Robust 2 nm-sized gold nanoclusters on Co3O4 for CO oxidation

被引:6
作者
Shi, Quanquan [1 ,5 ,6 ]
Li, Zhiwen [2 ,4 ]
Cao, Changhai [3 ]
Li, Gao [2 ,4 ]
Barkaoui, Sami [2 ]
机构
[1] Inner Mongolia Agr Univ, Coll Sci, Hohhot 010018, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] SINOPEC Dalian Res Inst Petr & Petrochem Co Ltd, Key Lab Biofuels & Biochem Engn, Dalian 116045, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Inner Mongolia Key Lab Soil Qual & Nutrient Reso, Hohhot 010018, Peoples R China
[6] Key Lab Agr Ecol Secur & Green Dev Univ Inner Mon, Hohhot 010018, Peoples R China
来源
NANOSCALE ADVANCES | 2023年 / 5卷 / 19期
基金
中国国家自然科学基金;
关键词
ACTIVE GOLD; CATALYSTS; TIO2;
D O I
10.1039/d3na00561e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, gold nanoparticles were dispersed on Co3O4 nanoplates, forming a specific Au-Co3O4 interface. Upon calcination at 300 degrees C in air, aberration-corrected STEM images evidenced that the gold nanoclusters (NCs) on Co3O4{111} were maintained at ca. 2.2 nm, which is similar to the size of the parent Au colloidal particles, demonstrating the stronger metal-support interaction (SMSI) on Co3O4{111}. Au/Co3O4{111} showed good catalytic activity (a full CO conversion achieved at 80 degrees C) and durability (over 10 hours) in CO oxidation, which was mainly due to the promotion by the surface oxygen vacancies and intrinsic defects of Co3O4{111} for activating O-2 and by Au-0, Au delta+, and Au+ species on the surface of gold NCs for CO activation, as evidenced by Raman and Fourier-transform infrared (FT-IR) spectroscopy analysis. Au/Co3O4 catalyzed CO oxidation obeyed the Langmuir-Hinshelwood mechanism at low temperatures.
引用
收藏
页码:5385 / 5389
页数:5
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