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用于一氧化碳氧化和一氧化氮分解的氧化钴晶体-非晶界面处钴自旋态的调制

Modulation of Co spin state at CoO crystalline-amorphous interfaces for CO oxidation and NO decomposition.

作者信息

Long Yunpeng, Zhu Xiao, Gao Chuan, Si Wenzhe, Li Junhua, Peng Yue

机构信息

School of Environment, Tsinghua University, Beijing, 100084, P. R. China.

出版信息

Nat Commun. 2025 Jan 26;16(1):1048. doi: 10.1038/s41467-025-56487-5.

Abstract

Modulation of electronic spin states in cobalt-based catalysts is an effective strategy for molecule activations. Crystalline-amorphous interfaces often exhibit unique catalytic properties due to disruptions of long-range order and alterations in electronic structure. However, the mechanisms of molecule activation and spin states at interfaces remain elusive. Herein, we present a CoO spinel-based catalyst featuring crystalline-amorphous interfaces. Characterization analyses confirm that tetrahedral Co is selectively etched from bulk spinel, forming amorphous CoO islands on the surface. The resultant symmetry breaking in the coordination field induces a reconstruction of the Co 3 d orbitals, leading to high-spin states. In CO oxidation, the interface serves as novel active sites with a lower energy barrier, facilitated by lattice oxygen activation. In NO decomposition, the interface promotes reassociation of dissociated oxygen through quantum spin exchange interactions. This work provides a straightforward approach to modulating the spin state of interfaces and elucidates their role in molecule activations.

摘要

调节钴基催化剂中的电子自旋态是激活分子的有效策略。由于长程有序性的破坏和电子结构的改变,晶态-非晶态界面通常表现出独特的催化性能。然而,界面处分子激活和自旋态的机制仍然难以捉摸。在此,我们展示了一种具有晶态-非晶态界面的CoO尖晶石基催化剂。表征分析证实,四面体Co从块状尖晶石中被选择性蚀刻,在表面形成非晶态CoO岛。配位场中由此产生的对称性破缺诱导了Co 3d轨道的重构,导致高自旋态。在CO氧化反应中,该界面作为具有较低能垒的新型活性位点,通过晶格氧的活化得以促进。在NO分解反应中,该界面通过量子自旋交换相互作用促进解离氧的重新结合。这项工作提供了一种调节界面自旋态的直接方法,并阐明了它们在分子激活中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/11770148/f8606c6d90b7/41467_2025_56487_Fig1_HTML.jpg

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