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Preparation of Porous In 2 O 3 Powders by Ultrasonic-spray Pyrolysis Employing PMMA Microspheres Synthesized by Emulsion Polymerization and Their Gas-sensing Properties
| Content Provider | Semantic Scholar |
|---|---|
| Author | Hyodo, Takeo Furuno, Shu-Ichi Fujii, Eriko Katsuhide, Matsuo Motokucho, Suguru Kojio, Ken Shimizu, Yasuhiro |
| Copyright Year | 2012 |
| Abstract | The suspension containing polymethylmethacrylate (PMMA) microspheres was synthesized by the emulsion polymerization employing methyl methacrylate monomer, sodium lauryl sulfate as a surfactant and ammonium persulfate as an initiator, and porous In2O3powders(pr-In2O3(M), M: In2O3 source (N: In(NO3)3, Cl: InCl3))were prepared by ultrasonic-spray pyrolysis of In(NO3)3 or InCl3 aqueous solution containing the synthesized PMMA microspheres as a template. The average diameter of the PMMA microspheres, which was measured by dynamic light scattering, was ca. 60.2 nm. The pr-In2O3(N) powder consisted of large microspheres with well-developed spherical mesopores (≤ ca. 30 nm in diameter) and a small number of macropores (ca. 100 nm in diameter) on the spherical surface, while the pr-In2O3(Cl) powder was composed of meso-sized particles (ca. 30 nm in diameter), respectively. On the other hand, the morphology of conventional In2O3 powder (c-In2O3(N)) prepared by ultrasonic-spray pyrolysis of PMMA-free In(NO3)3 aqueous solution as a reference was roughlyspherical with a diameter of ca. 100~700nm and the bulk was relatively dense. The NO2 response of pr-In2O3(M) sensors was much larger than that of a c-In2O3(N) sensor. In addition, the response and recovery speeds of the pr-In2O3(M) sensors were faster than those of the c-In2O3(N) sensor. |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | https://www.ama-science.org/proceedings/download/ZGN0ZN== |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |