Suppr超能文献

ZIF-67 衍生的 NiCo 层状双氢氧化物@中空纳米笼结构碳纳米管作为增强型电催化剂用于乙醇氧化反应。

ZIF-67-Derived NiCo-Layered Double Hydroxide@Carbon Nanotube Architectures with Hollow Nanocage Structures as Enhanced Electrocatalysts for Ethanol Oxidation Reaction.

机构信息

College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004, China.

Key Laboratory of New Technology for Processing Nonferrous Metals and Materials, Ministry of Education, Collaborative Innovation Center for Exploration of Nonferrous Metal Deposits and Efficient Utilization of Resources in Guangxi, Guilin University of Technology, Guilin 541004, China.

出版信息

Molecules. 2023 Jan 25;28(3):1173. doi: 10.3390/molecules28031173.

Abstract

The rational design of efficient Earth-abundant electrocatalysts for the ethanol oxidation reaction (EOR) is the key to developing direct ethanol fuel cells (DEFCs). Among these, the smart structure is highly demanded for highly efficient and stable non-precious electrocatalysts based on transition metals (such as Ni, Co, and Fe). In this work, high-performance NiCo-layered double hydroxide@carbon nanotube (NiCo-LDH@CNT) architectures with hollow nanocage structures as electrocatalysts for EOR were prepared via sacrificial ZIF-67 templates on CNTs. Comprehensive structural characterizations revealed that the as-synthesized NiCo-LDH@CNTs architecture displayed 3D hollow nanocages of NiCo-LDH and abundant interfacial structure between NiCo-LDH and CNTs, which could not only completely expose active sites by increasing the surface area but also facilitate the electron transfer during the electrocatalytic process, thus, improving EOR activity. Benefiting from the 3D hollow nanocages and interfacial structure fabricated by the sacrificial ZIF-67-templated method, the NiCo-LDH@CNTs-2.5% architecture exhibited enhanced electrocatalytic activity for ethanol oxidation compared to single-component NiCo-LDH, where the peak current density was 11.5 mA·cm, and the j/j value representing the resistance to catalyst poisoning was 1.72 in an alkaline environment. These results provide a new perspective on the fabrication of non-precious metal electrocatalysts for EOR in DEFCs.

摘要

高效的乙醇氧化反应 (EOR) 电催化剂的合理设计是开发直接乙醇燃料电池 (DEFC) 的关键。在这些电催化剂中,基于过渡金属(如 Ni、Co 和 Fe)的高效和稳定的非贵金属电催化剂非常需要智能结构。在这项工作中,通过牺牲 ZIF-67 模板在 CNTs 上制备了高性能的 NiCo 层状双氢氧化物@碳纳米管 (NiCo-LDH@CNT) 作为 EOR 电催化剂的具有空心纳米笼结构的架构。综合结构表征表明,所合成的 NiCo-LDH@CNTs 结构显示出 3D 空心纳米笼的 NiCo-LDH 和 NiCo-LDH 与 CNTs 之间丰富的界面结构,这不仅可以通过增加表面积来完全暴露活性位点,而且可以促进电催化过程中的电子转移,从而提高 EOR 活性。受益于牺牲 ZIF-67 模板法制备的 3D 空心纳米笼和界面结构,NiCo-LDH@CNTs-2.5% 结构在碱性环境下表现出比单一组分 NiCo-LDH 更高的乙醇氧化电催化活性,其峰值电流密度为 11.5 mA·cm,代表催化剂中毒阻力的 j/j 值为 1.72。这些结果为在 DEFC 中制备 EOR 的非贵金属电催化剂提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e81f/9920546/43a8367a5945/molecules-28-01173-sch001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验