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Highly Sensitive and Selective Colorimetric Sensing of Hg2+ Based on the Morphology Transition of Silver Nanoprisms

机译:基于银纳米棱镜形态学转变的Hg2 +的高灵敏度和选择性比色传感

摘要

A simple colorimetric approach for mercury ion (Hg2+) sensing was developed that was based on the Hg2+. induced deprotection and morphology transition of 1-dodecanethiol (C12H25SH)-capped silver nanoprisms (Ag NPRs) upon the presence of iodides at room temperature. The abstraction of C12H25SH from the surface of Ag NPRs by Hg2+ led to their deprotection of Ag NPRs and the formation of complexation between silver ions and excess iodide ions. Also, the silver atoms were consumed and moved from the surface of Ag NPRs, accompanying the changes in the particle morphology that resulted in a change of color and UV-vis absorption spectra of the colloidal solution. With increasing concentrations of Hg2+ from 10 to 500 nM, the surface plasma resonance spectral band of Ag NPRs emerged as a blue shift and exhibited a good linear relationship, and the limit of detection was 3.3 nM. Furthermore, the developed method was applied for detecting Hg2+ in different real water samples with satisfying recoveries over 92%.
机译:开发了一种基于Hg2 +的汞离子(Hg2 +)感测的简单比色方法。在室温下存在碘化物时,可诱导1-十二烷硫醇(C12H25SH)封端的银纳米棱镜(Ag NPR)的脱保护和形态学转变。 Hg2 +从Ag NPRs表面提取C12H25SH导致它们对Ag NPRs脱保护,并在银离子和过量碘离子之间形成络合物。同样,银原子被消耗并从Ag NPR的表面移走,伴随着颗粒形态的变化,这导致了胶体溶液的颜色和UV-vis吸收光谱的变化。随着Hg2 +浓度从10 nM增加到500 nM,Ag NPRs的表面等离子体共振谱带出现蓝移并表现出良好的线性关系,检出限为3.3 nM。此外,该方法用于实际水样中Hg2 +的检测,回收率达92%以上。

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