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Dual-atom Pt heterogeneous catalyst with excellent catalytic performances for the selective hydrogenation and epoxidation

Atomically monodispersed heterogeneous catalysts with uniform active sites and high atom utilization efficiency are ideal heterogeneous catalytic materials. Designing such type of catalysts, however, remains a formidable challenge. Herein, using a wet-chemical method, we successfully achieved a meso...

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Detalles Bibliográficos
Autores principales: Tian, Shubo, Wang, Bingxue, Gong, Wanbing, He, Zizhan, Xu, Qi, Chen, Wenxing, Zhang, Qinghua, Zhu, Youqi, Yang, Jiarui, Fu, Qiang, Chen, Chun, Bu, Yuxiang, Gu, Lin, Sun, Xiaoming, Zhao, Huijun, Wang, Dingsheng, Li, Yadong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155026/
https://www.ncbi.nlm.nih.gov/pubmed/34039986
http://dx.doi.org/10.1038/s41467-021-23517-x
Descripción
Sumario:Atomically monodispersed heterogeneous catalysts with uniform active sites and high atom utilization efficiency are ideal heterogeneous catalytic materials. Designing such type of catalysts, however, remains a formidable challenge. Herein, using a wet-chemical method, we successfully achieved a mesoporous graphitic carbon nitride (mpg-C(3)N(4)) supported dual-atom Pt(2) catalyst, which exhibited excellent catalytic performance for the highly selective hydrogenation of nitrobenzene to aniline. The conversion of ˃99% is significantly superior to the corresponding values of mpg-C(3)N(4)-supported single Pt atoms and ultra-small Pt nanoparticles (~2 nm). First-principles calculations revealed that the excellent and unique catalytic performance of the Pt(2) species originates from the facile H(2) dissociation induced by the diatomic characteristics of Pt and the easy desorption of the aniline product. The produced Pt(2)/mpg-C(3)N(4) samples are versatile and can be applied in catalyzing other important reactions, such as the selective hydrogenation of benzaldehyde and the epoxidation of styrene.