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Solar‐Light‐Driven CO<sub>2</sub> Reduction by CH<sub>4</sub> on Silica‐Cluster‐Modified Ni Nanocrystals with a High Solar‐to‐Fuel Efficiency and Excellent Durability
154
Citations
44
References
2018
Year
EngineeringEnergy ConversionColloidal NanocrystalsNatural Gas ResourcesNanocatalysisChemistryHydrogen GenerationChemical EngineeringNanoscale ChemistryNanostructure SynthesisRenewable Solar EnergyEnergy ApplicationsMaterials ScienceCatalytic ApplicationNanotechnologyCatalysisCatalytic ProcessNanocrystalline MaterialGlobal Co 2NanomaterialsHigh Solar‐to‐fuel EfficiencyCatalyst PreparationSilica‐cluster‐modified Ni NanocrystalsExcellent DurabilitySolar Cell Materials
Abstract Catalytic CO 2 reforming of CH 4 (CRM) to produce syngas (H 2 and CO) provides a promising approach to reducing global CO 2 emissions and the extensive utilization of natural gas resources. However, the rapid deactivation of the reported catalysts due to severe carbon deposition at high reaction temperatures and the large energy consumption of the process hinder its industrial application. Here, a method for almost completely preventing carbon deposition is reported by modifying the surface of Ni nanocrystals with silica clusters. The obtained catalyst exhibits excellent durability for CRM with almost no carbon deposition and deactivation after reaction for 700 h. Very importantly, it is found that CRM on the catalyst can be driven by focused solar light, thus providing a promising new approach to the conversion of renewable solar energy to fuel due to the highly endothermic characteristics of CRM. The reaction yields high production rates of H 2 and CO (17.1 and 19.9 mmol min −1 g −1 , respectively) with a very high solar‐to‐fuel efficiency (η, 12.5%). Even under focused IR irradiation with a wavelength above 830 nm, the η of the catalyst remains as high as 3.1%. The highly efficient catalytic activity arises from the efficient solar‐light‐driven thermocatalytic CRM enhanced by a novel photoactivation effect.
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