Confinement and Self‐Supply of Carbon Sources by Micro‐Containers Enable Efficient In Situ Growth of Carbon Nanotubes for Li‐Ion Storage
Source abstract
Abstract
ABSTRACT Confinement effects generated by micro/nanoscale physical spaces for chemical reactions may enable to effectively modulate nanostructures or create novel nanostructures by remarkably changing reaction kinetics and behaviors, which needs to be explored. Herein, a productive and up‐scalable approach is proposed for in situ growth of nitrogen‐doped carbon nanotubes (N/CNTs) by introducing commercial expanded graphites (EGs) as micro‐containers for enhancement of reaction rates and reduction of energy costs. With the solid carbonaceous (polyvinylpyrrolidone, PVP) and catalytic (Fe‐based or Co‐based) precursors incubated in the micro‐containers, the local sufficient self‐supply of C/N sources ensures the in situ growth of high‐quality N/CNTs with a high yield over 14% and a faster formation rate compared to a conventional open configuration. Growth behavior, morphology, and structure of products are conditioned by the dimension and structure of micro‐containers, the ratio of source/catalyst precursors, and pyrolyzation temperature. The N/CNTs‐based hierarchical architectures are demonstrated to have superior Li‐ion storage performance as anode materials, say, a capacity of 1129.5 mAh g −1 at 0.05 A g −1 and a retention of 99.5% (95.0%) for 0.1 A g −1 (10 A g −1 ) after 100 (10 000) cycles. This strategy can be generalized for the preparation of other nanostructures.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Electrocatalysts for Energy Conversion · Catalysis for Biomass Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nanofabrication Laboratory National Center for Nanoscience and Technology Beijing P. R. China
Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing P. R. China
Funding
National Natural Science Foundation of China · Shanghai Institute of Technical Physics, Chinese Academy of Sciences
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