Diatomite‐Templated Synthesis of Single‐Atom Cobalt‐Doped MoS2/Carbon Composites to Boost Sodium Storage
Source abstract
Abstract
Abstract 2D transition metal dichalcogenides (TMDCs) and single‐atom catalysts (SACs) are promising electrodes for energy conversion/storage because of the layered structure and maximum atom utilization efficiency. However, the integration of such two type materials and the relevant sodium storage applications remain daunting challenges. Here, an ingenious diatomite‐templated synthetic strategy is designed to fabricate single‐atom cobalt‐doped MoS2/carbon (SA Co‐MoS2/C) composites toward the high‐performance sodium storage. Benefiting from the unique hierarchical structure, high electron/sodium‐ion conductivity, and abundant active sites, the obtained SA Co‐MoS2/C reveals remarkable specific capacity (≈604.0 mAh g−1 at 0.1 A g−1), high rate performance, and outstanding long cyclic stability. Particularly, the sodium‐ion full cell composed of SA Co‐MoS2/C anode and Na3V2(PO4)3 cathode demonstrates unexpected stability with the cycle number exceeded 1200. The internal sodium storage mechanism is clarified with the aid of density functional theory calculations and in situ experimental characterizations. This work not only represents a substantial leap in terms of synthesizing SACs on 2D TMDCs but also provides a crucial step toward the practical sodium‐ion battery applications.
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Research context
OpenAlex topics: Advancements in Battery Materials · MXene and MAX Phase Materials · Chemical Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
The Institute for Advanced Studies Wuhan University Wuhan 430072 P. R. China
Key Laboratory of Artificial Micro‐ and Nano‐structures of Ministry of Education School of Physics and Technology Wuhan University Wuhan 430072 P. R. China
Hubei Luojia Laboratory Wuhan 430072 P. R. China
Funding
National Natural Science Foundation of China · Fundamental Research Funds for the Central Universities
References (46)
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