The surface modification by Al2O3 deposition is considered to be mostly responsible for the reduction of water contact angle, although the cracks on the deposited Al2O3 film also contributes to the reduction

of water contact angle, which is confirmed by the FTIR measurements, as shown in Figure 6. The changes in the FTIR spectra are clearly found at the bands of 793, 848, 1,020, 1,123 to 1,104, 1,245, 1,340, 3,429, and 2,968 cm−1, [20–23]. Among them, the absorption peak at 3,429 cm−1, corresponding to the hydroxyl group (−OH) [20, 23], plays an important role in the film growth in ALD and the reduction Compound Library supplier of water contact angle. Figure 6 FTIR spectra. (a) Uncoated PET, the Al2O3-coated PET films by (b) ALD, (c) ALD with plasma pretreatment, and (d) PA-ALD. Inhibitor Library in vivo The amplitude of the absorption peak at 3,429 cm−1 is found to be enhanced with the Al2O3 deposition by ALD, especially with the introduction of plasmas in ALD, which suggests the MK 8931 in vitro elevated density of -OH group on the surface of Al2O3 film deposited by PA-ALD. The -OH groups, acting as the reactive nucleation sites, are important to improve the quality of the deposited films in terms of uniformity and conformal film coverage without substantial subsurface growth [24]. Chemical composition of the deposited Al2O3 film Surface modification in terms of wettability obtained by ALD with and without plasma assistance

is dependent on the chemical composition of the deposited Al2O3 films, which is revealed by the XPS spectra of the uncoated and coated PET film, as shown in Figure 7. It shows the peaks at the binding energies of 284 and 531 eV, corresponding to the C 1s and the O 1s, respectively, with the uncoated PET film, as shown in Figure 7a. With the deposition of Al2O3 film by PA-ALD, another peak at the binding energy of 74 eV, corresponding to the Al 2p, is found in Figure

7b, and the L-gulonolactone oxidase relative content of O 1s is elevated, both of which are confirmed by the relative element contents shown in Figure 7c. The increment of O 1s content and the emergence of Al 2p are achieved for the Al2O3 film deposited by ALD, plasma pretreated ALD, and PA-ALD. Further investigation on the chemical structure of the uncoated and the coated PET surface are carried out by the high-resolution XPS analysis of C 1s, O 1s, and Al 2p. The concentration of each chemical component of C1s and O1s is examined by using Gaussian fit and shown in Figures 8 and 9. Figure 7 XPS spectra. (a) Uncoated PET, (b) the Al2O3-coated PET film by PA-ALD, and (c) relative elemental contents. Figure 8 XPS spectra of C 1 s peaks. With (a) uncoated PET, (b) the Al2O3-coated PET film by PA-ALD, and (c) relative elemental contents. Figure 9 XPS spectra of O 1 s peaks. With (a) uncoated PET, (b) the Al2O3-coated PET film by PA-ALD, and (c) relative elemental contents.