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从环保型微生物菌体制备的原子分散铁位点作为高效加氢催化剂。

Atomically dispersed iron sites from eco-friendly microbial mycelium as highly efficient hydrogenation catalyst.

机构信息

College of Energy, College of Chemistry and Chemical Engineering, College of Materials, Xiamen University, Xiamen 361102, Fujian, China.

College of Energy, College of Chemistry and Chemical Engineering, College of Materials, Xiamen University, Xiamen 361102, Fujian, China.

出版信息

J Colloid Interface Sci. 2025 Feb;679(Pt A):824-833. doi: 10.1016/j.jcis.2024.09.250. Epub 2024 Oct 9.

DOI:10.1016/j.jcis.2024.09.250
PMID:39395221
Abstract

Iron, one of the most abundant elements on earth and an essential element for living organisms, plays a crucial role in our daily metabolism. In the field of catalysis, the development of high-performance catalysts based on less toxic iron element is also of significant importance for green chemistry and a sustainable future. To construct Fe-based heterogeneous catalysts with excellent hydrogenation performance, precise modulation of the atomic coordination structure is a key strategy for enhancing catalytic activity. In this study, we present an in-situ coating method for applying a zeolitic imidazolate framework (ZIF) onto the surface of fungal hyphae. The asymmetric coordination structure of Fe-NP was precisely tailored by utilizing the phosphorus source from the fungus and the nitrogen source in the ZIFs. Detailed characterizations and density functional theory calculations revealed that the incorporation of ZIFs not only increased the specific surface area of catalysts, but also facilitated the dispersion of FeP nanoparticles into the Fe-NP center, making the lowest reaction energy barrier and resulting in the best performance for nitrobenzene hydrogenation when compared to the FeP nanoparticles and clusters. This research introduces a novel design concept for constructing asymmetric monoatomic configuration based on the inherent characteristics of natural microorganisms and the exogenous porous coordination polymers.

摘要

铁是地球上最丰富的元素之一,也是生物生存所必需的元素,在我们的日常代谢中起着至关重要的作用。在催化领域,开发基于毒性较低的铁元素的高性能催化剂对于绿色化学和可持续的未来也非常重要。为了构建具有优异加氢性能的基于铁的多相催化剂,精确调控原子配位结构是提高催化活性的关键策略。在这项研究中,我们提出了一种原位涂层方法,即将沸石咪唑酯骨架(ZIF)应用于真菌菌丝体的表面。利用真菌中的磷源和 ZIF 中的氮源,精确地调整了 Fe-NP 的不对称配位结构。详细的表征和密度泛函理论计算表明,ZIF 的引入不仅增加了催化剂的比表面积,而且还促进了 FeP 纳米颗粒分散到 Fe-NP 中心,使得硝基苯加氢的最低反应能垒最低,性能最佳,与 FeP 纳米颗粒和团簇相比。这项研究为构建基于天然微生物固有特性和外部分孔配位聚合物的不对称单原子构型引入了一种新的设计概念。

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