Nickel oxide reduction studied by environmental TEM and in situ XRD

Publication: Research - peer-reviewConference abstract in proceedings – Annual report year: 2012

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Nickel oxide reduction and subsequent Ni behaviour under H2 is of practical importance in the field of solid oxide fuel cell (SOFC) technology, as it determines the structure of the electronic conductor on the anode side during operation [1]. Despite extensive coverage in the literature [2], several questions remain, notably regarding the NiO reduction kinetics and its structural evolution.
Here, we perform in situ reduction of an industrial NiO powder from JT Baker™ under 1.3 mbar of H2 (2 mlN/min) in a differentially pumped FEI Titan environmental transmission electron microscope (ETEM) [3]. Images, diffraction patterns and electron energy-loss spectra are acquired during different temperature ramps (300 to 600°C) in order to monitor the structural and chemical evolution of the system. Similar experiments are performed in a PANalytical X'Pert PRO X-ray diffractometer equipped with an Anton Paar furnace and a mass spectrometer to complement and extrapolate the ETEM data to higher pressures and gas flows. Diffraction peak intensities, crystallite sizes (obtained using the Scherrer formula) and H2/H2O mass spectrometer signals are monitored.
The recorded images and diffraction patterns show that the nucleation of Ni on NiO takes place at temperatures below 400°C and is either epitaxial with a small angle misfit in thin specimen areas (Fig. 1) or randomly oriented in thicker regions. Reduction proceeds through the growth of Ni domains and the movement of interfaces, the latter inducing particle shrinkage and pore creation within larger particles. Densification is observed when the temperature approaches 600°C: the porosity that was created at lower temperatures disappears. This reorganization of Ni is detrimental to the connectivity of the Ni catalyst and to the reduction-reoxidation stability of the SOFC [4].
Reaction kinetics are measured in the ETEM by electron energy-loss spectroscopy using two different techniques based on changes of the Ni L2,3 white lines upon reduction (either taking the ratio of the Ni L3 and L2 integrated intensities or using multiple linear least squares fitting of NiO and Ni experimental reference spectra [5,6]). Reduction starts earlier but at a higher temperature when the heating rate is increased (380°C at 2°C/min compared to 420°C at 7°C/min). The initiation of the reduction depends on the number of oxygen surface vacancies, which in turn depends on the temperature and time [7]. Reduction proceeds quickly until the remaining NiO fraction reaches a level of about 30% (Fig. 2). The reaction then slows down and full reduction is only achieved at temperatures above 600°C (confirmed using diffraction). This decrease in reaction rate appears to be caused by physical factors, as NiO reduction is known to be autocatalytic [2]. As only a few micrograms of reducible material are dispersed on the TEM grid and considering the volume of the reaction chamber in the ETEM (~800 cm3), a shortage of reactive gas is unlikely even in 2 mbar of H2. It is probable that the presence and stagnation of H2O vapour created upon reduction blocks H2 access to the reactive sites, decreasing the reaction rate at a high conversion fraction. The gas flow is low and may not evacuate the product gas efficiently around the Ni(O) particles. Complementary XRD experiments point towards the same conclusion and underline the impact of the pressure and gas flow on the kinetics.
It is possible to determine an approximate activation energy for NiO reduction inside the ETEM using the Kissinger method [8], which is based on measurements of the shift in the temperature at which the reaction rate is maximum for different heating rates. With EELS experiments performed at 2, 4 and 7 °C/min, an activation energy of ~70 ± 20 kJ/mol is obtained, which is consistent with values found in the literature [2].
Original languageEnglish
Title of host publicationEMC2012 proceedings
Number of pages2
Publication date2012
StatePublished

Conference

Conference15th European Microscopy Congress 2012
CountryUnited Kingdom
CityManchester
Period16/09/1221/09/12
Internet addresshttp://www.emc2012.org.uk/

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Oral presentation.

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