The formation of cermet materials via the addition of electrolyte ceramic to metal-based electrodes has become widely adopted in solid oxide fuel cell fabrication due to its benefits in maximizing triple-phase boundary densities, while mitigating bulk thermal expansion mismatch between electrode and electrolyte layers. This work improves thermo-mechanical understanding via examination of nickel-based anode materials using synchrotron X-ray diffraction; two cermet materials are studied: Ni-YSZ and Ni-GDC, with comparison to a ceramic-free Ni sample. Findings conclude that although the ceramic addition has minor effects on the cubic Ni structure within isothermal environments, stress induced by the different thermal properties within the cermet materials results in a shifted Ni thermal expansion peak on passing the Curie point. Moreover, extended cycling of the Ni-YSZ sample suggests that low-temperature operation (ca. 600 ℃) may require several thermal cycles, or extended dwell times, to alleviate residual Ni stresses, this has potential implications for SOFC design and operation strategies. Highlights The effects of ceramic addition to the expansion of the cubic structure of Ni in isothermal environments are minor over a single thermal cycle. Accelerated stress tests revealed that lower temperature operation, i.e. 600 ℃ rather than higher 1000 ℃, results in deformation of the lattice parameters at both, low and high temperatures, likely due to a combination of two mechanisms: shock-induced tensile stress and delayed relaxation hysteresis. High and low temperature deformation has been found to be divergent resulting in a greater relative deformation in the cold lattice parameters. The thermal expansion non-linearity on passing the Ni Curie temperature is not suppressed; however, it is shifted to a higher temperature, a temperature that is dependent upon the ceramic employed.