0 Datasets
0 Files
Get instant academic access to this publication’s datasets.
Yes. After verification, you can browse and download datasets at no cost. Some premium assets may require author approval.
Files are stored on encrypted storage. Access is restricted to verified users and all downloads are logged.
Yes, message the author after sign-up to request supplementary files or replication code.
Join 50,000+ researchers worldwide. Get instant access to peer-reviewed datasets, advanced analytics, and global collaboration tools.
✓ Immediate verification • ✓ Free institutional access • ✓ Global collaborationJoin our academic network to download verified datasets and collaborate with researchers worldwide.
Get Free AccessA facile and novel method for the fabrication of core‐shell nanoparticles (PTMA@SiO 2 ) based on a poly(2,2,6,6‐tetramethylpiperidinyloxy‐4‐yl methacrylate) (PTMA) core and a porous SiO 2 shell is reported. The core‐shell nanoparticles are further self‐assembled with negatively charged multi‐walled carbon nanotubes (MWCNTs), which results in the formation of a free‐standing cathode electrode. The porous SiO 2 shell not only effectively improves the stability of the linear PTMA redox polymer with low molar mass in organic electrolytes but also leads to the uniform dispersion of PTMA active units in the MWCNTs conductive network. The PTMA@SiO 2 @MWCNT composite electrode exhibits a specific capacity as high as 73.8 mAh g at 1 C and only 0.11% capacity loss per cycle at a rate of 2 C.
He Jia, Christian Friebe, Ulrich Sigmar Schubert, Xiaozhe Zhang, Ting Quan, Yan Lü, Jean‐François Gohy (2019). Core‐Shell Nanoparticles with a Redox Polymer Core and a Silica Porous Shell as High‐Performance Cathode Material for Lithium‐Ion Batteries. , 8(3), DOI: https://doi.org/10.1002/ente.201901040.
Datasets shared by verified academics with rich metadata and previews.
Authors choose access levels; downloads are logged for transparency.
Students and faculty get instant access after verification.
Type
Article
Year
2019
Authors
7
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1002/ente.201901040
Access datasets from 50,000+ researchers worldwide with institutional verification.
Get Free Access