DUBOIS, Vincent; PECQUENARD, Brigitte; SOULÉ, Samantha; MARTINEZ, Hervé; LE CRAS, Frédéric

doi:10.1021/acsami.6b11987

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DUBOIS, Vincent
STMicroelectronics
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]

PECQUENARD, Brigitte
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]

SOULÉ, Samantha
Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux [IPREM]

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Ce document a été publié dans

ACS Applied Materials & Interfaces. 2017, vol. 9, n° 3, p. 2275-2284

Washington, D.C. : American Chemical Society

Résumé en anglais

A dual redox process involving Ti3+/Ti4+ cation species and S2–/(S2)2– anion species is highlighted in oxygenated lithium titanium sulfide thin film electrodes during lithium (de)insertion, leading to a high specific capacity. These cathodes for all-solid-state lithium-ion microbatteries are synthesized by sputtering of LiTiS2 targets prepared by different means. The limited oxygenation of the films that is induced during the sputtering process favors the occurrence of the S2–/(S2)2– redox process at the expense of the Ti3+/Ti4+ one during the battery operation, and influences its voltage profile. Finally, a perfect reversibility of both electrochemical processes is observed, whatever the initial film composition. All-solid-state lithium microbatteries using these amorphous lithiated titanium disulfide thin films and operated between 1.5 and 3.0 V/Li+/Li deliver a greater capacity (210–270 mAh g–1) than LiCoO2, with a perfect capacity retention (−0.0015% cycle–1).< Réduire

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disulfide pairs

titanium sulfide

thin films

all-solid-state lithium batteries

LiTiS 2

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Dual cation- and anion-based redox process in lithium titanium oxysulfide thin film cathodes

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