检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:WANG Ke ZHANG Rui WANG Huilin ZHANG Lingling WANG Zijian WANG Xiao SONG Shuyan ZHANG Hongjie
机构地区:[1]State Key Laboratory of Rare Earth Resource Utilization,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun 130022,P.R.China [2]School of Applied Chemistry and Engineering,University of Science and Technology of China,Hefei 230026,P.R.China [3]Department of Chemistry,Tsinghua University,Beijing 100084,P.R.China
出 处:《Chemical Research in Chinese Universities》2024年第6期970-977,共8页高等学校化学研究(英文版)
基 金:supported by the National Science and Technology Major Project of China(No.2021YFB3500700);the National Natural Science Foundation of China(Nos.22020102003,22025506,22271274);the Program of Science and Technology Development Plan of Jilin Province,China(Nos.20230101035JC,20230101022JC).
摘 要:Establishing efficient CO_(2) hydrogenation technology based on the reverse water-gas shift (RWGS) reaction can effectively alleviate environmental problems while providing high-value-added products.The development of suitable advanced supports is the key to improving the catalytic activity and selectivity.Herein,we designed and synthesized a new type of spinel-phase high entropy oxides [(FeCrMnAlGa)3O4-x,FMG],which exhibited remarkable RWGS performance after loading small-size Rh nanoparticles.The CO yield was as high as 145.5 μmolCO·gcat^(-1)·s^(-1) at 380 ℃ and the CO selectivity was nearly 100%.Moreover,the catalyst retained over 95% of the initial activity after 25 h of continuous catalyzing.Experimental and structural studies reveal that the FMG support has elemental synergy and high-entropy stability,which affect the Rh dispersion and oxygen vacancy generation,in turn achieving superior catalytic performance.
关 键 词:High entropy oxide(HEO) Reverse water-gas shift(RWGS) Size effect Elemental synergy
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:3.129.211.72