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Michel Armand

Researcher at Deakin University

Publications -  49
Citations -  2889

Michel Armand is an academic researcher from Deakin University. The author has contributed to research in topics: Electrolyte & Lithium. The author has an hindex of 26, co-authored 49 publications receiving 1798 citations. Previous affiliations of Michel Armand include Cooperative Research Centre.

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Ultrahigh Performance All Solid-State Lithium Sulfur Batteries: Salt Anion’s Chemistry-Induced Anomalous Synergistic Effect

TL;DR: An ultrahigh performance of ASSLSBs is obtained via an anomalous synergistic effect between (fluorosulfonyl)(trifluoromethanesulfonyL)imide anions inherited from the design of lithium salts in SPEs and the polysulfide species formed during the cycling, implying the importance of the molecular structure of lithium salt in ASSLSB and paving a way for future development of safe and cost-effective Li-S batteries.
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Lithium Azide as an Electrolyte Additive for All-Solid-State Lithium-Sulfur Batteries.

TL;DR: In this article, LiN3 was used as an electrolyte additive for all-solid-state Li-S batteries to avoid dendrite formation and polysulfide shuttling.
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Polymeric Schiff Bases as Low‐Voltage Redox Centers for Sodium‐Ion Batteries

TL;DR: Electroactive polymeric Schiff bases were produced by reaction between non-conjugated aliphatic or conjugated aromatic diamine block with terephthalaldehyde unit, able to electrochemically store more than one sodium atom per azomethine group.
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Lithium Bis(fluorosulfonyl)imide/Poly(ethylene oxide) Polymer Electrolyte for All Solid-State Li–S Cell

TL;DR: The cycling performances of Li-S polymer cell with LiFSI are significantly improved compared with those with conventional LiTFSI (Li[N(SO2CF3)2]) salt in the polymer membrane due to the improved stability of the Li anode/electrolyte interphases formed in theLiFSI-based SPEs.
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Insight into the Atomic Structure of High-Voltage Spinel LiNi0.5Mn1.5O4 Cathode Material in the First Cycle

TL;DR: In this paper, the average structure of LiNi0.5Mn1.5O4 was investigated during the first cycle (3.5-4.9 V) at room temperature, and two types of local atomic-level migration of transition metals (TM) ions in the cathode were observed.