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用于超级电容器电极的、由双金属分子框架微棒引发的杂原子掺杂纳米多孔碳。

Heteroatom-doped nanoporous carbon initiated from bimetallic molecular framework micro-rods for supercapacitor electrodes.

作者信息

Wang Qiang, Liang Hongwei, Wu Dun

机构信息

School of Materials Science and Engineering, Changzhou University 213164 P. R. China

Huaide College, Changzhou University 214500 P. R. China.

出版信息

RSC Adv. 2019 Jun 4;9(31):17521-17529. doi: 10.1039/c9ra02533b.

Abstract

We report herein that zinc and cobalt bimetallic-organic-framework (BMOF) crystalline micro-rods are able to be constructed instantly with the eco-friendly glutamate ligand and building unit of double metallic ions. After carbonization and acid leaching of these precursors, the resultant heteroatom-doped porous carbon occupies not only the enriched mesopore architectures but the ultrathin graphitic networks. Moreover, due to cyclizing dehydration reaction of the glutamate ligand upon thermal conversion, the predominant pyrrolic and pyridinic nitrogen atom sites within the carbon lattices are achieved. The supercapacitor electrodes from these carbonaceous materials without any conductive addictive deliver an impressive specific gravimetric capacitance of 230 F g and a specific areal capacitance of 50 μF cm at a current density of 1 A g in alkaline aqueous electrolyte.

摘要

我们在此报告,锌钴双金属有机框架(BMOF)晶体微棒能够通过环保型谷氨酸配体和双金属离子构建单元即时构建。对这些前驱体进行碳化和酸浸后,所得杂原子掺杂多孔碳不仅具有丰富的中孔结构,还具有超薄石墨网络。此外,由于谷氨酸配体在热转化时发生环化脱水反应,在碳晶格中形成了主要的吡咯型和吡啶型氮原子位点。这些不含任何导电添加剂的碳质材料制成的超级电容器电极,在碱性水电解质中,电流密度为1 A g时,展现出令人印象深刻的230 F g比重量电容和50 μF cm比面积电容。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2592/9064546/ff4d5a9edcae/c9ra02533b-f1.jpg

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