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Nb1.60Ti0.32W0.08O5−δ as negative electrode active material for durable and fast-charging all-solid-state Li-ion batteries.

Authors :
Kim, Chanho
Nam, Gyutae
Ahn, Yoojin
Hu, Xueyu
Liu, Meilin
Source :
Nature Communications; 10/16/2024, Vol. 15 Issue 1, p1-10, 10p
Publication Year :
2024

Abstract

Li-based all-solid-state batteries (ASSBs) are considered feasible candidates for the development of the next generation of high-energy rechargeable batteries. However, ASSBs are detrimentally affected by a limited rate capability and inadequate performance at high currents. To circumvent these issues, here we propose the use of Nb<subscript>1.60</subscript>Ti<subscript>0.32</subscript>W<subscript>0.08</subscript>O<subscript>5-δ</subscript> (NTWO) as negative electrode active material. NTWO is capable of overcoming the limitation of lithium metal as the negative electrode, offering fast-charging capabilities and cycle stability. Physicochemical and electrochemical characterizations of NTWO in combination with the Li<subscript>6</subscript>PS<subscript>5</subscript>Cl (LPSCl) solid-state electrolyte demonstrate that the formation of LiWS<subscript>2</subscript> at the electrode|electrolyte interphase is the main responsible for the improved battery performance. Indeed, when an NTWO-based negative electrode and LPSCl are coupled with a LiNbO<subscript>3</subscript>-coated LiNi<subscript>0.8</subscript>Mn<subscript>0.1</subscript>Co<subscript>0.1</subscript>O<subscript>2</subscript>-based positive electrode, the lab-scale cell is capable of maintaining 80% of discharge capacity retention after 5000 cycles at 45 mA cm<superscript>−2</superscript> at 60 °C and 60 MPa. All-solid-state batteries (ASSB) are designed to address the limitations of conventional lithium ion batteries. Here, authors developed a Nb1.60Ti0.32W0.08O5-δ negative electrode for ASSBs, which improves fast-charging capability and cycle stability. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
180268989
Full Text :
https://doi.org/10.1038/s41467-024-52767-8