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基于ZIF-67@酵母构建增强Co-N-C单原子催化剂共负载的工程策略

Engineering Strategy for Enhancing the Co Loading of Co-N-C Single-Atomic Catalysts Based on the ZIF-67@Yeast Construction.

作者信息

Wu Shuo, Xu Xiaolong, Wang Zelin, Ke Xiaoxing, Gu Shaonan, Zhou Guowei, Wang Lianzhou

机构信息

Key Laboratory of Fine Chemicals in Universities of Shandong, Jinan Engineering Laboratory for Multi-Scale Functional Materials, School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.

School of Materials Science and Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.

出版信息

ACS Appl Mater Interfaces. 2023 Aug 30;15(34):40451-40458. doi: 10.1021/acsami.3c06886. Epub 2023 Aug 15.

Abstract

The Co-N-C single-atom catalysts (SACs) have attracted great research interest in the energy storage and conversion fields owing to 100% atom utilization. However, enhancing the Co loading for higher electrocatalytic performance is still challenging. In this context, we propose an engineering strategy to fabricate the high Co atomic loading Co-N-C SACs based on the zeolitic imidazolate framework-67 (ZIF-67)@yeast construction. The rich amino groups provide the possibility for Co ion anchorage and ZIF-67@yeast construction via the biomineralization of yeast cells. The functional design induces the formation of Co-N-C sites and regulates the porosity for exposure of such Co-N-C sites. As a result, the Co-N-C sites were anchored on spherical micrometer flower carbonaceous materials through our novel strategy. The as-obtained optimal sample exhibited a Co atomic loading of 12.18 wt % and a specific surface area of 403.26 m g. High Co atomic loading and large specific surface area delivered excellent electrocatalytic kinetics as well as a high discharge voltage of 1.08 V at 10 mA cm for more than 100 h in Zn-air batteries. This work represents a promising strategy for fabricating high-loading SACs with high activity and good durability.

摘要

由于具有100%的原子利用率,氮掺杂碳负载钴单原子催化剂(SACs)在储能和转换领域引起了极大的研究兴趣。然而,提高钴负载量以获得更高的电催化性能仍然具有挑战性。在此背景下,我们提出了一种基于沸石咪唑酯骨架-67(ZIF-67)@酵母结构制备高钴原子负载量的Co-N-C SACs的工程策略。丰富的氨基通过酵母细胞的生物矿化作用为钴离子锚固和ZIF-67@酵母结构提供了可能性。功能设计诱导了Co-N-C位点的形成,并调节了孔隙率以暴露此类Co-N-C位点。结果,通过我们的新策略,Co-N-C位点被锚定在球形微米级花状碳质材料上。所获得的最佳样品表现出12.18 wt%的钴原子负载量和403.26 m²/g的比表面积。高钴原子负载量和大比表面积赋予了优异的电催化动力学,以及在锌空气电池中10 mA/cm²下超过100小时的1.08 V高放电电压。这项工作代表了一种制备具有高活性和良好耐久性的高负载量SACs的有前景的策略。

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