Thermodynamically Stable Synthesis of the 1T-MoS<sub>2</sub>/g-CN Superstructure with Rapid Redox Kinetics for Robust Capacitive Energy Storage.
basic_science · Level V
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- Record sourced from PubMed, PMID 40012176.
- Also identified by DOI 10.1021/acsnano.5c00717.
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Abstract
Artificial superstructures with advanced physicochemical properties and electronic interfaces are of great importance for capacitive energy storage. Herein, by one-step phase transition and interfacial bridging, we achieve thermodynamically stable synthesis of the 1T-MoS<sub>2</sub>/graphitic carbon nitride (g-CN) superstructure, where the carbon atoms of g-CN are covalently bridged on molybdenum atoms of the 1T phase molybdenum disulfide (1T-MoS<sub>2</sub>) interface via C-Mo bonds. The DFT and MD calculations reveal that the 1T-MoS<sub>2</sub>/g-CN superstructure with a strong interfacial interaction (covalent character: 97%), superior electron conduction (d-band center: -1.2 eV), abundant accessible channels (free volume: 53% whole space), and expedited redox kinetics (reaction energy barriers: 0.9 eV) can enhance interfacial charge transfer and faradaic ion accumulation. Therefore, the 1T-MoS<sub>2</sub>/g-CN superstructure delivers a high specific capacitance of 2080 F g<sup>-1</sup> and excellent structural stability in KOH solution. Moreover, the solid-polymer-electrolyte chip-based 1T-MoS<sub>2</sub>/g-CN supercapacitors can achieve a large energy density (73 mWh g<sup>-1</sup>), outstanding cycling stability (91% capacitance retention after 10,000 cycles), and desired self-powered application.