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将含钌高熵硫化物结构重构为高效碱性析氧催化剂。

Structural reconfiguration of an Ru-bearing high-entropy sulfide into an efficient alkaline oxygen evolution catalyst.

作者信息

Peng Wenfeng, Lv Zhengxing, Cheng Wenbo, Li Jiong, Zhao Shijing, Yan Bingmin, Shang Lu, Zhou Junshuang, Zhang Tierui, Gou Huiyang

机构信息

College of Energy Engineering, Huanghuai University, Zhumadian 463000, China.

Center for High Pressure Science and Technology Advanced Research, Beijing 100193, China.

出版信息

Chem Commun (Camb). 2025 May 13;61(40):7261-7264. doi: 10.1039/d5cc00974j.

Abstract

High-entropy sulfides (HESs) with multiple metals are one of the most promising electrocatalysts, but the ambiguous self-reconstruction mechanism greatly hinders their further practical applications in water electrolysis. Here, an Ru-bearing high-entropy sulfide (FeCoNiCuRu)S was prepared by employing a facile high-pressure and high-temperature (HPHT) method. The obtained high-entropy sulfide (FeCoNiCuRu)S exhibited excellent OER performance and robust stability in a 1 M KOH solution. By employing X-ray absorption spectroscopy (XAS) and Raman spectroscopy, along with TEM and XPS characterization, we determine the specific self-reconstruction path (MS was directly converted into MOOH) and real active species. This research offers great opportunities for the development of highly efficient catalysts.

摘要

含多种金属的高熵硫化物(HESs)是最具前景的电催化剂之一,但模糊的自重构机制极大地阻碍了它们在水电解中的进一步实际应用。在此,通过简便的高压高温(HPHT)方法制备了一种含钌的高熵硫化物(FeCoNiCuRu)S。所制备的高熵硫化物(FeCoNiCuRu)S在1 M KOH溶液中表现出优异的析氧反应(OER)性能和稳健的稳定性。通过采用X射线吸收光谱(XAS)、拉曼光谱以及透射电子显微镜(TEM)和X射线光电子能谱(XPS)表征,我们确定了具体的自重构路径(MS直接转化为MOOH)和实际活性物种。该研究为高效催化剂的开发提供了巨大机遇。

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