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通过杂化环氧化物辅助/胶体晶体模板法形成三维有序分级多孔金属氧化物。

Formation of three-dimensional ordered hierarchically porous metal oxides via a hybridized epoxide assisted/colloidal crystal templating approach.

机构信息

Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA.

出版信息

ACS Appl Mater Interfaces. 2013 Aug 28;5(16):7786-92. doi: 10.1021/am401522n. Epub 2013 Aug 8.

Abstract

Three-dimensionally ordered hierarchically porous alumina, iron(III) oxide, yttria, and nickel oxide have been prepared through the hybridization of colloidal crystal-templating and a modified sol-gel method. Simply, highly ordered arrays of poly(methyl methacrylate) (PMMA) were infiltrated with a precursor solution of metal salt and epoxide. Calcination after solidification of the material removed the polymer template while forming the inverse replicas, simultaneously. These hierarchical structures possessing macropore windows and mesopore walls were characterized by powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and N2 adsorption/desorption techniques to probe the structural integrity. It was revealed by PXRD that the prepared 3D frameworks were single-phase polycrystalline structures with grain sizes between 5 and 27 nm. The thermal stability as studied by TGA illustrates expected weight losses and full decomposition of the PMMA template. SEM reveals the bimodal, hierarchical macroporous frameworks with well-defined macropore windows and mesoporous walls. Gas sorption measurements of the ordered materials display surface areas as high as 93 m(2) g(-1), and average mesopore diameter up to 33 nm. Due to the versatility of this method, we expect these materials will be ideal candidates for applications in catalysis, adsorption, and separations. Furthermore, the implementation of this technology for production of three-dimensionally ordered macroporous materials can improve the cost and efficiency of metal oxide frameworks (MOFs) due to its high versatility and amenability to numerous systems.

摘要

通过胶体晶体模板和改进的溶胶-凝胶法的杂交,制备了三维有序分级多孔氧化铝、氧化铁、氧化钇和氧化镍。简单地说,高度有序的聚甲基丙烯酸甲酯(PMMA)阵列被金属盐和环氧化物的前体溶液渗透。材料的固化后的煅烧除去了聚合物模板,同时形成了反转副本。这些具有大孔窗口和介孔壁的分级结构通过粉末 X 射线衍射(PXRD)、热重分析(TGA)、扫描电子显微镜(SEM)和 N2 吸附/解吸技术进行了表征,以探测结构完整性。PXRD 表明,所制备的 3D 框架是具有 5 至 27nm 晶粒尺寸的单相多晶结构。TGA 研究的热稳定性说明了预期的 PMMA 模板的重量损失和完全分解。SEM 揭示了具有明确定义的大孔窗口和介孔壁的双模态、分级大孔框架。有序材料的气体吸附测量显示出高达 93m2g-1的比表面积和高达 33nm 的平均介孔直径。由于这种方法的多功能性,我们预计这些材料将成为催化、吸附和分离应用的理想候选材料。此外,由于其多功能性和对众多体系的适应性,该技术在三维有序大孔材料生产中的应用可以提高金属氧化物骨架(MOFs)的成本和效率。

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