Papers by Author: Chang Q. Sun

Abstract: In this paper, three types of titanium dioxide structures (anatase, heated amorphous and amorphous) from peroxo titanium complex were deposited on glass and wafer substrates by spraying technique. Influences of crystal structure, morphology and sodium ion on UV induced hydrophilicity were studied. X-ray diffraction revealed that crystalline anatase coatings are extremely hydrophilic (<10°) under UV irradiation (indoor) while the amorphous coatings are still hydrophobic on both glass and wafer substrate with contact angles as high as 70º. When amorphous coating was heated at 450°C, its structure was converted into crystalline anatase, and hence its UV induced hydrophilicity behavior on wafer substrate became similar to that of anatase. However, this UV induced hydrophilicity was inhibited on heated glass (450°C), suggesting that sodium ions in the glass might be responsible for the differences between silicon wafer and glass. With increasing coating thickness, such inhibition effect was reduced, but the hydrophilicity still could not reach the level of anatase. After 6 months of outdoor exposure, water contact angle for amorphous, heated amorphous and anatase were 61°, 26.6° and 12.1°, respectively. Also, X-ray diffraction suggested that amorphous is not converted into anatase after long period of UV exposure, although coating morphologies are changed based on Scanning Electron Microscopic observation. It is concluded that the crystal structure, coating morphology and sodium ion concentration have key impact on the photocatalytic properties on glass substrate.

Abstract: Shrinking the size of a solid down to nanometer scale is indeed fascinating, which makes all the otherwise constant physical quantities to be tunable such as the Young’s modulus, dielectric constant, melting point, etc. The variation of size also generates novel properties that can hardly be seen in the bulk such as the conductor-insulator and nonmagnetic-magnetic transition of noble metals at the nanoscale. Although the physics of materials at the nanoscale has been extensively investigated, the laws governing the energetic and dynamic behavior of electrons at such a scale and their consequences on the tunable physical properties of nanostructures have not been well understood [C. Q. Sun, Prog Solid State Chem 35, 1-159 (2007); Prog Mater Sci 54, 179-307 (2009)]. The objective of the contribution is to update the recent progress in dealing with the coordination-resolved energetic and dynamic behavior of bonds in the low-dimensional systems with consideration of the joint effect of temperature and pressure. It is shown that the broken-bond-induced local strain and the associated charge and energy quantum trapping at the defect sites perturbs the atomic cohesive energy, electroaffinity, the Hamiltonian and the associated properties of entities ranging from point defects, surfaces, nanocavities and nanostructures. Application of the theories to observations has led to consistent understanding of the behavior of nanometer-sized materials and the interdependence of these entities as well as the means of determining the bond energy through the temperature-dependent measurements.