Highly Conductive Mo2C Nanofibers Encapsulated in Ultrathin MnO2 Nanosheets as a Self-Supported Electrode for High-Performance Capacitive Energy Storage
Source abstract
Abstract
Nanostructured transition metal carbides (TMCs) with superior electrochemical properties are promising materials for high-efficiency energy-storage applications. Herein one-dimensional molybdenum carbide nanofibers (Mo 2 C NFs) have been fabricated by a facile and effective electrospinning strategy. Based on the cross-linked network architecture with ultrahigh electronic conductivity, each Mo 2 C NF is uniformly encapsulated in lamellar manganese dioxide (MnO 2 ) via electrodeposition, forming a self-supported MnO 2 –Mo 2 C NF film with excellent electrochemical activity. Remarkably, the highly conductive inner layer of porous Mo 2 C NFs acts like a “highway” to facilitate charge transport and ionic diffusion, while the MnO 2 nanosheets with abundant active area are favorable for the accumulation of effective electric charges. Benefiting from these features, the hybrid film is directly applied as the self-standing electrode of supercapacitors (SCs) without any additives, which delivers considerably large specific capacitance with strong durability in both aqueous and organic (ionic liquid) electrolytes. This work elucidates a feasible way toward heteronanofiber engineering of TMCs on a promising additive-free electrode for flexible and high-performance SCs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Advancements in Battery Materials · MXene and MAX Phase Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory for Metallic Matrix Composite Materials, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China
Funding
Shanghai Jiao Tong University · National Natural Science Foundation of China · 211 Project for Advanced Materials Science
References (54)
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