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用于在酸性介质中高效析氢反应的铈掺杂二氧化钛修饰玻碳电极。

Ce-Doped TiO Fabricated Glassy Carbon Electrode for Efficient Hydrogen Evolution Reaction in Acidic Medium.

作者信息

Islam Md Nurnobi, Hossain Md Mosaraf, Maktedar Shrikant S, Rahaman Mostafizur, Rahman Mohammad Atiqur, Aldalbahi Ali, Hasnat Mohammad A

机构信息

Electrochemistry & Catalysis Research Laboratory (ECRL), Department of Chemistry, School of Physical Sciences, Shahjalal University of Science and Technology, Sylhet, 3114, Bangladesh.

Materials Chemistry & Engineering Research Laboratory, Department of Chemistry, National Institute of Technology, Srinagar, 190006, J & K (UT), India.

出版信息

Chem Asian J. 2024 Aug 19;19(16):e202301143. doi: 10.1002/asia.202301143. Epub 2024 Mar 28.

DOI:10.1002/asia.202301143
PMID:38376002
Abstract

The quest for sustainable and clean energy sources has intensified research on the Hydrogen Evolution Reaction (HER) in recent decades. In this study, we have presented a novel Ce-doped TiO catalyst synthesized through the sol-gel method, showcasing its potential as a superior electrocatalyst for HER in an acidic medium. Comprehensive characterization through X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Energy dispersive X-ray (EDX), and Raman spectroscopy confirms the successful formation of the catalyst. Electrocatalytic performance evaluation, including open circuit potential (OCP), electrochemical impedance spectroscopy (EIS), and Tafel analysis, demonstrates that GCE-5wt.%CeTiO outperforms bare GCE, as well as Ce and TiO-based electrodes. Kinetic investigations reveal a Tafel slope of 105 mV dec, indicating the Volmer step as the rate-determining step. The onset potential for HER at GCE-5wt.%CeTiO is -0.16 V vs. RHE, close to the platinum electrode. Notably, the catalyst exhibits a low overpotential of 401 mV to achieve a current density of 10 mA cm with an impressive 95 % Faradaic efficiency. Furthermore, the catalyst demonstrates outstanding durability, maintaining a negligible increase in overpotential during a 14-hour chronoamperometry test. These results have far-reaching implications for the development of cost-effective and efficient electrocatalysts for hydrogen production.

摘要

近几十年来,对可持续和清洁能源的追求强化了对析氢反应(HER)的研究。在本研究中,我们展示了一种通过溶胶-凝胶法合成的新型铈掺杂二氧化钛催化剂,该催化剂在酸性介质中作为HER的优异电催化剂具有很大潜力。通过X射线衍射(XRD)、X射线光电子能谱(XPS)、能量色散X射线(EDX)和拉曼光谱进行的综合表征证实了催化剂的成功合成。电催化性能评估,包括开路电位(OCP)、电化学阻抗谱(EIS)和塔菲尔分析,表明玻碳电极负载5wt.%铈的二氧化钛(GCE-5wt.%CeTiO)优于裸玻碳电极以及基于铈和二氧化钛的电极。动力学研究表明塔菲尔斜率为105 mV dec,表明Volmer步骤是速率决定步骤。GCE-5wt.%CeTiO上HER的起始电位相对于可逆氢电极(RHE)为-0.16 V,接近铂电极。值得注意的是,该催化剂实现10 mA cm的电流密度时过电位低至401 mV,法拉第效率高达95%。此外,该催化剂表现出出色的耐久性,在14小时的计时电流法测试中过电位增加可忽略不计。这些结果对开发用于制氢的经济高效电催化剂具有深远意义。

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