Zhou Ke-bin, Chen Hong-de, Tian Qun, Zhu Bao-wei, Shen Di-xin, Xu Xiao-bai
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
J Environ Sci (China). 2005;17(1):19-24.
A series of oxygen-deficient perovskite-supported palladium catalysts were prepared by the "solid phase crystallization" (spc) method and investigated with XRD, TPR, TPD, TEM, XPS, BET analysis and CO oxidation. It was found that Pd/perovskite catalysts synthesized by the spc method were more active for CO oxidation than the calcined LaCo0.95 Pd0.05 O3, where Pd dispersed in the solid solution. H2-reducing treatment in the spc method could yield not only high-dispersed fine Pd particles on the perovskite surface but also oxygen-deficient structure. In these perovskite-supported Pd catalysts, oxygen vacancies adsorbed, activated and supplied oxygen to the active Pd sites, where the oxidation occurred with adsorbed CO. The high activities were due to the cooperative action of Pd and oxygen vacancies.
通过“固相结晶”(spc)法制备了一系列缺氧钙钛矿负载的钯催化剂,并采用XRD、TPR、TPD、TEM、XPS、BET分析和CO氧化对其进行了研究。结果发现,通过spc法合成的Pd/钙钛矿催化剂对CO氧化的活性高于煅烧后的LaCo0.95Pd0.05O3,其中Pd分散在固溶体中。spc法中的H2还原处理不仅能在钙钛矿表面产生高分散的细小Pd颗粒,还能产生缺氧结构。在这些钙钛矿负载的Pd催化剂中,氧空位吸附、活化并向活性Pd位点供应氧,CO在该位点与吸附的氧发生氧化反应。高活性归因于Pd和氧空位的协同作用。