TY - JOUR
T1 - Unravelling asynchronous oxidation of carbon and lithium carbonate during charging in lithium-carbon dioxide battery
AU - Li, Wanzhen
AU - Wang, Wentao
AU - Zhu, Ningxuan
AU - Tan, Chuan
AU - Gao, Xiangwen
AU - Chen, Yuhui
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/6/1
Y1 - 2025/6/1
N2 - Lithium carbonate (Li2CO3) and carbon (C) play crucial roles as primary discharge products in lithium-carbon dioxide (Li-CO2) batteries. Understanding the reversible formation and oxidation of Li2CO3 and C during charge-discharge cycles is essential for the cyclic performance of Li-CO2 batteries. However, the role of the decomposition mechanisms of Li2CO3 and the C substrate remains debated, especially under real operating conditions. Here, we find that the discharge product C undergoes oxidation during charging, displaying non-synchronous oxidation compared to Li2CO3. Oxidation primarily involves C and the electrolyte in the early charging stages, producing CO2 and CO. In the later stages, the decomposition of Li2CO3 predominates, producing highly reactive CO3·- intermediates. Interestingly, after prolonged ball milling of lithium carbonate and carbon, the C elements can be exchanged through Li2CO3•C composite materials. By forming Li2CO3•C composites, C can be oxidized synchronously during the charging. Therefore, designing a catalyst to promote the reversible formation/decomposition of Li2CO3•C could be vital to achieving reversible cycling in Li-CO2 batteries.
AB - Lithium carbonate (Li2CO3) and carbon (C) play crucial roles as primary discharge products in lithium-carbon dioxide (Li-CO2) batteries. Understanding the reversible formation and oxidation of Li2CO3 and C during charge-discharge cycles is essential for the cyclic performance of Li-CO2 batteries. However, the role of the decomposition mechanisms of Li2CO3 and the C substrate remains debated, especially under real operating conditions. Here, we find that the discharge product C undergoes oxidation during charging, displaying non-synchronous oxidation compared to Li2CO3. Oxidation primarily involves C and the electrolyte in the early charging stages, producing CO2 and CO. In the later stages, the decomposition of Li2CO3 predominates, producing highly reactive CO3·- intermediates. Interestingly, after prolonged ball milling of lithium carbonate and carbon, the C elements can be exchanged through Li2CO3•C composite materials. By forming Li2CO3•C composites, C can be oxidized synchronously during the charging. Therefore, designing a catalyst to promote the reversible formation/decomposition of Li2CO3•C could be vital to achieving reversible cycling in Li-CO2 batteries.
KW - CO isotope labeled
KW - CO
KW - Li-CO battery
KW - LiCO decomposition
UR - http://www.scopus.com/inward/record.url?scp=86000741233&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2025.236737
DO - 10.1016/j.jpowsour.2025.236737
M3 - 文章
AN - SCOPUS:86000741233
SN - 0378-7753
VL - 640
JO - Journal of Power Sources
JF - Journal of Power Sources
M1 - 236737
ER -