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Si, Yang; Jiao, Yueyue; Wang, Maolin; Xiang, Shengling; Diao, Jiangyong; Chen, Xiaowen; Chen, Jiawei; Wang, Yue; Xiao, Dequan; Wen, Xiaodong; Wang, Ning; Ma, Ding; Liu, Hongyang
Nature communications, 06/2024, Volume: 15, Issue: 1Journal Article
Abstract For di-nitroaromatics hydrogenation, it is a challenge to achieve the multi-step hydrogenation with high activity and selectivity due to the complexity of the process involving two nitro groups. Consequently, many precious metal catalysts suffer from low activity for this multi-step hydrogenation reaction. Herein, we employ a fully exposed Pt clusters catalyst consisting of an average of four Pt atoms on nanodiamond@graphene (Pt n /ND@G), demonstrating excellent catalytic performance for the multi-step hydrogenation of 2,4-dinitrotoluene. The TOF (40647 h −1 ) of Pt n /ND@G is significantly superior to that of single Pt atoms catalyst, Pt nanoparticles catalyst, and even all the known catalysts. Density functional theory calculations and absorption experiments reveal that the synergetic interaction between the multiple active sites of Pt n /ND@G facilitate the co-adsorption/activation of reactants and H 2 , as well as the desorption of intermediates/products, which is the key for the higher catalytic activity than single Pt atoms catalyst and Pt nanoparticles catalyst.
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