ArticleScientific reports2025
Flaky sputtered silicon MWCNTs core-shell structure as a freestanding binder-free electrode for lithium-ion battery.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
2 citing papers in PubMed.
- Vertically Integrated Silicon-Carbon Nanotube Architectures for High-Capacity and Robust Lithium-Ion Battery Anodes.ACS applied energy materials · 2026Article
- ZIF-8-derived hybrid nanocomposite platform with magnetic hematite nanoparticles as enhanced anode materials for lithium storage.RSC advances · 2025Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Core-shell silicon/multiwall carbon nanotubes are one of the most promising anode candidates for further improvement of lithium-ion batteries. Sufficient accommodation for massive volume expansion of silicon during the lithiation process and preventing pulverization and delamination with easy fabrication processes are still critical issues for practical applications. In this study, core-shell silicon/MWCNTs anode materials were synthesized using a facile and controllable PECVD technique to realize aligned MWCNTs followed by a silicon sputtering step. The use of the PECVD technique and the direct growth of multi-walled carbon nanotubes on the current collector creates a low tortuosity, flexible, and conductive scaffold, which, in addition to preventing CNT agglomeration, alleviates the pulverization and delamination of the silicon active material from the current collector, leading to the formation of an electrode with unique electrochemical performance. The CNT-Si core-shell electrode can achieve an excellent gravimetric specific capacity of 3250 mAh/g under a rate of C/5 and 99.8% capacity retention after more than 700 cycles. Electron microscopy revealed that the electrode structure has maintained its integrity and stability during long cycling (700 cycles and more). Apart from achieving high charging capacity, the use of such configuration leads to the formation of facile, inexpensive free-standing binder-free electrodes with no need to polymeric binders.
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