The phase transformation behavior of TiO 2 sol-gel synthesized nanopowder heated in a sealed quartz capillary from room temperature to 800°C was studied using in-situ synchrotron radiation diffraction (SRD). Sealing of the capillary resulted in an increase in capillary gas pressure with temperature. The pressures inside the sealed capillary were calculated using Gay-Lussac's Law, and they reached 0.36 MPa at 800°C. The as-synthesized material was entirely amorphous at room temperature, with crystalline anatase first appearing by 200°C (24 wt% absolute), then increasing rapidly in concentration to 89 wt% by 300°C and then increasing more slowly to 97 wt% by 800°C, with there being no indication of the anatase-to-rutile transformation up to 800°C. The best estimate of activation energy for the amorphous-to-anatase transformation from the SRD data was 10 (2) kJ/mol, which is much lower than that observed when heating the material under atmospheric pressure in a laboratory XRD experiment, 38(5) kJ/mol. For the experiment under atmospheric pressure, the anatase crystallization temperature was delayed by~200°C, first appearing after heating the sample to 400°C, after which crystalline rutile was first observed after heating to 600°C. The estimated activation energy for the anatase-to-rutile transformation was 120(18) kJ/mol, which agrees with estimates for titania nanofibers heated under atmospheric pressure. Thus, heating the nanopowders material under pressure promoted the amorphous-to-anatase transformation, but retarded the anatase-to-rutile transformation. This behavior is believed to occur in an oxygen-rich environment and interstitial titanium is also expected to form when the material is heated under high gas pressure. This suggests that atmospheric oxygen appears to accelerate the amorphousto-anatase transformation, whereas interstitial titanium inhibits TiO 2 structure relaxation, which is required for the anatase-to-rutile transformation.
K E Y W O R D STiO 2 nanopowders, anatase, rutile, sol-gel method, in-situ synchrotron radiation diffraction