催化作用
烧结
纳米材料基催化剂
材料科学
化学工程
壳体(结构)
降级(电信)
结块
纳米技术
化学
冶金
复合材料
有机化学
计算机科学
电信
工程类
作者
Seung‐Hyun Kim,Siwon Lee,WooChul Jung
出处
期刊:Chemcatchem
[Wiley]
日期:2019-07-16
卷期号:11 (18): 4653-4659
被引量:25
标识
DOI:10.1002/cctc.201900934
摘要
Abstract Although core‐shell catalysts have been actively studied for their excellent stability at high temperatures, most studies have focused on the development of synthetic methods and not conducted actual catalytic reactions at conditions, under which particles severely agglomerate. Here, we prepare a model catalyst with a well‐defined size and interface of a Pt core and a gas‐permeable SiO 2 shell via advanced colloidal synthesis, and evaluate the catalytic response to CO and CH 4 oxidation, each representing low (<300 °C) and high (>500 °C) temperature reactions. Compared to typical SiO 2 supported Pt, the core‐shell configuration shows comparable activity at CO oxidation and a much higher activity and stability for CH 4 oxidation. However, even for the core‐shell, degradation is inevitable, and possible reasons for this are discussed. These practical results on high‐temperature catalysis provide important evaluation criteria and design guidelines for sintering‐resistant nanocatalysts.
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