Enhanced Stability and Catalytic Performance of Active Rh Sites on Al2O3 Via Atomic Layer Deposited ZrO2

被引:10
作者
Guo, Feng [1 ,2 ]
Li, Jingwei [3 ]
Zhang, Yibo [2 ,4 ,5 ]
Yang, Xiangguang [2 ,4 ,5 ]
机构
[1] Nanchang Univ, Dept Chem, Nanchang 330031, Peoples R China
[2] Chinese Acad Sci, Ganjiang Innovat Acad, Jiangxi Inst Rare Earths, Ganzhou 341000, Peoples R China
[3] Shanxi Datong Univ, Coll Chem & Chem Engn, Datong 037009, Peoples R China
[4] Chinese Acad Sci, Changchun Inst Appl Chem, Jilin Prov Key Lab Green Chem & Proc, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[5] Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
NO-CO REACTION; DISPERSED RH; RHODIUM; REDUCTION; EMISSIONS; OXIDATION; RH/AL2O3; STEAM; DEACTIVATION; PASSIVATION;
D O I
10.1021/acs.jpclett.2c02219
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Modulating the Rh active sites on surfaces of Al2O3 is crucial to developing effective three-way catalysts. Herein, an ultralow amount of ZrO2 (0.0179%) was deposited onto Al2O3 nanorods via atomic layer deposition (ALD) to form a catalyst with both thermal stability and low-temperature activity. The results demonstrate that the ALD-ZrO2 is conducive to improve the catalytic activity of the Rh site and inhibit the formation of irreducible Rh species at high temperature. The obtained catalysts show satisfactory performance for a model NO-CO reaction even after thermal aging at 1050 degrees C. This strategy shows that a molecularly precise synthesis can lead to the robust promotion of Rh activity under low temperature and provide a promising path toward reducing the deactivation of catalysts at high temperature.
引用
收藏
页码:8825 / 8832
页数:8
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