Designing NiCoS/CNTs composites for highly efficient bifunctional electrocatalyst in water splitting

IF 2.4 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2024-09-12 DOI:10.1007/s11581-024-05818-5
Sheraz Yousaf, Safaa N. Abdou, Tabinda Rasheed, Mohamed M. Ibrahim, Imran Shakir, Salah M. El-Bahy, Iqbal Ahmad, Muhammad Shahid, Muhammad Farooq Warsi
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Abstract

Electrocatalytic water-splitting holds great promise for the large-scale production of hydrogen as a renewable and environmentally friendly alternative to fossil fuels. However, the exploration of a cost-effective, stable, and active bifunctional electrocatalyst remains a significant challenge in achieving efficient hydrogen (H2)/oxygen (O2) production through water electrolysis. Herein, we used nickel-doped cobalt sulfide (NiCoS) supported by carbon nanotubes (CNTs) as a promising candidate for electrocatalytic water splitting. The Ni-Co-based catalyst comprising the redox couples of Ni+3/Ni+2 and Co+3/Co+2 exhibits remarkable efficiency as active sites for both HER as well as OER. The linear sweep voltammetry (LSV) results indicate that the fabricated bifunctional catalyst necessitates overpotentials of just 327 mV for achieving a cathodic current density of 100 mAcm−2 and 344 mV for the anodic current density of the same value. Additionally, the Tafel slopes for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are 64 mVdec−1 and 70 mVdec−1, respectively. The electrochemical impedance analysis (EIS) was also performed which revealed that NiCoS/CNTs has the lowest charge transfer resistance (Rct) which is 1.94 Ω as compared to the CoS (7.52 Ω) and NiCoS (4.74Ω). The ECSA value of the prepared NiCoS/CNTs material was observed as 3.47 cm2. Such an excellent synergetic effect is due to the interaction of NiCoS with CNTs, which not only provides highly active sites available for faster charge transfer but also increases the electrical conductivity of the fabricated material. This study offers valuable insights into the design of the best electrocatalysts for water splitting.

Abstract Image

设计用于高效双功能水分离电催化剂的 NiCoS/CNTs 复合材料
电催化水分离技术在大规模生产氢气方面大有可为,它是一种可再生和环保的化石燃料替代品。然而,在通过电解水实现高效制氢(H2)/制氧(O2)的过程中,探索具有成本效益、稳定和活性的双功能电催化剂仍然是一项重大挑战。在此,我们将掺杂镍的硫化钴(NiCoS)与碳纳米管(CNTs)作为电催化水分离的候选催化剂。由 Ni+3/Ni+2 和 Co+3/Co+2 氧化还原偶组成的镍钴基催化剂作为 HER 和 OER 的活性位点,表现出显著的效率。线性扫描伏安法(LSV)结果表明,制备的双功能催化剂在达到 100 mAcm-2 的阴极电流密度时只需 327 mV 的过电位,在达到相同的阳极电流密度时只需 344 mV 的过电位。此外,氢进化反应(HER)和氧进化反应(OER)的塔菲尔斜率分别为 64 mVdec-1 和 70 mVdec-1。此外,还进行了电化学阻抗分析(EIS),结果表明与 CoS(7.52 Ω)和 NiCoS(4.74Ω)相比,NiCoS/CNTs 的电荷转移电阻(Rct)最低,为 1.94 Ω。制备的 NiCoS/CNTs 材料的 ECSA 值为 3.47 平方厘米。之所以能产生如此出色的协同效应,是因为镍钴锰酸锂与碳纳米管之间的相互作用不仅为电荷的快速转移提供了高活性位点,还提高了制备材料的导电性。这项研究为设计最佳的水分离电催化剂提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
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