Integrating the Essence of a Metal–Organic Framework with Electrospinning: A New Approach for Making a Metal Nanoparticle Confined N‑Doped Carbon Nanotubes/Porous Carbon Nanofibrous Membrane for Energy Storage and Conversion

The fabrication of an economic and efficient multifunctional advanced nanomaterial with a rational composition and configuration by a facile methodology is a crucial challenge. Herein, we are the first to report the growth of Co nanoparticle-integrated nitrogen-doped carbon nanotubes (N-CNTs) on por...

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Published inACS applied materials & interfaces Vol. 13; no. 20; pp. 23732 - 23742
Main Authors Mukhiya, Tanka, Muthurasu, Alagan, Tiwari, Arjun Prasad, Chhetri, Kisan, Chae, Su-Hyeong, Kim, Hyoju, Dahal, Bipeen, Lee, Byoung Min, Kim, Hak Yong
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 26.05.2021
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Summary:The fabrication of an economic and efficient multifunctional advanced nanomaterial with a rational composition and configuration by a facile methodology is a crucial challenge. Herein, we are the first to report the growth of Co nanoparticle-integrated nitrogen-doped carbon nanotubes (N-CNTs) on porous carbon nanofibers by simply heating in the situ-developed metal–organic framework (MOF)-based electrospun nanofibrous membrane with no need for an external supply of any additional precursors and reducing gases. The long and entangled N-CNTs originating from highly porous and graphitic carbon nanofibers offer good flexibility, large surface area, high porosity, high conductivity, the homogeneous incorporation of heteroatoms and metallic constituents, and an abundant exposure of active nanocatalytic sites. The as-developed nanoassembly demonstrates attractive characteristics for electrocatalytic hydrogen and oxygen evolution reactions and electrochemical energy storage. This strategy of integrating the essence of an MOF with electrospinning offers a new, direct, and cost-effective approach for making N-doped CNT-based multifunctional membranes.
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ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.1c04104