中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly active metal sites confined at oxide/metal interfaces for catalytic oxidation reactions

文献类型:会议论文

作者Fu Q(傅强) ; Li WX(李微雪) ; Mu RT(慕仁涛) ; Yao YX(姚云喜) ; Ma T(马腾) ; Liu HY(刘洪阳) ; Su HY(苏海燕) ; Ma D(马丁) ; Gu XK(顾向奎) ; Chen LM(陈礼敏) ; Wang Z(王珍) ; Zhang H(张辉) ; Wang B(王冰) ; Bao XH(包信和)
出版日期2011
会议名称international conference on clean energy science 2011
会议日期2011-4-10
会议地点大连
页码161-0
通讯作者包信和
中文摘要bimetallic catalysts are widely used in many heterogeneous catalytic processes. with rational design of the surface structure of the bimetallic catalysts, improved catalytic performance can be achieved in comparison to their parent metals. here, we demonstrate that the nanostructured ferrous oxides (feo) grown on pt present the best reactivity to the co oxidation among various fe-pt(111) surface structures. using surface science measurements and density functional calculations, we show that the interface confinement effect can be attributed to the stabilization of the monolayer-dispersed ferrous oxide nanoislands and coordinatively unsaturated ferrous (cuf) sites at the edges of the feo nanoislands by taking advantage of strong adhesion between the nanostructured oxides and the metal substrates. the cuf sites together with the metal supports are active for o2 activation, and the structural ensemble was highly efficient for co oxidation using both model systems and practical supported catalysts. the interface confinement effect could be extended to other oxide-metal systems as well. in pt-ni systems, we observe the formation of monolayer-dispersed nio nanoislands on pt(111) and the interface-confined coordinatively unsaturated ni atoms. the nio/pt(111) is highly active for co oxidation as well.
合作状况墙报
会议主办者大连化物所
会议录abstract book
会议录出版者待补充
学科主题物理化学
会议录出版地待补充
源URL[http://159.226.238.44/handle/321008/116123]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
推荐引用方式
GB/T 7714
Fu Q,Li WX,Mu RT,et al. Highly active metal sites confined at oxide/metal interfaces for catalytic oxidation reactions[C]. 见:international conference on clean energy science 2011. 大连. 2011-4-10.

入库方式: OAI收割

来源:大连化学物理研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。