A Tunable 3D Nanostructured Conductive Gel Framework Electrode for High‐Performance Lithium Ion Batteries

This study develops a tunable 3D nanostructured conductive gel framework as both binder and conductive framework for lithium ion batteries. A 3D nanostructured gel framework with continuous electron pathways can provide hierarchical pores for ion transport and form uniform coatings on each active pa...

Full description

Saved in:
Bibliographic Details
Published inAdvanced materials (Weinheim) Vol. 29; no. 22
Main Authors Shi, Ye, Zhang, Jun, Bruck, Andrea M., Zhang, Yiman, Li, Jing, Stach, Eric A., Takeuchi, Kenneth J., Marschilok, Amy C., Takeuchi, Esther S., Yu, Guihua
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.06.2017
Wiley
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:This study develops a tunable 3D nanostructured conductive gel framework as both binder and conductive framework for lithium ion batteries. A 3D nanostructured gel framework with continuous electron pathways can provide hierarchical pores for ion transport and form uniform coatings on each active particle against aggregation. The hybrid gel electrodes based on a polypyrrole gel framework and Fe3O4 nanoparticles as a model system in this study demonstrate the best rate performance, the highest achieved mass ratio of active materials, and the highest achieved specific capacities when considering total electrode mass, compared to current literature. This 3D nanostructured gel‐based framework represents a powerful platform for various electrochemically active materials to enable the next‐generation high‐energy batteries. A tunable 3D nanostructured gel framework with continuous electron pathways can provide hierarchical pores for ion transport and form uniform coatings on each active particle against aggregation. The hybrid gel electrodes based on a polypyrrole gel framework and Fe3O4 nanoparticles demonstrate one of the best rate performances and the highest achieved specific capacities when considering total electrode mass.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
USDOE Office of Science (SC), Basic Energy Sciences (BES)
SC0012673
ISSN:0935-9648
1521-4095
1521-4095
DOI:10.1002/adma.201603922