Stress Dissipation Driven by Multi-Interface Built-In Electric Fields and Desert-Rose-Like Structure for Ultrafast and Superior Long-Term Sodium Ion Storage

被引:11
作者
Li, Jinhang [1 ]
Yu, Huiying [2 ]
Zhao, Yingying [1 ,2 ]
Zhu, Kai [2 ]
Zhu, Chunling [2 ]
Ren, Jing [1 ]
Chou, Shulei [3 ]
Chen, Yujin [1 ,2 ]
机构
[1] Harbin Engn Univ, Coll Phys & Optoelect Engn, Key Lab In Fiber Integrated Opt, Minist Educ, Harbin 150001, Peoples R China
[2] Harbin Engn Univ, Coll Mat Sci & Chem Engn, Key Lab Superlight Mat & Surface Technol, Minist Educ, Harbin 150001, Peoples R China
[3] Wenzhou Univ, Inst Carbon Neutralizat, Coll Chem & Mat Engn, Wenzhou 325035, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Sodium Ion Storage; Stress Dissipation; Architected Structure; Multi-Interface Heterostructure; Na+ Diffusion Regulation; MOS2; NANOSHEETS; PERFORMANCE;
D O I
10.1002/anie.202318000
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The kinetics and durability of conversion-based anodes greatly depend on the intrinsic stress regulating ability of the electrode materials, which has been significantly neglected. Herein, a stress dissipation strategy driven by multi-interface built-in electric fields (BEFs) and architected structure, is innovatively proposed to design ultrafast and long-term sodium ion storage anodes. Binary Mo/Fe sulfide heterostructured nanorods with multi-interface BEFs and staggered cantilever configuration are fabricated to prove our concept. Multi-physics simulations and experimental results confirm that the inner stress in multiple directions can be dissipated by the multi-interface BEFs at the micro-scale, and by the staggered cantilever structure at the macro-scale, respectively. As a result, our designed heterostructured nanorods anode exhibits superb rate capability (332.8 mAh g(-1) at 10.0 A g(-1)) and durable cyclic stability over 900 cycles at 5.0 A g(-1), outperforming other metal chalcogenides. This proposed stress dissipation strategy offers a new insight for developing stable structures for conversion-based anodes.
引用
收藏
页数:10
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