Long Yunpeng, Zhu Xiao, Gao Chuan, Si Wenzhe, Li Junhua, Peng Yue
School of Environment, Tsinghua University, Beijing, 100084, P. R. China.
Nat Commun. 2025 Jan 26;16(1):1048. doi: 10.1038/s41467-025-56487-5.
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.
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。