阴极
材料科学
超晶格
插层(化学)
阳极
电极
上部结构
同步加速器
电解质
化学工程
纳米技术
光电子学
无机化学
化学
热力学
光学
物理
工程类
物理化学
作者
Zeying Yao,Wei Zhang,Xiaochuan Ren,Yaru Yin,Yuanxin Zhao,Zhiguo Ren,Yuanhe Sun,Qi Lei,Juan Wang,Lihua Wang,Te Ji,Ping Huai,Wen Wen,Xiaolong Li,Daming Zhu,Renzhong Tai
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-08-01
卷期号:16 (8): 12095-12106
被引量:97
标识
DOI:10.1021/acsnano.2c02330
摘要
Engineering multifunctional superstructure cathodes to conquer the critical issue of sluggish kinetics and large volume changes associated with divalent Zn-ion intercalation reactions is highly desirable for boosting practical Zn-ion battery applications. Herein, it is demonstrated that a MoS2/C19H42N+ (CTAB) superstructure can be rationally designed as a stable and high-rate cathode. Incorporation of soft organic CTAB into a rigid MoS2 host forming the superlattice structure not only effectively initiates and smooths Zn2+ transport paths by significantly expanding the MoS2 interlayer spacing (1.0 nm) but also endows structural stability to accommodate Zn2+ storage with expansion along the MoS2 in-plane, while synchronous shrinkage along the superlattice interlayer achieves volume self-regulation of the whole cathode, as evidenced by in situ synchrotron X-ray diffraction and substantial ex situ characterizations. Consequently, the optimized superlattice cathode delivers high-rate performance, long-term cycling stability (∼92.8% capacity retention at 10 A g-1 after 2100 cycles), and favorable flexibility in a pouch cell. Moreover, a decent areal capacity (0.87 mAh cm-2) is achieved even after a 10-fold increase of loading mass (∼11.5 mg cm-2), which is of great significance for practical applications. This work highlights the design of multifunctional superlattice electrodes for high-performance aqueous batteries.
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