State Key Laboratory of Chemical Engineering, Membrane Science and Engineering R&D Lab, Chemical Engineering Research Center , East China University of Science and Technology , Shanghai 200237 , China.
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering , East China Normal University , Shanghai 200062 , China.
ACS Appl Mater Interfaces. 2018 May 2;10(17):15096-15103. doi: 10.1021/acsami.8b03561. Epub 2018 Apr 18.
A new microporous metal-organic framework (MOF) with formula {Co(oba)(3-bpdh)}4HO [oba = 4,4'-oxybis(benzoic acid); 3-bpdh = N, N'-bis-(1-pyridine-3-yl-ethylidene)-hydrazine] was assembled, and its morphology was found to undergo a microrod-to-nanosphere transformation with temperature variation. Core-shell Au@Pd functional nanoparticles (NPs) were successfully encapsulated in the center of the monodisperse nanospheres, and Pt NPs were well-dispersed and fully immobilized on the surface of Au@Pd@1Co to build the Pt/Au@Pd@1Co composites, which exhibited NPs catalytic activity for the reverse water gas shift reaction. The core-shell Au@Pd NPs in MOF significantly enchanced the CO selectivity of the catalyst, and the Pt NP loading on the surface of the nanosphere afforded a desirable CO conversion.
一种新的微孔金属-有机骨架(MOF),其化学式为{Co(oba)(3-bpdh)}4HO [oba = 4,4'-氧双(苯甲酸); 3-bpdh = N, N'-双-(1-吡啶-3-基-亚乙基)-肼],其形态随着温度的变化经历了从微棒到纳米球的转变。在单分散纳米球的中心成功封装了核壳 Au@Pd 功能纳米粒子(NPs),并且 Pt NPs 很好地分散并完全固定在 Au@Pd@1Co 的表面上,构建了 Pt/Au@Pd@1Co 复合材料,其表现出 NPs 对逆水气变换反应的催化活性。MOF 中的核壳 Au@Pd NPs 显著提高了催化剂的 CO 选择性,而纳米球表面上的 Pt NP 负载提供了理想的 CO 转化率。