Owen Rhodri E, Cortezon-Tamarit Fernando, Calatayud David G, Evans Enid A, Mitchell Samuel I J, Mao Boyang, Palomares Francisco J, Mitchels John, Plucinski Pawel, Mattia Davide, Jones Matthew D, Pascu Sofia I
Department of Chemistry University of Bath Claverton Down BA2 7AY UK.
Department of Electroceramics Instituto de Cerámica y Vidrio - CSIC Kelsen 5, Campus de Cantoblanco Madrid 28049 Spain.
ChemistryOpen. 2020 Feb 14;9(2):242-252. doi: 10.1002/open.201900368. eCollection 2020 Feb.
We report on the design and testing of new graphite and graphene oxide-based extended π-conjugated synthetic scaffolds for applications in sustainable chemistry transformations. Nanoparticle-functionalised carbonaceous catalysts for new Fischer Tropsch and Reverse GasWater Shift (RGWS) transformations were prepared: functional graphene oxides emerged from graphite powders via an adapted Hummer's method and subsequently impregnated with uniform-sized nanoparticles. Then the resulting nanomaterials were imaged by TEM, SEM, EDX, AFM and characterised by IR, XPS and Raman spectroscopies prior to incorporation of Pd(II) promoters and further microscopic and spectroscopic analysis. Newly synthesised 2D and 3D layered nanostructures incorporating carbon-supported iron oxide nanoparticulate pre-catalysts were tested, upon hydrogen reduction for the conversion of CO to CO as well as for the selective formation of CH and longer chain hydrocarbons. The reduction reaction was also carried out and the catalytic species isolated and fully characterised. The catalytic activity of a graphene oxide-supported iron oxide pre-catalyst converted CO into hydrocarbons at different temperatures (305, 335, 370 and 405 °C), and its activity compared well with that of the analogues supported on graphite oxide, the 3-dimensional material precursor to the graphene oxide. Investigation into the use of graphene oxide as a framework for catalysis showed that it has promising activity with respect to reverse gas water shift (RWGS) reaction of CO to CO, even at the low levels of catalyst used and under the rather mild conditions employed at atmospheric pressure. Whilst the γ-FeO decorated graphene oxide-based pre-catalyst displays fairly constant activity up to 405 °C, it was found by GC-MS analysis to be unstable with respect to decomposition at higher temperatures. The addition of palladium as a promoter increased the activity of the iron functionalised graphite oxide in the RWGS. The activity of graphene oxide supported catalysts was found to be enhanced with respect to that of iron-functionalised graphite oxide with, or without palladium as a promoter, and comparable to that of Fe@carbon nanotube-based systems tested under analogous conditions. These results display a significant step forward for the catalytic activity estimations for the iron functionalised and rapidly processable and scalable graphene oxide. The hereby investigated phenomena are of particular relevance for the understanding of the intimate surface morphologies and the potential role of non-covalent interactions in the iron oxide-graphene oxide networks, which could inform the design of nano-materials with performance in future sustainable catalysis applications.
我们报告了用于可持续化学转化应用的新型石墨和氧化石墨烯基扩展π共轭合成支架的设计与测试。制备了用于新型费托合成和逆水煤气变换(RGWS)转化的纳米颗粒功能化碳质催化剂:通过改良的Hummer法从石墨粉末中制备功能化氧化石墨烯,随后用尺寸均匀的纳米颗粒进行浸渍。然后,在引入Pd(II)促进剂并进行进一步的微观和光谱分析之前,通过透射电子显微镜(TEM)、扫描电子显微镜(SEM)、能量色散X射线光谱(EDX)、原子力显微镜(AFM)对所得纳米材料进行成像,并通过红外光谱(IR)、X射线光电子能谱(XPS)和拉曼光谱进行表征。测试了新合成的包含碳负载氧化铁纳米颗粒预催化剂的二维和三维层状纳米结构,在氢气还原后用于将CO转化为CO以及选择性生成CH和长链烃。还进行了还原反应,并对催化物种进行了分离和全面表征。氧化石墨烯负载的氧化铁预催化剂在不同温度(305、335、370和405°C)下将CO转化为烃,其活性与负载在氧化石墨上的类似物相当,氧化石墨是氧化石墨烯的三维材料前驱体。对氧化石墨烯作为催化框架的应用研究表明,即使在低催化剂用量和常压下相当温和的条件下,它对CO的逆水煤气变换(RWGS)反应也具有可观的活性。虽然γ-FeO修饰的氧化石墨烯基预催化剂在高达405°C时表现出相当恒定的活性,但通过气相色谱-质谱(GC-MS)分析发现,在较高温度下它对分解不稳定。添加钯作为促进剂提高了铁功能化氧化石墨在RWGS中的活性。发现氧化石墨烯负载催化剂的活性相对于有或没有钯作为促进剂的铁功能化氧化石墨有所增强,并且与在类似条件下测试的基于Fe@碳纳米管的体系相当。这些结果表明铁功能化且可快速加工和扩展的氧化石墨烯的催化活性评估向前迈出了重要一步。在此研究的现象对于理解氧化铁-氧化石墨烯网络中紧密的表面形态以及非共价相互作用的潜在作用具有特别重要的意义,这可为未来可持续催化应用中具有性能的纳米材料设计提供参考。