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用于高效电催化尿素氧化的分级结构MnO@NiCo-LDH纳米阵列的可控制备

Controlled Fabrication of Hierarchically Structured MnO@NiCo-LDH Nanoarrays for Efficient Electrocatalytic Urea Oxidization.

作者信息

Liu Wenjun, Xu Wenbo, Dong Guofa, Fang Ming

机构信息

Shenzhen Key Laboratory of Special Functional Materials, Guangdong Research Centre for Interfacial Engineering of Functional Materials, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518060, China.

Fujian Key Laboratory of Functional Marine Sensing Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, China.

出版信息

Nanomaterials (Basel). 2023 Aug 7;13(15):2268. doi: 10.3390/nano13152268.

Abstract

Urea, a prevalent component found in wastewater, shows great promise as a substrate for energy-efficient hydrogen production by electrolysis. However, the slow kinetics of the anodic urea oxidation reaction (UOR) significantly hamper the overall reaction rate. This study presents the design and controlled fabrication of hierarchically structured nanomaterials as potential catalysts for UOR. The prepared MnO@NiCo-LDH hybrid catalyst demonstrates remarkable improvements in reaction kinetics, benefiting from synergistic enhancements in charge transfer and efficient mass transport facilitated by its unique hierarchical architecture. Notably, the catalyst exhibits an exceptionally low onset potential of 1.228 V and requires only 1.326 V to achieve an impressive current density of 100 mA cm, representing a state-of-the-art performance in UORs. These findings highlight the tremendous potential of this innovative material designing strategy to drive advancements in electrocatalytic processes.

摘要

尿素是废水中常见的成分,作为通过电解进行节能制氢的底物具有很大潜力。然而,阳极尿素氧化反应(UOR)缓慢的动力学显著阻碍了整体反应速率。本研究展示了分层结构纳米材料作为UOR潜在催化剂的设计与可控制备。制备的MnO@NiCo-LDH复合催化剂在反应动力学方面有显著改善,这得益于其独特分层结构促进的电荷转移协同增强和高效传质。值得注意的是,该催化剂具有1.228 V的极低起始电位,仅需1.326 V就能实现100 mA cm的可观电流密度,代表了UOR中的先进性能。这些发现突出了这种创新材料设计策略在推动电催化过程进步方面的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0120/10421065/8fe1cfd26208/nanomaterials-13-02268-g001.jpg

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