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从第一性原理预测看二维过渡金属二卤族化合物作为钾离子电池有前途的阳极

Two-dimensional transition metal dichalcogenides as promising anodes for potassium ion batteries from first-principles prediction.

机构信息

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, Jiangsu 215123, China.

出版信息

Phys Chem Chem Phys. 2019 Nov 14;21(42):23441-23446. doi: 10.1039/c9cp03948a. Epub 2019 Oct 16.

Abstract

Two-dimensional (2D) materials are expected to be utilized as electrodes for alkali metal ion batteries due to their exceptional properties, but the larger size of K ions has been supposed to induce structural collapses and low charge-discharge efficiency. In this work, we propose transition metal dichalcogenide (TMD) materials as the anode electrodes for potassium ion batteries (PIBs). K ions can stably be adsorbed on most of the TMD materials with strong adsorption energies, and the structural phase transition from the 2H phase to the 1T phase can further enhance the K adsorption. It is surprising that, the diffusion barriers for K ions on TMD monolayers are low enough (less than 0.05 eV) to allow K ions to freely migrate. Among the TMD materials that we consider here, both VS and TiS exhibit extraordinary properties with good electronic conductivity, fast K diffusion, optimal open circuit voltage and high theoretical K storage capacity, which are promising anode materials for K ion batteries.

摘要

二维(2D)材料有望被用作碱金属离子电池的电极,因为它们具有特殊的性质,但由于 K 离子的尺寸较大,可能会导致结构坍塌和低充放电效率。在这项工作中,我们提出将过渡金属二卤化物(TMD)材料作为钾离子电池(PIBs)的阳极电极。大多数 TMD 材料对 K 离子具有较强的吸附能,可稳定地吸附 K 离子,且从 2H 相到 1T 相的结构相变可进一步增强 K 吸附。令人惊讶的是,TMD 单层上 K 离子的扩散势垒足够低(小于 0.05 eV),允许 K 离子自由迁移。在我们考虑的 TMD 材料中,VS 和 TiS 都表现出良好的电子导电性、快速的 K 扩散、最优的开路电压和高理论 K 存储容量等优异性能,是钾离子电池有前途的阳极材料。

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