Evolution of the electrochemical interface in sodium ion batteries with ether electrolytes

Kaikai Li(Hong Kong Polytechnic University), Jun Zhang(Tsinghua–Berkeley Shenzhen Institute), Dongmei Lin(Hong Kong Polytechnic University), Dawei Wang(UNSW Sydney), Baohua Li(Tsinghua University), Wei Lv(Tsinghua University), Sheng Sun(Shanghai University), Yan‐Bing He(Tsinghua University), Feiyu Kang(Tsinghua–Berkeley Shenzhen Institute), Quan‐Hong Yang(Tianjin University), Limin Zhou(Hong Kong Polytechnic University), Tong‐Yi Zhang(Shanghai University)
Nature Communications
February 13, 2019
Cited by 473Open Access
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Abstract

Ether based electrolytes have surfaced as alternatives to conventional carbonates allowing for enhanced electrochemical performance of sodium-ion batteries; however, the primary source of the improvement remains poorly understood. Here we show that coupling titanium dioxide and other anode materials with diglyme does enable higher efficiency and reversible capacity than those for the combination involving ester electrolytes. Importantly, the electrolyte dependent performance is revealed to be the result of the different structural evolution induced by a varied sodiation depth. A suit of characterizations show that the energy barrier to charge transfer at the interface between electrolyte and electrode is the factor that dominates the interfacial electrochemical characteristics and therefore the energy storage properties. Our study proposes a reliable parameter to assess the intricate sodiation dynamics in sodium-ion batteries and could guide the design of aprotic electrolytes for next generation rechargeable batteries.


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