Bifunctional Nd2Se3–Mn2O3 heterostructure nanospheres for enhanced alkaline water splitting via interface engineering

IF 8.1 2区 工程技术 Q1 CHEMISTRY, PHYSICAL
M. Abdul , Chingmai Ko , Xiaoyan Tang , Mostafa A. Ismail , Sana Ben Khalifa , Taoufik Saidani , Saleh Chebaane , Jehan Akbar
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引用次数: 0

Abstract

The advancement of high-efficiency, durable, and inexpensive catalysts is essential for electrocatalytic water electrolysis to gain sustainable hydrogen energy. Catalysts based on noble metals (Pt, Pd for HER and Ir, Ru for OER) are efficient and benchmark towards water electrolysis, but high cost, scarcity, and lower stability prevent their applicability for industrial application. Up to now, rare earth/transition metal catalysts are still not more efficient and durable for water electrolysis. Herein, we report a Nd2Se3–Mn2O3 heterojunction assembled on stainless steel (SS) using a hydrothermal method to ameliorate the properties of electrocatalysts via interface engineering for HER, OER, and overall water splitting. Under comparison with two pure electrocatalysts (Nd2Se3 and Mn2O3), the full water splitting performance is checked in 3 and 2-electrolysis systems using the alkaline medium. Here, different physical characterization like XRD and TEM/EDX showed that the strong combination of two materials (Nd2Se3 and Mn2O3) leads to the structural reconstruction of precursor and spherical formation with an increasing number of disordered pores and active sites. Besides, XPS confirmed the strong electronic coupling, which enhances the adsorption of hydrogen atoms on the catalyst surface compared to pure ones. At 10 mA cm−2, Nd2Se3–Mn2O3 delivers the smallest overpotential of 260 and 121 mV for OER and HER, indicating that coupling effects of Nd2Se3 and Mn2O3 are responsible for boosting the catalytic performances. The effect of small charge transfer resistance and large surface area for HER-OER about bifunctional electrocatalysts is confirmed using EIS and Cdl. Furthermore, an assembled Nd2Se3–Mn2O3//Nd2Se3–Mn2O3 device in a 2-electrode electrolyzer exhibited a cell voltage of 1.47 V along with excellent stability of 96 h at 10 mA cm−2 for overall water splitting. This work paves the way for regulating the interface effect of bifunctional catalysts through heterojunctions to develop efficient and durable electrocatalysts.
基于界面工程的双功能Nd2Se3-Mn2O3异质结构纳米球增强碱性水裂解
高效、耐用、廉价的催化剂是电催化水电解获得可持续氢能的关键。基于贵金属的催化剂(HER为Pt, Pd, Ir, Ru)是高效的水电解基准,但成本高,稀缺性和较低的稳定性阻碍了它们在工业应用中的适用性。到目前为止,稀土/过渡金属催化剂在水电解中仍然不是更高效和耐用的。本文报道了采用水热方法在不锈钢(SS)上组装Nd2Se3-Mn2O3异质结,通过界面工程改善电催化剂的性能,用于HER, OER和整体水分解。通过与两种纯电催化剂(Nd2Se3和Mn2O3)的对比,考察了该催化剂在碱性介质下的3级和2级电解体系的全水分解性能。通过XRD和TEM/EDX等不同的物理表征表明,两种材料(Nd2Se3和Mn2O3)的强结合导致了前驱体的结构重构和球形形成,无序孔隙和活性位点数量增加。此外,XPS证实了强电子耦合,与纯氢相比,增强了氢原子在催化剂表面的吸附。在10 mA cm−2时,Nd2Se3 - Mn2O3对OER和HER的过电位最小,分别为260和121 mV,表明Nd2Se3和Mn2O3的耦合作用是提高催化性能的原因。用EIS和Cdl证实了小电荷转移电阻和大表面积对双功能电催化剂HER-OER的影响。此外,在双电极电解槽中组装的Nd2Se3-Mn2O3 // Nd2Se3-Mn2O3器件的电池电压为1.47 V,在10 mA cm−2下具有96 h的优异稳定性。本研究为通过异质结调节双功能催化剂的界面效应,开发高效、耐用的电催化剂铺平了道路。
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来源期刊
International Journal of Hydrogen Energy
International Journal of Hydrogen Energy 工程技术-环境科学
CiteScore
13.50
自引率
25.00%
发文量
3502
审稿时长
60 days
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.
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