通过异质结结构设计和内在活性耦合实现 CoP/CNT/Ni2P 相互促进,从而实现水分离

IF 6.7 1区 工程技术 Q2 ENERGY & FUELS
Fuel Pub Date : 2024-11-22 DOI:10.1016/j.fuel.2024.133761
Guo Yu , Jiaxiang Zhao , Songjia Hou , Haoyang Han , Qing Zhou , Zuoyi Yan , Jie Liu , Haohong Li , Huidong Zheng , Meiqing Zheng
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引用次数: 0

摘要

设计用于电解水的高稳定性和高活性双功能催化剂仍然是一项重大挑战。本研究通过多步电沉积和磷化策略,构建了具有三相异质结纳米结构的自支撑 CoP/CNT/Ni2P 双功能催化剂。X 射线衍射分析和透射电子显微镜显示 CoP/CNT/Ni2P 为三相异质结纳米结构,CoP/CNT/Ni2P 的扫描电子显微镜结果表明成功引入了碳纳米管(CNT)。X 射线光电子能谱结果表明,CoP/CNT/Ni2P 中的元素结合能发生了变化,这被认为有助于电催化反应。CNT 的加入增强了多相催化剂内部的电荷转移,最大限度地暴露了催化活性位点,从而提高了催化剂的性能。正如预期的那样,CoP/CNT/Ni2P 催化剂在氢气进化反应(10 mA cm-2 时为 61 mV)和氧气进化反应(100 mA cm-2 时为 342 mV)中都表现出很高的催化活性,此外,在 10 mA cm-2 的电流密度下还能长期稳定地工作 40 小时。由 CoP/CNT/Ni2P(+,-) 组成的电解槽只需 1.52 V 的适度工作电压就能在碱性水分离过程中达到 10 mA cm-2,因此性能优于商业催化剂 Pt/C||IrO2 和之前的报告。这项研究为开发超高活性和耐久性的水分离催化剂提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mutual promotion of CoP/CNT/Ni2P by heterojunction structural design and intrinsic activity coupling for water splitting

Mutual promotion of CoP/CNT/Ni2P by heterojunction structural design and intrinsic activity coupling for water splitting
The design of highly stable and active bifunctional catalysts for electrolytic water remains a significant challenge. In this study, self-supported CoP/CNT/Ni2P bifunctional catalysts with three-phase heterojunction nanostructures were constructed by a multi-step electrodeposition and phosphorylation strategy. X-ray diffraction analysis and transmission electron microscope showed that CoP/CNT/Ni2P was a three-phase heterojunction nanostructure, and scanning electron microscope results of CoP/CNT/Ni2P suggested the successful introduction of carbon nanotube (CNT). The X-ray photoelectron spectroscopy results indicate a shift in the elemental binding energy in CoP/CNT/Ni2P, which is believed to contribute to the electrocatalytic reaction. The incorporation of CNT enhances charge transfer within the multiphase catalyst and maximizes the exposure of catalytically active sites, achieving an increase in catalyst performance. As anticipated, the CoP/CNT/Ni2P catalyst displays high catalytic activity for both the hydrogen evolution reaction (61 mV at 10 mA cm−2) and the oxygen evolution reaction (342 mV at 100 mA cm−2), in addition to exhibiting long-term stability at a current density of 10 mA cm−2 over 40 h. The electrolyzer comprising CoP/CNT/Ni2P(+,−) necessitates a modest operating voltage of 1.52 V to attain 10 mA cm−2 during alkaline water splitting, thereby outperforming the commercial catalyst Pt/C||IrO2 and earlier reports. This study provides guidance for the development of ultra-high activity and durability catalysts for water splitting.
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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