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二维镍有机框架修饰的碳纳米管封装镍纳米颗粒用于高效的碳氮键和氧氢键裂解

2D Ni-organic frameworks decorated carbon nanotubes encapsulated Ni nanoparticles for robust CN and HO bonds cleavage.

作者信息

Xie Yuhua, Xiong Tiantian, Li Chen, Shi Han, Zhou Cong, Luo Fang, Yang Zehui

机构信息

Hubei Hydrogen Energy Technology Innovation Center, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, PR China.

College of Materials Science and Engineering, State Key Laboratory of New Textile Materials & Advanced Processing Technology, Wuhan Textile University, Wuhan 430200, PR China.

出版信息

J Colloid Interface Sci. 2023 Dec 15;652(Pt A):41-49. doi: 10.1016/j.jcis.2023.08.063. Epub 2023 Aug 10.

Abstract

In this work, we report a robust bifunctional electrocatalyst composed of 2D Ni- organic frameworks (Ni-MOF) and nitrogen doped carbon nanotubes encapsulated Ni nanoparticles (Ni-MOF@Ni-NCNT) for CN and HO bonds dissociation. Due to the presence of Ni-NCNT, adsorption of OH species is enhanced and CO binding strength is simultaneously weakened leading to a boosted urea oxidation reaction performance reflected by decrement in potential at 100 mA cm by 69 mV. The loosened binding strength with CO specie is highlighted by in-situ electrochemical impedance spectroscopy (EIS) test and DFT calculation. Moreover, the alkaline hydrogen evolution reaction (HER) performance of Ni-MOF@Ni-NCNT is better than Ni-MOF and Ni-NCNT evidenced by the overpotential at 50 mA cm decreased by 224 mV and 900 mV ascribed to the synergistic effect, in which Ni-MOF, Ni nanoparticles and Ni-Nx-C facilitates water adsorption, dissociation and adsorption/combination of hydrogen ions, respectively. The assembled HER- urea oxidation reaction (UOR) system requires only 1.33 V to reach 10 mA cm, 70 mV lower than water splitting driven by Pt/C-IrO.

摘要

在本工作中,我们报道了一种由二维镍有机框架(Ni-MOF)和氮掺杂碳纳米管包裹的镍纳米颗粒(Ni-MOF@Ni-NCNT)组成的用于C-N和O-H键解离的稳健双功能电催化剂。由于Ni-NCNT的存在,OH物种的吸附增强,同时CO的结合强度减弱,导致尿素氧化反应性能得到提升,这体现在100 mA cm⁻²时的电位降低了69 mV。原位电化学阻抗谱(EIS)测试和密度泛函理论(DFT)计算突出了与CO物种的结合强度的减弱。此外,Ni-MOF@Ni-NCNT的碱性析氢反应(HER)性能优于Ni-MOF和Ni-NCNT,50 mA cm⁻²时的过电位分别降低了224 mV和900 mV,这归因于协同效应,其中Ni-MOF、镍纳米颗粒和Ni-Nx-C分别促进了水的吸附、解离以及氢离子的吸附/结合。组装的HER-尿素氧化反应(UOR)系统仅需1.33 V就能达到10 mA cm⁻²,比由Pt/C-IrO驱动的水分解低70 mV。

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