Ultrasonication-Induced Strong Metal-Support Interaction Construction in Water Towards Enhanced Catalysis

被引:29
作者
Siniard, Kevin M. [1 ]
Li, Meijia [2 ]
Yang, Shi-Ze [3 ]
Zhang, Junyan [2 ]
Polo-Garzon, Felipe [2 ]
Wu, Zili [2 ]
Yang, Zhenzhen [2 ]
Dai, Sheng [1 ,2 ]
机构
[1] Univ Tennessee, Inst Adv Mat & Mfg, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37831 USA
[3] Arizona State Univ, Eyring Mat Ctr, Tempe, AZ 85287 USA
关键词
CO2; Conversion; Encapsulation; Hydrogenation; Strong Metal-Support Interactions; Ultrasonication; HETEROGENEOUS CATALYSTS; OXYGEN VACANCIES; TIO2; SURFACE; OXIDE; ADSORPTION; TITANIUM; NANOPARTICLES; OVERLAYERS; REDUCTION;
D O I
10.1002/anie.202214322
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of facile methodologies to afford robust supported metal nanocatalysts under mild conditions is highly desirable yet challenging, particularly via strong metal-support interactions (SMSI) construction. State-of-the-art approaches capable of generating SMSI encapsulation mainly focus on high temperature annealing in reductive/oxidative atmosphere. Herein, ultra-stable metal nanocatalysts based on SMSI construction were produced by leveraging the instantaneous high-energy input from ultrasonication under ambient conditions in H2O, which could rapidly afford abundant active intermediates, Ti3+ ions, and oxygen vacancies within the scaffolds to induce the SMSI overlayer formation. The encapsulation degree could be tuned and controlled via the reducibility of the solvents and the ultrasonication parameters. This facile and efficient approach could be further extended to diverse metal oxide supports and noble metal NPs leading to enhanced performance in hydrogenation reactions and CO2 conversion.
引用
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页数:8
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