Regulating the Spin State of Single Noble Metal Atoms by Hydroxyl for Selective Dehydrogenation of CH 4 Direct Conversion to CH 3 OH.

The key scientific challenge for methane (CH 4 ) direct conversion to methanol (CH 3 OH) is considered to be the prevention of overoxidation of target products, which is restrained by the difficulty in the well-controlled process of selective dehydrogenation. Herein, we take single noble metal atom-anchored hexagonal boron nitride nanosheets with B vacancies (M SA /B 1- x N) as the model materials and first propose that the dehydrogenation in the direct conversion of CH 4 to CH 3 OH is highly dependent on the spin state of the noble metal. The results reveal that the noble metal with a higher spin magnetic moment is beneficial to the formation of the spin channels for electron transfer, which boosts the dissociation of C-H bonds. The promoted process of dehydrogenation will lead not only to the effective activation of CH 4 but also to the easy overoxidation of CH 3 OH. More importantly, it is found that the spin state of noble metals can be regulated by the introduction of hydroxyl (OH), which realizes the selective dehydrogenation in the process of CH 4 direct conversion to CH 3 OH. Among them, Ag SA /B 1- x N exhibits the best performance owing to the dynamic regulation spin state of a single Ag atom by OH. On the one hand, the introduction of OH significantly reduces the energy barrier of C-H bond dissociation by the increase in the spin magnetic moment. On the other hand, the high spin magnetic moment of a single Ag atom during the process of subsequent dehydrogenation can be modulated to nearly zero. As a result, the spin channel for electron transfer between the adsorbed CH 3 OH and reactive sites is broken, which hinders its overoxidation. This work opens a new path to designing catalysts for selective dehydrogenation by tuning the spin state of local electronic structures.