Preparation method of double-textured ZnO:B films deposited by MOCVD on plasma etched polymer buffer was written by Addonizio, M. L.;Fusco, L.. And the article was included in Journal of Alloys and Compounds in 2015.Formula: C16H26O7 This article mentions the following:
With the aim of enhancing light trapping phenomenon in PV thin film silicon devices, a method was developed to produce highly textured TCO surfaces by the growth of ZnO:B on a buffer layer consisting of UV-cured highly transparent acrylic polymer (IBA) whose surface had been modified by RIE process. Different RIE etching conditions, particularly RF-power and process duration, were used to obtain different polymer surface modifications. The effect of different treatment conditions on polymer surface was systematically studied and subsequently correlated to the properties of ZnO:B films deposited by MOCVD on these modified polymer surfaces. The surface morphol. of zinc oxide film, growth on IBA buffer layer, changed from conventional pyramid-like single-texture to cauliflower-like double-texture. The morphol. of double-textured ZnO strongly depended on the surface properties of the etched polymer. Excellent scattering properties were obtained and at the wavelength of 800 nm the haze value increased from 7.5% (pyramidal-like single-texture ZnO layer on glass) to 68% (double textured ZnO film obtained on etched IBA, treated for 20 min at RF-power of 80 W). The root-mean-square roughness showed similar behavior: it increased at the increasing of the etching time and the highest value of 160 nm was obtained for cauliflower-like ZnO:B film. Good elec. properties were maintained for double-textured ZnO:B films with excellent scattering properties. In the experiment, the researchers used many compounds, for example, ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1Formula: C16H26O7).
((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Formula: C16H26O7
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts