的化学结构。在本文中,我们建议通过使用 Ti 金属中心来增强 SAC,发现在 3d 过渡金属候选物质中,Ti 金属中心具有最高的 Li + CO2 电化学活性。此外,我们还建议在阴极表面涂覆离子液体,因为这些环境会促进电化学转换过程中反应中间产物的形成。我们的工作为优化高性能锂-CO2 电池的电极设计提供了见解,从而为回收温室气体和实现增强型可再生能源存储开辟了新途径。
Catalytic Promotion of Transition-Metal-Doped Graphene Cathodes in Li-CO2 Batteries
The Li-CO2 battery is a promising energy storage system with impressive theoretical specific energy and discharge capacity. Graphene-based single-atom catalysts (SACs) provide high surface area and long-term electrochemical reactivity and stability, making SACs among the most promising cathode catalysts for these batteries. However, current Li-CO2 systems have high reaction barriers, slowing the reaction and greatly increasing the overpotential. Improvement of the discharge/charge energetics requires atomic-level innovations in cathode design, such as alterations to the catalyst chemical structure. In this paper, we propose enhancing the SAC by using a Ti metal center, which is found to deliver the highest electrochemical Li + CO2 activity among 3d transition metal candidates. Furthermore, we propose cathode surface coating with ionic liquids, since these environments promote the formation of reaction intermediates in the electrochemical conversion process. Our work provides insights to optimize electrode design for high-performance Li-CO2 batteries, which can open new avenues to recycle greenhouse gases and achieve enhanced renewable energy storage.
期刊介绍:
The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.