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Browsing by Author "Xu, Gui-Liang"
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Item Boosting Superior Lithium Storage Performance of Alloy‐Based Anode Materials via Ultraconformal Sb Coating–Derived Favorable Solid‐Electrolyte Interphase(Wiley, 2020-01) Xiong, Bing-Qing; Zhou, Xinwei; Xu, Gui-Liang; Liu, Yuzi; Zhu, Likun; Hu, Youcheng; Shen, Shou-Yu; Hong, Yu-Hao; Wan, Si-Cheng; Liu, Xiao-Chen; Liu, Xiang; Chen, Shengli; Huang, Ling; Sun, Shi-Gang; Amine, Khalil; Ke, Fu-Sheng; Mechanical and Energy Engineering, School of Engineering and TechnologyAlloy materials such as Si and Ge are attractive as high‐capacity anodes for rechargeable batteries, but such anodes undergo severe capacity degradation during discharge–charge processes. Compared to the over‐emphasized efforts on the electrode structure design to mitigate the volume changes, understanding and engineering of the solid‐electrolyte interphase (SEI) are significantly lacking. This work demonstrates that modifying the surface of alloy‐based anode materials by building an ultraconformal layer of Sb can significantly enhance their structural and interfacial stability during cycling. Combined experimental and theoretical studies consistently reveal that the ultraconformal Sb layer is dynamically converted to Li3Sb during cycling, which can selectively adsorb and catalytically decompose electrolyte additives to form a robust, thin, and dense LiF‐dominated SEI, and simultaneously restrain the decomposition of electrolyte solvents. Hence, the Sb‐coated porous Ge electrode delivers much higher initial Coulombic efficiency of 85% and higher reversible capacity of 1046 mAh g−1 after 200 cycles at 500 mA g−1, compared to only 72% and 170 mAh g−1 for bare porous Ge. The present finding has indicated that tailoring surface structures of electrode materials is an appealing approach to construct a robust SEI and achieve long‐term cycling stability for alloy‐based anode materials.Item In Situ Construction of an Ultrarobust and Lithiophilic Li-Enriched Li–N Nanoshield for High-Performance Ge-Based Anode Materials(ACS, 2020-11) Xiong, Bing-Qing; Zhou, Xinwei; Xu, Gui-Liang; Liu, Xiang; Hu, Youcheng; Liu, Yuzi; Zhu, Likun; Shi, Chen-Guang; Hong, Yu-Hao; Wan, Si-Cheng; Sun, Cheng-Jun; Chen, Shengli; Huang, Ling; Sun, Shi-Gang; Amine, Khalil; Ke, Fu-Sheng; Mechanical and Energy Engineering, School of Engineering and TechnologyAlloy-based materials are promising anodes for rechargeable batteries because of their higher theoretical capacities in comparison to graphite. Unfortunately, the huge volume changes during cycling cause serious structural degradation and undesired parasitic reactions with electrolytes, resulting in fragile solid-electrolyte interphase formation and serious capacity decay. This work proposes to mitigate the volume changes and suppress the interfacial reactivity of Ge anodes without sacrificing the interfacial Li+ transport, through in situ construction of an ultrarobust and lithiophilic Li-enriched Li–N nanoshield, which demonstrated improved chemical, electrochemical, mechanical, and environmental stability. Therefore, it can serve as a versatile interlayer to facilitate Li+ transport and effectively block the attack of electrolyte solvents, thus boosting the long-term cycle stability and fast charging capability of Ge anodes. This work offers an alternative methodology to tune the interfaces of other electrode materials as well by screening for more N-containing compounds that can react with Li+ during battery operation.Item A practical phosphorus-based anode material for high-energy lithium-ion batteries(Elsevier, 2020-08) Amine, Rachid; Daali, Amine; Zhou, Xinwei; Liu, Xiang; Liu, Yuzi; Ren, Yang; Zhang, Xiaoyi; Zhu, Likun; Al-Hallaj, Said; Chen, Zonghai; Xu, Gui-Liang; Amine, Khalil; Mechanical and Energy Engineering, School of Engineering and TechnologyState-of-the-art lithium-ion batteries cannot satisfy the increasing energy demand worldwide because of the low specific capacity of the graphite anode. Silicon and phosphorus both show much higher specific capacity; however, their practical use is significantly hindered by their large volume changes during charge/discharge. Although significant efforts have been made to improve their cycle life, the initial coulombic efficiencies of the reported Si-based and P-based anodes are still unsatisfactory (<90%). Here, by using a scalable high-energy ball milling approach, we report a practical hierarchical micro/nanostructured P-based anode material for high-energy lithium-ion batteries, which possesses a high initial coulombic efficiency of 91% and high specific capacity of ~2500 mAh g−1 together with long cycle life and fast charging capability. In situ high-energy X-ray diffraction and in situ single-particle charging/discharging were used to understand its superior lithium storage performance. Moreover, proof-of-concept full-cell lithium-ion batteries using such an anode and a LiNi0.6Co0.2Mn0.2O2 cathode were assembled to show their practical use. The findings presented here can serve as a good guideline for the future design of high-performance anode materials for lithium-ion batteries.