Microfluidic System for Synthesis of Trigonal Selenium Nanowires
A microfluidic system was developed for the synthesis of trigonal selenium(t-Se) nanowires, which was composed of a glass microchip coupled with a poly(methyl methacrylate)(PMMA) microchip. In the glass microchip, amorphous selenium(a-Se) colloid was prepared by reducing selenious acid with an exces...
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description | A microfluidic system was developed for the synthesis of trigonal selenium(t-Se) nanowires, which was composed of a glass microchip coupled with a poly(methyl methacrylate)(PMMA) microchip. In the glass microchip, amorphous selenium(a-Se) colloid was prepared by reducing selenious acid with an excess amount of hydrazine at a temperature of 100 ℃. In the coupled PMMA microchip, a-Se was transformed into more stable t-Se seeds via sonication at room temperature. The residence time of the reactants in both microchips was optimized by varying the dimension and length of the microchannel each. The t-Se nanowires were formed by anisotropic growth of selenium crystallite during sonication and aging under the assistance of β-cyclodextrin(β-CD). Various stages of the nanowires' growth were investigated. The as-synthesized products were characterized by powder X-Ray diffraction(XRD), Raman spectroscopy, scanning electron microscopy(SEM), transmission electron microscopy(TEM) and selected-area electron diffraction(SAED). |
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In the glass microchip, amorphous selenium(a-Se) colloid was prepared by reducing selenious acid with an excess amount of hydrazine at a temperature of 100 ℃. In the coupled PMMA microchip, a-Se was transformed into more stable t-Se seeds via sonication at room temperature. The residence time of the reactants in both microchips was optimized by varying the dimension and length of the microchannel each. The t-Se nanowires were formed by anisotropic growth of selenium crystallite during sonication and aging under the assistance of β-cyclodextrin(β-CD). Various stages of the nanowires' growth were investigated. The as-synthesized products were characterized by powder X-Ray diffraction(XRD), Raman spectroscopy, scanning electron microscopy(SEM), transmission electron microscopy(TEM) and selected-area electron diffraction(SAED).</description><identifier>ISSN: 1005-9040</identifier><identifier>EISSN: 2210-3171</identifier><language>eng</language><publisher>College of Material Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 310036, P. R. China%College of Material Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 310036, P. R. China</publisher><subject>微流体系统 ; 扫描电子显微镜 ; 硒纳米线 ; 聚甲基丙烯酸甲酯 ; 聚(甲基丙烯酸甲酯) ; 透射电子显微镜</subject><ispartof>Chemical research in Chinese universities, 2010-07, Vol.26 (4), p.522-526</ispartof><rights>Copyright © Wanfang Data Co. Ltd. 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In the coupled PMMA microchip, a-Se was transformed into more stable t-Se seeds via sonication at room temperature. The residence time of the reactants in both microchips was optimized by varying the dimension and length of the microchannel each. The t-Se nanowires were formed by anisotropic growth of selenium crystallite during sonication and aging under the assistance of β-cyclodextrin(β-CD). Various stages of the nanowires' growth were investigated. The as-synthesized products were characterized by powder X-Ray diffraction(XRD), Raman spectroscopy, scanning electron microscopy(SEM), transmission electron microscopy(TEM) and selected-area electron diffraction(SAED).</description><subject>微流体系统</subject><subject>扫描电子显微镜</subject><subject>硒纳米线</subject><subject>聚甲基丙烯酸甲酯</subject><subject>聚(甲基丙烯酸甲酯)</subject><subject>透射电子显微镜</subject><issn>1005-9040</issn><issn>2210-3171</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNotj0tLxDAYRYMoWEf_Q3DnovDl0bTZKYMvGHUx47qkebSpnQSblpn59xbG1b2Lw-HeC5RRSiBnpCSXKCMARS6BwzW6SakHYFIInqHHD6_H6IbZG6_x9pQmu8cujksNU2eTTzg6vBt9G4Ma8NYONvh5jz9ViAc_2nSLrpwakr37zxX6fnnerd_yzdfr-_ppk2tKxJRLo4XVQLgtmCyhKgvBKkKgEZIYIIVRjSu4IsopAE4kAyEllU4Lp52hlq3Qw9l7UMGp0NZ9nMdlUqpbczx2x1NPYTnJAcTC3p9Z3cXQ_vqFbpT-cX6wNeOS0rJi7A_sU1Pk</recordid><startdate>20100725</startdate><enddate>20100725</enddate><creator>BIAN Tian-bin YIN Xue-feng LIU Jin-hua</creator><general>College of Material Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 310036, P. 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In the glass microchip, amorphous selenium(a-Se) colloid was prepared by reducing selenious acid with an excess amount of hydrazine at a temperature of 100 ℃. In the coupled PMMA microchip, a-Se was transformed into more stable t-Se seeds via sonication at room temperature. The residence time of the reactants in both microchips was optimized by varying the dimension and length of the microchannel each. The t-Se nanowires were formed by anisotropic growth of selenium crystallite during sonication and aging under the assistance of β-cyclodextrin(β-CD). Various stages of the nanowires' growth were investigated. The as-synthesized products were characterized by powder X-Ray diffraction(XRD), Raman spectroscopy, scanning electron microscopy(SEM), transmission electron microscopy(TEM) and selected-area electron diffraction(SAED).</abstract><pub>College of Material Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 310036, P. R. China%College of Material Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 310036, P. R. China</pub><tpages>5</tpages></addata></record> |
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subjects | 微流体系统 扫描电子显微镜 硒纳米线 聚甲基丙烯酸甲酯 聚(甲基丙烯酸甲酯) 透射电子显微镜 |
title | Microfluidic System for Synthesis of Trigonal Selenium Nanowires |
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