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Pseudocapacitive Na-Ion Storage Boosts High Rate and Areal Capacity of Self-Branched 2D Layered Metal Chalcogenide Nanoarrays

Dongliang ChaoSchool of Physical and Mathematical Sciences, Nanyang Technological University, 637371, SingaporePei LiangCollege of Optical and Electronic Technology, China Jiliang University, Hangzhou 310038, ChinaZhen ChenEnergy Research Institute, Nanyang Technological University, 637553, SingaporeLinyi BaiSchool of Physical and Mathematical Sciences, Nanyang Technological University, 637371, SingaporeHeping ShenSchool of Physical and Mathematical Sciences, Nanyang Technological University, 637371, SingaporeXiaoxu LiuKey Laboratory for Photonic and Electric Bandgap Materials, Heilongjiang University of Science and Technology, Harbin 150022, ChinaXinhui XiaState Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou 310027, ChinaYanli ZhaoSchool of Physical and Mathematical Sciences, Nanyang Technological University, 637371, SingaporeSerguei V. SavilovDepartment of Chemistry, Moscow State University, Moscow 119992, RussiaJianyi LinEnergy Research Institute, Nanyang Technological University, 637553, SingaporeZexiang ShenEnergy Research Institute, Nanyang Technological University, 637553, Singapore
2016en
ABI

Аннотация

The abundant reserve and low cost of sodium have provoked tremendous evolution of Na-ion batteries (SIBs) in the past few years, but their performances are still limited by either the specific capacity or rate capability. Attempts to pursue high rate ability with maintained high capacity in a single electrode remains even more challenging. Here, an elaborate self-branched 2D SnS2 (B-SnS2) nanoarray electrode is designed by a facile hot bath method for Na storage. This interesting electrode exhibits areal reversible capacity of ca. 3.7 mAh cm–2 (900 mAh g–1) and rate capability of 1.6 mAh cm–2 (400 mAh g–1) at 40 mA cm–2 (10 A g–1). Improved extrinsic pseudocapacitive contribution is demonstrated as the origin of fast kinetics of an alloying-based SnS2 electrode. Sodiation dynamics analysis based on first-principles calculations, ex-situ HRTEM, in situ impedance, and in situ Raman technologies verify the S-edge effect on the fast Na+ migration and reversible and sensitive structure evolution during high-rate charge/discharge. The excellent alloying-based pseudocapacitance and unsaturated edge effect enabled by self-branched surface nanoengineering could be a promising strategy for promoting development of SIBs with both high capacity and high rate response.

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