Tae Hwan Lim , Su Bin Park , Ji Man Kim , Do Heui Kim
{"title":"有序介孔MCo2O4 (M = Cu, Zn和Ni)尖晶石催化剂具有较高的甲烷燃烧催化性能","authors":"Tae Hwan Lim , Su Bin Park , Ji Man Kim , Do Heui Kim","doi":"10.1016/j.molcata.2016.11.002","DOIUrl":null,"url":null,"abstract":"<div><p>Ordered mesoporous MCo<sub>2</sub>O<sub>4</sub> (M<!--> <!-->=<!--> <!-->Cu, Zn and Ni) spinel catalysts were synthesized via nano-replication method using mesoporous silica KIT-6 as the hard template. They were applied to methane combustion, in comparison with bulk MCo<sub>2</sub>O<sub>4</sub> spinel catalysts prepared by co-precipitation method. A combined N<sub>2</sub> adsorption-desorption, XRD and TEM results clearly confirm that mesoporous MCo<sub>2</sub>O<sub>4</sub> (m-MCo<sub>2</sub>O<sub>4</sub>) spinel catalysts contain ordered mesostructure, resulting in the higher BET surface area and pore volume than bulk ones (b-MCo<sub>2</sub>O<sub>4</sub>). Moreover, the former catalysts demonstrate the better thermal stability as indicated by larger amount of MCo<sub>2</sub>O<sub>4</sub> phase and smaller size of crystallite domain after calcination at 550<!--> <!-->°C. Therefore, such excellent properties rationalize that the m-MCo<sub>2</sub>O<sub>4</sub> spinel catalysts reveal higher catalytic activity for methane combustion than bulk counterparts. When it comes to the catalytic performance of the meso catalysts for methane combustion, the m-CuCo<sub>2</sub>O<sub>4</sub> spinel catalyst has superior performance, which is related to the high normalized amount of Co<sup>3+</sup> cations on the surface, as evidenced by XPS.</p></div>","PeriodicalId":370,"journal":{"name":"Journal of Molecular Catalysis A: Chemical","volume":"426 ","pages":"Pages 68-74"},"PeriodicalIF":5.0620,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.molcata.2016.11.002","citationCount":"42","resultStr":"{\"title\":\"Ordered mesoporous MCo2O4 (M = Cu, Zn and Ni) spinel catalysts with high catalytic performance for methane combustion\",\"authors\":\"Tae Hwan Lim , Su Bin Park , Ji Man Kim , Do Heui Kim\",\"doi\":\"10.1016/j.molcata.2016.11.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Ordered mesoporous MCo<sub>2</sub>O<sub>4</sub> (M<!--> <!-->=<!--> <!-->Cu, Zn and Ni) spinel catalysts were synthesized via nano-replication method using mesoporous silica KIT-6 as the hard template. They were applied to methane combustion, in comparison with bulk MCo<sub>2</sub>O<sub>4</sub> spinel catalysts prepared by co-precipitation method. A combined N<sub>2</sub> adsorption-desorption, XRD and TEM results clearly confirm that mesoporous MCo<sub>2</sub>O<sub>4</sub> (m-MCo<sub>2</sub>O<sub>4</sub>) spinel catalysts contain ordered mesostructure, resulting in the higher BET surface area and pore volume than bulk ones (b-MCo<sub>2</sub>O<sub>4</sub>). Moreover, the former catalysts demonstrate the better thermal stability as indicated by larger amount of MCo<sub>2</sub>O<sub>4</sub> phase and smaller size of crystallite domain after calcination at 550<!--> <!-->°C. Therefore, such excellent properties rationalize that the m-MCo<sub>2</sub>O<sub>4</sub> spinel catalysts reveal higher catalytic activity for methane combustion than bulk counterparts. When it comes to the catalytic performance of the meso catalysts for methane combustion, the m-CuCo<sub>2</sub>O<sub>4</sub> spinel catalyst has superior performance, which is related to the high normalized amount of Co<sup>3+</sup> cations on the surface, as evidenced by XPS.</p></div>\",\"PeriodicalId\":370,\"journal\":{\"name\":\"Journal of Molecular Catalysis A: Chemical\",\"volume\":\"426 \",\"pages\":\"Pages 68-74\"},\"PeriodicalIF\":5.0620,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.molcata.2016.11.002\",\"citationCount\":\"42\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Catalysis A: Chemical\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1381116916304587\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Catalysis A: Chemical","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1381116916304587","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Ordered mesoporous MCo2O4 (M = Cu, Zn and Ni) spinel catalysts with high catalytic performance for methane combustion
Ordered mesoporous MCo2O4 (M = Cu, Zn and Ni) spinel catalysts were synthesized via nano-replication method using mesoporous silica KIT-6 as the hard template. They were applied to methane combustion, in comparison with bulk MCo2O4 spinel catalysts prepared by co-precipitation method. A combined N2 adsorption-desorption, XRD and TEM results clearly confirm that mesoporous MCo2O4 (m-MCo2O4) spinel catalysts contain ordered mesostructure, resulting in the higher BET surface area and pore volume than bulk ones (b-MCo2O4). Moreover, the former catalysts demonstrate the better thermal stability as indicated by larger amount of MCo2O4 phase and smaller size of crystallite domain after calcination at 550 °C. Therefore, such excellent properties rationalize that the m-MCo2O4 spinel catalysts reveal higher catalytic activity for methane combustion than bulk counterparts. When it comes to the catalytic performance of the meso catalysts for methane combustion, the m-CuCo2O4 spinel catalyst has superior performance, which is related to the high normalized amount of Co3+ cations on the surface, as evidenced by XPS.
期刊介绍:
The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.