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The silicification of DNA origami structures increases their mechanical and thermal stability and provides chemical protection. So far, it is unclear how silicification affects the internal structure of the DNA origami and whether the whole DNA framework is embedded or if silica just forms an outer shell. By using in situ small-angle X-ray scattering (SAXS), we show that the net-cationic silica precursor TMAPS induces substantial condensation of the DNA origami, which is further enhanced by the addition of TEOS at early reaction times to an almost 10 % size reduction. We identify the SAXS Porod invariant as a reliable, model-free parameter for the evaluation of the amount of silica formation at a given time. Contrast matching of the DNA double helix Lorentzian peak reveals that silica growth also occurs on the inner surfaces of the origami. The less polar silica forming within the origami structure, replacing more than 40 % of the internal hydration water causes a hydrophobic effect: origami condensation. In the maximally condensed state, thermal stabilization of the origami up to 60 {\deg}C could be observed. If the reaction is driven beyond this point, the overall size of the silicified origami increases again due to more and more silica deposition on the DNA origami. DNA origami objects with flat surfaces show a strong tendency towards aggregation during silicification, presumably driven by the very same entropic forces causing condensation. Our studies provide novel insights into the silicification reaction and hints for the formulation of optimized reaction protocols.

Photoresponsive materials feature properties that can be adjusted near- instantaneously, reversibly, and with high spatiotemporal precision, by light. There is considerable interest in maximising the degree of switching, and in measuring this degree during illumination in complex environments. We study the switching of photoresponsive lipid membranes that allow precise and reversible manipulation of membrane shape, permeability, and fluidity. Though these macroscopic photoresponses are clear, it is unclear how large the changes of trans/cis ratio are, and whether they can be improved. Here, we used small-angle X-ray scattering to measure the thickness of photoswitchable lipid membranes, and correlate thickness to trans/cis ratios. This revealed an unexpected dependency of photoswitching upon aqueous phase composition, highlighting smaller-than-expected photoswitching with deionized water, and showed thickness variations twice as large as previously observed. Soft X-rays can quantitatively isomerise photolipid membranes to the all- trans state: both enabling more powerful X-ray-based membrane control and underlining the role of high energy X-rays for observation-only soft matter experiments.