Abstract

Lithium metal batteries (LMBs) and anode‐free LMBs (AFLMBs) present a solution to the need for batteries with a significantly superior theoretical energy density. However, their adoption is hindered by low Coulombic efficiency (CE) and rapid capacity fading, primarily due to the formation of unstable solid electrolyte interphase (SEI) layer and Li dendrite growth as a result of uneven Li plating. Here, we report on the use of a stoichiometric Ti3C2Tx (S‐Ti3C2Tx) MXene coating on the copper current collector to enhance the cyclic stability of an anode‐free lithium metal battery. The S‐Ti3C2Tx coating provides abundant nucleation sites, thereby lowering the overpotential for Li nucleation, and promoting uniform Li plating. Additionally, the fluorine (−F) termination of S‐Ti3C2Tx participates in the SEI formation, producing a LiF‐rich SEI layer, vital for stabilizing the SEI and improving cycle life. Batteries equipped with S‐Ti3C2Tx@Cu current collectors displayed reduced Li consumption during stable SEI formation, resulting in a significant decrease in capacity loss. AFLMBs with S‐Ti3C2Tx@Cu current collectors achieved a high initial capacity density of 4.2 mAh cm−2, 70.9% capacity retention after 50 cycles, and an average CE of 98.19% in 100 cycles. This innovative application of MXenes in the energy field offers a promising strategy to enhance the performance of AFLMBs and could potentially accelerate their commercial adoption.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.