| Literature DB >> 35912958 |
Zeying Yao1,2,3, Wei Zhang1,2,3, Xiaochuan Ren4, Yaru Yin5,6, Yuanxin Zhao1,2, Zhiguo Ren1,2, Yuanhe Sun1,2,3, Qi Lei1,2,3, Juan Wang1,2, Lihua Wang1,2, Te Ji2, Ping Huai5,6, Wen Wen1,2, Xiaolong Li1,2, Daming Zhu1,2, Renzhong Tai1,2.
Abstract
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.Entities:
Keywords: aqueous zinc-ion battery; cathode; self-regulation; superlattice; synchrotron radiation
Year: 2022 PMID: 35912958 DOI: 10.1021/acsnano.2c02330
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 18.027