Boosting the electrochemical water splitting efficiency of Copper Vanadium Oxide by Annealing method

IF 2.3 4区 材料科学 Q2 MATERIALS SCIENCE, CERAMICS
Sheraz Yousaf, Mohammad Altaf, Mohd Zahid Ansari
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Abstract

Electrocatalytic water-splitting is one of the promising processes for producing hydrogen as a renewable and ecologically friendly fuel replacing fossil fuel. Achieving cost-efficient, stable, and active bifunctional electrocatalysts through water electrolysis is the highest challenge as the highest rate of hydrogen and oxygen production is desired. The role of copper vanadium oxide in different annealing conditions, as a possible electrocatalyst for water splitting was investigated in terms of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Structural and morphological characterizations were done by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The electrocatalytic efficiency and stability were assessed by linear sweep voltammetry (LSV) and chronoamperometry (CA). The LSV measurements show that the copper vanadium oxide catalyst with 700 °C annealing temperature exhibited overpotentials of 232 mV and 260 mV to attain a cathodic current density of 10 mAcm−2 and anodic current density of 20 mAcm−2, respectively. A Tafel slope of 68 mVdec−1 was required for the HER and for OER a Tafel slope of 72 mVdec−1 was needed. In addition, stability tests regarding CA yield very good stability of the material. The high annealing temperatures are important as they restructure crystal structures, increase the number of active sites, and thus improve electrical conductivity. Consequently, the overpotentials for OER and HER decrease due to enhanced electron transfer efficiency causing favorable interactions between electrocatalysts and reactants. The current research highlights the capability of the copper vanadium oxide catalyst for water water-splitting process which is cost-effective and efficient for renewable hydrogen production.

Graphical Abstract

Schematic diagram illustrating the mechanism and overall theme of the current manuscript.

Abstract Image

Abstract Image

用退火法提高氧化铜钒的电化学水分离效率
电催化水分离是一种很有前景的制氢工艺,可作为替代化石燃料的可再生和生态友好型燃料。通过水电解实现具有成本效益、稳定和活性的双功能电催化剂是最大的挑战,因为人们希望获得最高的氢气和氧气生产率。研究人员从氢进化反应(HER)和氧进化反应(OER)的角度研究了不同退火条件下的铜钒氧化物作为一种可能的水分离电催化剂的作用。通过 X 射线衍射 (XRD)、傅立叶变换红外光谱 (FTIR) 和扫描电子显微镜 (SEM) 对其结构和形态进行了表征。电催化效率和稳定性通过线性扫频伏安法(LSV)和计时电流法(CA)进行了评估。LSV 测量结果表明,退火温度为 700 °C 的氧化铜钒催化剂在达到 10 mAcm-2 的阴极电流密度和 20 mAcm-2 的阳极电流密度时,过电位分别为 232 mV 和 260 mV。HER 所需的塔菲尔斜率为 68 mVdec-1,OER 所需的塔菲尔斜率为 72 mVdec-1。此外,有关 CA 的稳定性测试表明该材料具有非常好的稳定性。高温退火非常重要,因为它可以重组晶体结构,增加活性位点的数量,从而提高导电性。因此,由于电子传递效率的提高导致电催化剂和反应物之间产生有利的相互作用,OER 和 HER 的过电位也随之降低。目前的研究突显了铜钒氧化物催化剂在水分离过程中的能力,这种催化剂对于可再生氢气的生产具有成本效益和效率。
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来源期刊
Journal of Sol-Gel Science and Technology
Journal of Sol-Gel Science and Technology 工程技术-材料科学:硅酸盐
CiteScore
4.70
自引率
4.00%
发文量
280
审稿时长
2.1 months
期刊介绍: The primary objective of the Journal of Sol-Gel Science and Technology (JSST), the official journal of the International Sol-Gel Society, is to provide an international forum for the dissemination of scientific, technological, and general knowledge about materials processed by chemical nanotechnologies known as the "sol-gel" process. The materials of interest include gels, gel-derived glasses, ceramics in form of nano- and micro-powders, bulk, fibres, thin films and coatings as well as more recent materials such as hybrid organic-inorganic materials and composites. Such materials exhibit a wide range of optical, electronic, magnetic, chemical, environmental, and biomedical properties and functionalities. Methods for producing sol-gel-derived materials and the industrial uses of these materials are also of great interest.
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