B.S. Shreemuke , P. Nitesh , T.R. Naveen Kumar , C. Sengottaiyan , Amreetha Seetharaman , Arun Thirumurugan , Manikandan Kandasamy , T. Kavinkumar
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Herein, we present a novel OER electrocatalyst (NFMN), fabricated by anchoring NF nanostructures onto a hybrid support of Mo<sub>2</sub>TiC<sub>2</sub>T<sub>X</sub> MXene (MX) and nitrogen-doped carbon (NC), which facilitates efficient electron transport. The resultant NFMN hybrid productively enhances the available surface area for catalytic interactions and improves the interface between the catalyst and the electrolyte. Notably, the strong synergistic electronic interactions among NF, MX, and NC in the NFMN catalyst result in outstanding OER performance, delivering a low overpotential of 259.7 mV at 100 mA cm<sup>−2</sup>, along with decent stability over 100 h. Besides, a water-splitting device was constructed using NFMN as the anode and commercial Pt/C as the cathode, requiring a cell voltage of only 1.52 V to achieve 10 mA cm<sup>−2</sup> in alkaline solution. More impressively, it also demonstrated excellent durability, maintaining stable performance for over 50 h. Density functional theory (DFT) calculations further unveil that the incorporation of MX and NC significantly enhances the OER activity by strengthening interactions with OER intermediates. Moreover, the charge transfer occurs across the interface in NF@MX and NF@NC hybrids, highlighting strong interfacial interactions. This work offers a new pathway for designing and engineering advanced hybrid materials for next-generation renewable energy applications.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"179 ","pages":"Article 151747"},"PeriodicalIF":8.3000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic activation of catalytic sites in NiFe−LDH architectures via coupling with nitrogen doped carbon/Mo2TiC2TX−MXene for high-efficiency alkaline oxygen evolution reaction\",\"authors\":\"B.S. 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引用次数: 0
摘要
电催化水裂解绿色制氢常常受到阳极析氧反应(OER)动力学缓慢的阻碍。因此,开发高效且具有成本效益的OER电催化剂对于解决日益增长的全球能源需求至关重要。在各种候选催化剂中,nfe - ldh (NF)纳米结构作为OER电催化剂表现出很大的前景;然而,它们的性能受到电子导电性差和活性催化位点暴露有限的严重阻碍。在此,我们提出了一种新的OER电催化剂(NFMN),通过将NF纳米结构锚定在Mo2TiC2TX MXene (MX)和氮掺杂碳(NC)的混合载体上制备,从而促进了高效的电子传递。所得的NFMN杂化物有效地提高了催化相互作用的可用表面积,并改善了催化剂和电解质之间的界面。值得注意的是,NFMN催化剂中NF、MX和NC之间的强协同电子相互作用导致了出色的OER性能,在100 mA cm - 2时提供了259.7 mV的低过电位,并且在100小时内具有良好的稳定性。此外,以NFMN为阳极,商用Pt/C为阴极构建了一个水分解装置,在碱性溶液中仅需要1.52 V的电池电压即可达到10 mA cm - 2。更令人印象深刻的是,它还表现出优异的耐久性,在超过50小时内保持稳定的性能。密度泛函理论(DFT)计算进一步揭示了MX和NC的结合通过加强与OER中间体的相互作用显著提高了OER活性。此外,在NF@MX和NF@NC杂化体中,电荷转移发生在界面上,突出了强的界面相互作用。这项工作为下一代可再生能源应用的先进混合材料的设计和工程提供了新的途径。
Synergistic activation of catalytic sites in NiFe−LDH architectures via coupling with nitrogen doped carbon/Mo2TiC2TX−MXene for high-efficiency alkaline oxygen evolution reaction
Green hydrogen production via electrocatalytic water splitting is often hindered by the sluggish kinetics of the oxygen evolution reaction (OER) at the anode. Therefore, developing highly efficient and cost-effective OER electrocatalysts is crucial in addressing the growing global energy demand. Among various candidates, NiFe–LDH (NF) nanostructures have shown great promise as OER electrocatalysts; however, their performance is significantly hindered by poor electronic conductivity and limited exposure of active catalytic sites. Herein, we present a novel OER electrocatalyst (NFMN), fabricated by anchoring NF nanostructures onto a hybrid support of Mo2TiC2TX MXene (MX) and nitrogen-doped carbon (NC), which facilitates efficient electron transport. The resultant NFMN hybrid productively enhances the available surface area for catalytic interactions and improves the interface between the catalyst and the electrolyte. Notably, the strong synergistic electronic interactions among NF, MX, and NC in the NFMN catalyst result in outstanding OER performance, delivering a low overpotential of 259.7 mV at 100 mA cm−2, along with decent stability over 100 h. Besides, a water-splitting device was constructed using NFMN as the anode and commercial Pt/C as the cathode, requiring a cell voltage of only 1.52 V to achieve 10 mA cm−2 in alkaline solution. More impressively, it also demonstrated excellent durability, maintaining stable performance for over 50 h. Density functional theory (DFT) calculations further unveil that the incorporation of MX and NC significantly enhances the OER activity by strengthening interactions with OER intermediates. Moreover, the charge transfer occurs across the interface in NF@MX and NF@NC hybrids, highlighting strong interfacial interactions. This work offers a new pathway for designing and engineering advanced hybrid materials for next-generation renewable energy applications.
期刊介绍:
The objective of the International Journal of Hydrogen Energy is to facilitate the exchange of new ideas, technological advancements, and research findings in the field of Hydrogen Energy among scientists and engineers worldwide. This journal showcases original research, both analytical and experimental, covering various aspects of Hydrogen Energy. These include production, storage, transmission, utilization, enabling technologies, environmental impact, economic considerations, and global perspectives on hydrogen and its carriers such as NH3, CH4, alcohols, etc.
The utilization aspect encompasses various methods such as thermochemical (combustion), photochemical, electrochemical (fuel cells), and nuclear conversion of hydrogen, hydrogen isotopes, and hydrogen carriers into thermal, mechanical, and electrical energies. The applications of these energies can be found in transportation (including aerospace), industrial, commercial, and residential sectors.