期刊論文
學年 | 98 |
---|---|
學期 | 2 |
出版(發表)日期 | 2010-02-01 |
作品名稱 | INFLUENCE OF CONSTITUTION OF HYBRID FERROCENYL ALKANETHIOLS SELF-ASSEMBLED MONOLAYERS TO INTERFACIAL CHARACTERISTICS ON GOLD SURFACE |
作品名稱(其他語言) | |
著者 | Chu, Shu-fang; Lin, Yun-han; Huang, Jhen-gang; Lin, Chii-wann |
單位 | 淡江大學化學學系 |
出版者 | Singapore: World Scientific Publishing Co. Pte. Ltd. |
著錄名稱、卷期、頁數 | Biomedical Engineering: Applications, Basis and Communications 22(1), pp.25-31 |
摘要 | The interfacial characteristics of self-assembled monolayer (SAM), that are applied in miniaturized sensor design, were strongly influenced by the SAM constitution. The electrochemical and interfacial characteristics of hybrid SAMs that constituted with ferrocenyl octanethiol (FcC8SH) and unsubstituted octanethiol (C8) or 2-mercaptopyrimidine (2-MPD) were investigated in this study. The peaks of anodic oxidation were observed at around 0.49 V (vs. Ag/AgCl) in the FcC8SH/C8 hybrid SAM. However, the oxidation potentials descended from 0.42–0.38 V as the molar fraction of FcC8SH was decreased from 0.8–0.2 in the FcC8SH/2-MPD hybrid SAM. On the other hand, the interfacial hydrophilicity of FcC8SH/2-MPD hybrid SAM was measured to be higher than the FcC8SH/C8 hybrid SAM due to the random arrangement of SAM caused by the shape of 2-MPD. Then, the surface roughness of hybrid SAM and chain length of ferrocenyl alkanethiols were all considered to be the parameters of interfacial characteristics. In summary, doping of 2-MPD in SAMs might reduce the rigidity of ferrocenyl alkanethiol SAMs and increase the interfacial hydrophilicity. This result will be useful in the development of the low power consumption portable bioanalytical system. And a miniaturized bioanalytical system based on ferrocenyl SAMs would be developed in the future. |
關鍵字 | Hybrid self-assembled monolayer; Ferrocenyl alkanethiol; Interfacial hydrophilicity |
語言 | en |
ISSN | 1016-2372; 1793-7132 |
期刊性質 | 國外 |
收錄於 | SCI EI |
產學合作 | |
通訊作者 | Lin, Chii-wann |
審稿制度 | 否 |
國別 | SGP |
公開徵稿 | |
出版型式 | ,電子版,紙本 |
相關連結 |
機構典藏連結 ( http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/58247 ) |