论文成果
Robust bond linkage between boron-based coating layer and lithium polyacrylic acid binder enables ultra-stable micro-sized germanium anodes
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关键字:SOLID-ELECTROLYTE INTERPHASES; ION BATTERIES; PERFORMANCE; CAPACITY; CARBON; NANOSTRUCTURES; PARTICLES; SILICON; STORAGE; DESIGN
摘要:Micro-sized alloy type germanium (Ge) anodes possess appealing properties for next-generation lithium ions batteries, such as desirable capacity, easy accessibility and greater tap density. Nevertheless, volume expansion accompanied by severe pulverization and continuous growth of solid electrolyte interlayer (SEI) still represent fundamental obstacles to their practical applications. Herein, we propose a fresh strategy of constructing robust bond linkage between boron-based coating layer and lithiated polyacrylic acid (PAALi) binder to circumvent the pulverization problems of Ge anodes. Facile pyrolysis of boric acid can introduce an amorphous boron oxide interphase on Ge microparticles (noted as Ge@B2O3). Then in situ crosslinking reaction between B2O3 and PAALi via B-O-C bond linkage constructs a robust Ge anode (Ge@B-PAALi), which is proved by FTIR and Raman characterizations. Post morphological and compositional investigations reveal the minimized pulverization and a thinner SEI composition. The robust bond linkage strategy endows Ge anode with ultra-stable cycling properties of 1053.8 mAh/g after 500 cycles at 1 A/g vs. 500.7 mAh/g for Ge@PAALi and 372.7 mAh/g for Ge@B2O3, respectively. The proposed bond linkage strategy via artificial coating layer and functional binders unlocks huge potential of alloys and other anodes for next-generation battery applications.
卷号:654
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周震芳

硕士生导师

教师拼音名称:zhouzhenfang

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学历:博士研究生

学位:工学博士

毕业院校:上海大学

所属院系:材料科学与工程学院

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