Temperature profoundly influences nanoscale organization in polymers, soft matter, colloids, and functional materials. Heating, cooling, or thermal cycling can trigger phase transitions, modify domain spacing, alter crystalline order, or initiate structural rearrangements that directly affect mechanical, optical, and electronic properties.
Small-Angle and Wide-Angle X-ray Scattering (SAXS/WAXS) provide a direct, non-destructive way to follow these transformations in situ. Because SAXS and WAXS probe complementary length scales, they reveal how thermal conditions reshape materials from the atomic lattice to the mesostructure.
Temperature-controlled SAXS/WAXS experiments capture how structure evolves as thermal energy drives reorganization. From scattering data, one can extract:
Figure 1. Thermal hysteresis in an organic photovoltaic donor material
SAXS/WAXS measurements on a dithienocyclopenta-thieno[3,2-b]thiophene (DTCTT)–based small-molecule donor reveal clear hysteresis during heating–cooling cycles. Changes in scattering patterns highlight the interplay between molecular packing and mesoscale ordering as temperature varies. See Y. Abe et al., Unique Reversible Crystal-to-Crystal Phase Transition—Structural and Functional Properties of Fused Ladder Thienoarenes, Chem. Mater. 29.18, (2017). DOI: 10.1021/acs.chemmater.7b0122
These measurements allow researchers to map complete thermal trajectories and understand how nanoscale structure governs macroscopic performance.
Temperature-induced structural evolution can be studied in an exceptionally wide range of materials, including:
Both heating and cooling modes allow detailed mapping of reversible and irreversible phenomena.
Temperature-controlled SAXS/WAXS provides a unique window into how materials reorganize across multiple length scales when heated or cooled.
Allowing detection of nanoscale rearrangements, domain changes, and phase transitions as they occur.
Combining SAXS sensitivity to mesoscale periodicities with WAXS access to crystalline order for a unified picture of thermal response.
Enabling precise tracking of spacing, crystallinity, correlation lengths, and ordering throughout heating or cooling cycles.
Capturing reversible and irreversible transformations without removing, altering, or interrupting the sample.
Supporting cryogenic, ambient, and high-temperature conditions while maintaining stable measurement geometry and data quality