Robust bond linkage between boron-based coating layer and lithium polyacrylic acid binder enables ultra-stable micro-sized germanium anodes

Key Words:SOLID-ELECTROLYTE INTERPHASES; ION BATTERIES; PERFORMANCE; CAPACITY; CARBON; NANOSTRUCTURES; PARTICLES; SILICON; STORAGE; DESIGN

Abstract: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.

Volume:654

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Translation or Not:no