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用于增强碱性海水中全解水的花状Ru-CoVO-P多金属催化剂的低温磷化合成

Low-temperature phosphidation synthesis of flower-like Ru-CoVO-P polymetallic catalyst for enhanced overall water splitting in alkaline seawater.

作者信息

Tian Yongqi, Yang Yufang, Zhong Dongyan, Zhang Shuangshuang, Zhang Boyao, Li Xin, Zhou Huiya, Zhao Rong-Da, Miao Lihua

机构信息

School of Materials Science and Engineering, Liaoning University of Technology Jinzhou 121001 P. R. China

School of Medical Information Engineering, Shenyang Medical College Shenyang Liaoning 110043 P. R. China

出版信息

RSC Adv. 2025 Sep 10;15(39):32732-32745. doi: 10.1039/d5ra04957a. eCollection 2025 Sep 5.

Abstract

Developing efficient and stable bifunctional electrocatalysts for overall water splitting, especially in practical electrolytes such as seawater, remains a significant challenge in the field of energy conversion. Herein, we report the successful synthesis of a three-dimensional, flower-like polymetallic phosphide electrocatalyst (Ru-CoVO-P), constructed from self-assembled ultrathin nanosheets, a facile hydrothermal method combined with a low-temperature phosphidation strategy. The catalyst exhibits excellent bifunctional activity in 1 M KOH, requiring overpotentials of only 88.7 mV (HER) and 248.3 mV (OER) to achieve 10 mA cm. After 240 hours of cycling in a two-electrode system, a cell voltage of only 1.753 V is required to achieve a current density of 50 mA cm. More importantly, the catalyst maintains excellent performance in 1 M KOH containing seawater, demonstrating outstanding stability and great application potential. The superior performance stems from the electronic structure modulation among the polymetallic components, as well as the abundant active sites and efficient mass transport capabilities provided by the hierarchical structure. This work provides a facile and effective synthesis strategy for developing advanced polymetallic phosphide catalysts suitable for practical seawater electrolysis.

摘要

开发高效稳定的双功能电催化剂用于全水分解,尤其是在诸如海水等实际电解质中,仍然是能量转换领域的一项重大挑战。在此,我们报告了一种三维花状多金属磷化物电催化剂(Ru-CoVO-P)的成功合成,它由自组装超薄纳米片构建而成,采用了简便的水热法与低温磷化策略相结合的方法。该催化剂在1 M KOH中表现出优异的双功能活性,达到10 mA cm需要的过电位仅为88.7 mV(析氢反应)和248.3 mV(析氧反应)。在两电极系统中循环240小时后,仅需1.753 V的电池电压就能达到50 mA cm的电流密度。更重要的是,该催化剂在含海水的1 M KOH中保持优异性能,展现出出色的稳定性和巨大的应用潜力。其优异性能源于多金属组分之间的电子结构调制,以及分级结构提供的丰富活性位点和高效传质能力。这项工作为开发适用于实际海水电解的先进多金属磷化物催化剂提供了一种简便有效的合成策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1284/12421303/b152bdfde420/d5ra04957a-f1.jpg

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