Temperature-dependent structural tuning of flower-like NiFe2O4 nanostructures as simplistic electrocatalyst for oxygen evolution reaction toward alkaline water splitting

IF 4.9 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Journal of Physics and Chemistry of Solids Pub Date : 2025-08-01 Epub Date: 2025-03-20 DOI:10.1016/j.jpcs.2025.112711
Sushama M. Nikam , Shubham D. Jituri , Shamal R. Shingte , Prashant B. Patil , Shoyebmohamad F. Shaikh , H.M. Pathan , Akbar I. Inamdar , Sarfraj H. Mujawar
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Abstract

Electrochemical water splitting is one of the best routes to produce highly demanding carbon-neutral green hydrogen using renewable energy sources. Therefore, oxygen evolution reaction (OER) which is bottleneck in electrocatalysis process due to its sluggish kinetics needs to be evaluated. In this work we fabricated flower like nickel ferrites with different annealing temperatures via chemical bath deposition technique and they are utilized for the OER properties. The nickel ferrite thin film annealed at 200 °C was found to be the most active OER electrocatalyst among the tested materials in 1 M KOH electrolyte. It exhibited an overpotential of 372 mV (vs RHE) at a current density of 20 mA cm2 and an ultralow Tafel slope of 42 mV dec−1 revealing faster reaction kinetics of the catalyst. Moreover, the catalysts showed outstanding electrochemical stability tested for more than 10 h of continuous operation in alkaline electrolyte without deviation in its overpotentials. It has been evidenced that the OER enhancement is due to the increased number of active sites, faster reaction kinetics (Rct = 0.42 Ω), hydrophilic surface properties, and high electrochemical surface area of 222 cm2. Thus, this work represents a simple and cost-effective way to develop catalyst materials for water splitting.
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花状NiFe2O4纳米结构作为碱水裂解析氧反应简单电催化剂的温度依赖结构调整
电化学水分解是利用可再生能源生产高要求碳中性绿色氢的最佳途径之一。因此,由于析氧反应动力学缓慢而成为电催化过程中的瓶颈,需要对其进行评价。本文采用化学浴沉积技术制备了不同退火温度的花状镍铁氧体,并将其用于OER性能的研究。在1 M KOH电解液中,经200℃退火的铁氧体镍薄膜是最活跃的OER电催化剂。在电流密度为20 mA cm−2时,其过电位为372 mV (vs RHE),超低塔菲尔斜率为42 mV dec−1,表明催化剂的反应动力学更快。此外,催化剂在碱性电解液中连续运行10 h以上,其过电位无偏差,表现出优异的电化学稳定性。OER的增强是由于活性位点的增加、反应动力学的加快(Rct = 0.42 Ω)、亲水性和222 cm2的高电化学表面积。因此,这项工作代表了一种简单而经济的方法来开发用于水分解的催化剂材料。
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来源期刊
Journal of Physics and Chemistry of Solids
Journal of Physics and Chemistry of Solids 工程技术-化学综合
CiteScore
7.80
自引率
2.50%
发文量
605
审稿时长
40 days
期刊介绍: The Journal of Physics and Chemistry of Solids is a well-established international medium for publication of archival research in condensed matter and materials sciences. Areas of interest broadly include experimental and theoretical research on electronic, magnetic, spectroscopic and structural properties as well as the statistical mechanics and thermodynamics of materials. The focus is on gaining physical and chemical insight into the properties and potential applications of condensed matter systems. Within the broad scope of the journal, beyond regular contributions, the editors have identified submissions in the following areas of physics and chemistry of solids to be of special current interest to the journal: Low-dimensional systems Exotic states of quantum electron matter including topological phases Energy conversion and storage Interfaces, nanoparticles and catalysts.
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