Covalent organic frameworks/carbon nanotubes composite with cobalt(II) pyrimidine sites for bifunctional oxygen electrocatalysis

With characteristics and advantages of functional composite materials, they are commendably adopted in numerous fields especially in oxygen electrocatalysis, which is due to the significant synergies between various components. Herein, a novel bifunctional oxygen electrocatalyst (Co-CNT@COF-Pyr) has...

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Published inNano materials science Vol. 6; no. 4; pp. 419 - 427
Main Authors Wu, Zhuangzhuang, Feng, Lijuan, Lu, Zhe, Yu, Xinxin, Zhao, Yuzhen, Luo, Junming, Wang, Shaolei, Tian, Xinlong, Chen, Qi
Format Journal Article
LanguageEnglish
Published Hong Kong Elsevier B.V 01.08.2024
KeAi Publishing Communications Ltd
KeAi Communications Co., Ltd
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Summary:With characteristics and advantages of functional composite materials, they are commendably adopted in numerous fields especially in oxygen electrocatalysis, which is due to the significant synergies between various components. Herein, a novel bifunctional oxygen electrocatalyst (Co-CNT@COF-Pyr) has been synthesized through in-situ growth of covalent organic frameworks (COFs) layers on the outer surface of highly conductive carbon nanotubes (CNTs) followed by coordination with Co(Ⅱ). For electrocatalytic OER, Co-CNT@COF-Pyr reveals a low overpotential (438 ​mV) in alkaline electrolyte (1.0 ​M aqueous solution of KOH) with a current density of 10 ​mA ​cm−2, which is comparable to most discovered COF-based catalysts. For electrocatalytic ORR, Co-CNT@COF-Pyr exhibits a low H2O2 yield range (9.0 ​%–10.1 ​%) and a reaction pathway close to 4e− (n ​= ​3.82–3.80) in alkaline electrolyte (0.1 ​M aqueous solution of KOH) within the test potential range of 0.1–0.6 ​V vs. RHE, which is superior to most reported COF-based catalysts. Hence, this research could not only offer an innovative insight into the construction of composites, but also facilitate the practical application of renewable fuel cells, closed water cycle, and rechargeable metal-air batteries. [Display omitted]
ISSN:2589-9651
2096-6482
2589-9651
DOI:10.1016/j.nanoms.2023.10.002