文摘
The synthesis of atomically thin transition-metal oxide nanosheets as a conceptually new class of materials is significant for the development of next-generation electronic and magnetic nanodevices but remains a fundamental chemical and physical challenge. Here, based on a 鈥渢emplate-assisted oriented growth鈥?strategy, we successfully synthesized half-unit-cell nanosheets of a typical transition-metal oxide 伪-Fe2O3 that show robust intrinsic ferromagnetism of 0.6 渭B/atom at 100 K and remain ferromagnetic at room temperature. A unique surface structure distortion, as revealed by X-ray absorption spectroscopy, produces nonidentical Fe ion environments and induces distance fluctuation of Fe ion chains. First-principles calculations reveal that the efficient breaking of the quantum degeneracy of Fe 3d energy states activates ferromagnetic exchange interaction in these Fe5-co鈥揙鈥揊e6-co ion chains. These results provide a solid design principle for tailoring the spin-exchange interactions and offer promise for future semiconductor spintronics.