Multiscale Micro‐Nano Hierarchical Porous Germanium with Self‐Adaptive Stress Dispersion for Highly Robust Lithium‐Ion Batteries Anode

Author:

Guo Siguang1,Sun Zhefei2,Liu Yu1,Guo Xinbo1,Feng Haoqin13,Luo Shi1,Wei Changhao1,Zheng Yang1,Zhang Xuming1,Kim Kangwoon4,Liu Haodong4,Chu Paul K5,Gao Biao1ORCID,Zhang Qiaobao2ORCID,Huo Kaifu3

Affiliation:

1. The State Key Laboratory of Refractories and Metallurgy Institute of Advanced Materials and Nanotechnology Wuhan University of Science and Technology Wuhan 430081 China

2. State Key Laboratory of Physical Chemistry of Solid Surfaces College of Materials Xiamen University Xiamen 361005 China

3. Wuhan National Laboratory for Optoelectronics (WNLO) School of Optical and Electronic Information Huazhong University of Science and Technology Wuhan 430074 China

4. Center for Memory and Recording Research Building UC San Diego CA 92093 USA

5. Department of Physics Department of Materials Science and Engineering, and Department of Biomedical Engineering City University of Hong Kong Tat Chee Avenue Kowloon Hong Kong 518057 China

Abstract

AbstractThe manipulation of stress in high‐capacity microscale alloying anode materials, which undergo significant volumetric variation during cycling, is crucial prerequisite for improved their cycling capability. In this work, an innovative structural design strategy is proposed for scalable fabrication of a unique 3D highly porous micro structured germanium (Ge) featuring micro‐nano hierarchical architecture as viable anode for high‐performance lithium‐ion batteries (LIBs). The resultant micro‐sized Ge, consisting of interconnected nanoligaments and bicontinuous nanopores, is endowed with high activity, decreased Li+ diffusion distance and alleviated volume variation, appealing as an ideal platform for in‐depth understanding the relationship between structural design and stress evolution. Such a micro‐sized Ge being highly porous delivers a record high initial Coulombic efficiency of 92.5%, large volumetric capacity of 2,421 mAh cm−3 at 1.2 mA cm−2, exceptional rate capability (805.6 mAh g−1 at 10 Ag−1) and cycling stability (over 90% capacity retention after 1000 cycles even at 5 A g−1), largely outperforming the reported Ge‐based anodes for LIBs. Furthermore, its underlying Li storage mechanism and stress dispersion behavior are explicitly revealed by combined substantial in situ/ex situ experimental characterizations and theoretical computation. This work provides novel insights into the rational design of high‐performance and durable alloying anodes toward high‐energy LIBs.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Shenzhen Knowledge Innovation Program

Publisher

Wiley

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