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Transition metal dichalcogenides (TMDs) such as MoSe2 have continued to generate interest in the engineering community because of their unique layered morphology—the strong in-plane chemical bonding between transition metal atoms sandwiched between two chalcogen atoms and the weak physical attraction between adjacent TMD layers provides them with not only chemical versatility but also a range of electronic, optical, and chemical properties that can be unlocked upon exfoliation into individual TMD layers. Such a layered morphology is particularly suitable for ion intercalation as well as for conversion chemistry with alkali metal ions for electrochemical energy storage applications. Nonetheless, host of issues including fast capacity decay arising due to volume changes and from TMD’s degradation reaction with electrolyte at low discharge potentials have restricted use in commercial batteries. One approach to overcome barriers associated with TMDs’ chemical stability functionalization of TMD surfaces by chemically robust precursor-derived ceramics or PDC materials, such as silicon oxycarbide (SiOC). SiOC-functionalized TMDs have shown to curb capacity degradation in TMD and improve long term cycling as Li-ion battery (LIBs) electrodes. Herein, we report synthesis of such a composite in which MoSe2 nanosheets are in SiOC matrix in a self-standing fiber mat configuration. This was achieved via electrospinning of TMD nanosheets suspended in pre-ceramic polymer followed by high temperature pyrolysis. Morphology and chemical composition of synthesized material was established by use of electron microscopy and spectroscopic technique. When tested as LIB electrode, the SiOC/MoSe2 fiber mats showed improved cycling stability over neat MoSe2 and neat SiOC electrodes. The freestanding composite electrode delivered a high charge capacity of 586 mAh g−1electrode with an initial coulombic efficiency of 58%. The composite electrode also showed good cycling stability over SiOC fiber mat electrode for over 100 cycles.
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This content will become publicly available on July 11, 2026
Curvature-Dependent Electrochemo-Mechanics of Silicon during Electrochemical Cycling
Silicon is an emerging anode material due to its high lithium storage capacity. While some commercial batteries now include silicon particles, porous three-dimensional (3D) scaffolded silicon electrodes may enable higher silicon loading by accommodating the silicon volume expansion during lithiation without significant electrode swelling. However, the electrochemomechanical response of silicon films on metal scaffolds remains poorly understood due to the complex scaffold morphology. We explore the role of scaffold curvature in the cycling behavior of silicon films and show that different curvatures exhibit distinctive failure modes. Negative curvature leads to crack opening from tensile and compressive stresses. Positive curvature induces tensile stress-driven buckling. Zero curvature exhibits fragmentation. The electrode morphology and chemistry for these systems are evaluated via scanning transmission electron microscopy with energy-dispersive X-ray spectroscopy (STEM-EDS). COMSOL Multiphysics simulations support that the electrochemo-mechanics of silicon are curvature-dependent. These findings point toward design strategies for 3D architected silicon anodes with improved cycling integrity.
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- Award ID(s):
- 2037898
- PAR ID:
- 10654473
- Publisher / Repository:
- ACS Publications
- Date Published:
- Journal Name:
- ACS Energy Letters
- Volume:
- 10
- Issue:
- 7
- ISSN:
- 2380-8195
- Page Range / eLocation ID:
- 3388 to 3394
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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