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通过与UiO-66金属有机框架形成杂化物提高MoC纳米颗粒的整体电催化析氢效率

Enhancing the Overall Electrocatalytic Water-Splitting Efficiency of MoC Nanoparticles by Forming Hybrids with UiO-66 MOF.

作者信息

Ali Maryum, Pervaiz Erum, Rabi Osama

机构信息

Department of Chemical Engineering, School of Chemical and Materials Engineering (SCME), National University of Sciences & Technology (NUST), Sector H-12, Islamabad 44000, Pakistan.

出版信息

ACS Omega. 2021 Dec 6;6(50):34219-34228. doi: 10.1021/acsomega.1c03115. eCollection 2021 Dec 21.

Abstract

For efficient electrocatalytic water-splitting, developing a nonprecious-metal-based stable and highly active material is the most challenging task. In this paper, we have devised a synthesis strategy for a hybrid catalyst composed of molybdenum carbide (MoC) and a Zr-based metal-organic framework (MOF) (UiO-66) via the solvothermal process. Synergistic effects between MoC and UiO-66 lead to a decrease in the hydrogen adsorption energy on the catalysts, and MoC/UiO-66 hybrids offer excellent catalytic activity in an alkaline environment for water-splitting. Particularly, the optimized MoC/UiO-66 hybrid, termed MCU-2 with 50:50 wt % of both components, displayed the best catalytic performance for both hydrogen and oxygen evolution reactions (HER/OER). It offered a small overpotential of 174.1 mV to attain a current density of 10 mA/cm and a Tafel plot value of 147 mV/dec for HER. It also offered a low overpotential of around 180 mV to attain a current density of 20 mA/cm and a Tafel plot value of 134 mV/dec for OER. Additionally, the catalyst was stable for over 24 h and ∼1000 cycles with a very minute shift in performance, and the electrolyzer indicates that a potential of ∼1.3 V is required to reach 10 mA/cm current density. It can be inferred from the results that the MoC/UiO-66 hybrid is a promising candidate as a nonexpensive and active catalyst for overall electrocatalytic water-splitting as the devised catalyst exhibits enhanced kinetics for both OER and HER, a more exposed surface area, faster electron transport, and enhanced diffusion of the electrolyte.

摘要

对于高效的电催化水分解而言,开发一种基于非贵金属的稳定且高活性材料是最具挑战性的任务。在本文中,我们通过溶剂热法设计了一种由碳化钼(MoC)和锆基金属有机框架(MOF)(UiO - 66)组成的混合催化剂的合成策略。MoC和UiO - 66之间的协同效应导致催化剂上氢吸附能降低,并且MoC/UiO - 66混合物在碱性环境中对水分解具有优异的催化活性。特别地,优化后的MoC/UiO - 66混合物,即两种组分重量比为50:50的MCU - 2,在析氢反应和析氧反应(HER/OER)中均表现出最佳的催化性能。对于HER,它达到10 mA/cm²电流密度时的过电位仅为174.1 mV,塔菲尔斜率值为147 mV/dec。对于OER,它达到20 mA/cm²电流密度时的过电位约为180 mV,塔菲尔斜率值为134 mV/dec。此外,该催化剂在超过24小时和大约1000次循环中保持稳定,性能仅有非常微小的变化,并且该电解槽表明达到10 mA/cm²电流密度需要约1.3 V的电位。从结果可以推断,MoC/UiO - 66混合物作为一种用于整体电催化水分解的廉价且活性催化剂是一个有前景的候选材料,因为所设计的催化剂在OER和HER中均表现出增强的动力学、更大的暴露表面积、更快的电子传输以及增强的电解质扩散。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0710/8696999/4a4ba45a7a8c/ao1c03115_0002.jpg

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