| Literature DB >> 34240536 |
Shengwei Li1, Yongchang Liu1,2, Xudong Zhao1, Kaixuan Cui1, Qiuyu Shen1, Ping Li1, Xuanhui Qu1, Lifang Jiao2.
Abstract
Aqueous Zn-storage behaviors of MoS2 -based cathodes mainly rely on the ion-(de)intercalation at edge sites but are limited by the inactive basal plane. Herein, an in-situ molecular engineering strategy in terms of structure defects manufacturing and O-doping is proposed for MoS2 (designated as D-MoS2 -O) to unlock the inert basal plane, expand the interlayer spacing (from 6.2 to 9.6 Å), and produce abundant 1T-phase. The tailored D-MoS2 -O with excellent hydrophilicity and high conductivity allows the 3D Zn2+ transport along both the ab plane and c-axis, thus achieving the exceptional high rate capability. Zn2+ diffusion through the basal plane is verified by DFT computations. As a proof of concept, the wearable quasi-solid-state rechargeable Zn battery employing the D-MoS2 -O cathode operates stably even under severe bending conditions, showing great application prospects. This work opens a new window for designing high-performance layered cathode materials for aqueous Zn-ion batteries.Entities:
Keywords: DFT computations; MoS2; aqueous Zn-ion batteries; cathode materials; molecular engineering
Year: 2021 PMID: 34240536 DOI: 10.1002/anie.202108317
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336