Li Zhijun, Li Honghong, Yang Zening, Lu Xiaowen, Ji Siqi, Zhang Mingyang, Horton J Hugh, Ding Honghe, Xu Qian, Zhu Junfa, Yu Jin
Joint International Research Laboratory of Advanced Chemical Catalytic Materials and Surface Science, College of Chemistry and Chemical Engineering, Northeast Petroleum University, Daqing, 163318, P. R. China.
School of Materials Science and Engineering, Jiangsu Province Key Laboratory of Advanced Metallic Materials, Southeast University, Nanjing, 211189, P. R. China.
Small. 2022 May;18(19):e2201092. doi: 10.1002/smll.202201092. Epub 2022 Apr 10.
The facile creation of high-performance single-atom catalysts (SACs) is intriguing in heterogeneous catalysis, especially on 2D transition-metal dichalcogenides. An efficient spontaneous reduction approach to access atomically dispersed iron atoms supported over defect-containing MoS nanosheets is herein reported. Advanced characterization methods demonstrate that the isolated iron atoms situate atop of molybdenum atoms and coordinate with three neighboring sulfur atoms. This Fe SAC delivers exceptional catalytic efficiency (1 atm O @ 120 °C) in the selective oxidation of benzyl alcohol to benzaldehyde, with 99% selectivity under almost 100% conversion. The turnover frequency is calculated to be as high as 2105 h . Moreover, it shows admirable recyclability, storage stability, and substrate tolerance. Density functional theory calculations reveal that the high catalytic activity stems from the optimized electronic structure of single iron atoms over the MoS support.
在多相催化中,尤其是在二维过渡金属二硫属化物上,轻松制备高性能单原子催化剂(SAC)颇具吸引力。本文报道了一种有效的自发还原方法,用于制备负载在含缺陷的MoS纳米片上的原子分散铁原子。先进的表征方法表明,孤立的铁原子位于钼原子之上,并与三个相邻的硫原子配位。这种铁单原子催化剂在苄醇选择性氧化为苯甲醛反应中表现出卓越的催化效率(1个大气压氧气,120°C),在几乎100%转化率下选择性达99%。计算得出的周转频率高达2105 h⁻¹。此外,它还具有出色的可回收性、储存稳定性和底物耐受性。密度泛函理论计算表明,高催化活性源于MoS载体上单个铁原子的电子结构优化。