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In this work, we describe the sensing behavior of silver nanoprisms and nanosphere of comparable size or comparable shape, at room temperature by using UV-visible spectroscopy. The sensing mechanisms were analyzed by transmission electron microscopy and electrochemistry. These two nanomaterials showed to be fast and efficient sensors for Hg2+ without adding any masking agent. The sensor extinction response at 428 nm was in linear relationship for Hg2+ between 10 ppb to 3 ppm by silver nanospheres with a theoretical detection limit of 3 ppb. The calibration curve of the silver nanoprisms showed the extinction ratio value at 758 nm divided by 490 nm decreased linearly over the Hg2+ concentration range of 20 ppb to 1 ppm with a theoretical detection limit of 10 ppb. The silver nanoprisms showed greater blue shift than nanospheres and the better selectivity for Hg2+. Then silver nanoprisms and nanospheres of comparable absorbance had been investigated to learn the shape dependant behavior respectively, which showed better sensing capacity at higher wavelength for both of them. The electrochemistry of silver nanospheres and nanoprisms had been investigated to ascertain the silver nanomaterial surface change before and after sensing. It showed the original silver nanoprisms showed greater oxidation activity than nanospheres, by which we assumed the greater activity might be responsible for the better sensing selectivity. After sensing, the oxidation peak for both silver nanospheres and nanoprisms changed to more positive potential because of the formation of amalgam. It was possible to use this approach in applications for the analysis of Hg2+ in contaminated waters especially by nanoprisms.

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phu_grassman

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greatsupercat(½ð±Ò+10, ·­ÒëEPI+1): Ð޸ĵķdz£ºÃ£¬Èùý¾õµÃÁì½ð±ÒʹÓøüÓÐÒâÒåÁË£¬·Ç³£¸Ðл¡£ 2011-08-19 16:01:41

In our work, we describled the sensing behavior of silver nanoprisms and nanospheres of comparable size or shape at room temperature by using UV-vis spectroscopy. The sensing mechenisms were analyzed by transmission electron micropscopy and electrochemistry. The study on the two kinds of nanomaterial indicated that they can be used as fast and efficient sensors for Hg2+ without adding any masking agents. There was a linear relationship with Hg2+ within the range of 10 ppb to 3 ppm for the quenching reaction at 428nm, with a theoretical detection limit of 3 ppb. The calibration curve of the silver nanoprisms showed a linear relationship held for the value of the absorption at 490nm devided by that at 758nm between 10ppb and 1ppm, with a theoretical detection limit of 20 ppb. The silver nanoprisms showed greater blue shift than the silver nanospheres and  better selectivity for Hg2+. Then we investigated the bahavior of the silver nanoprism sensor and the nanosphere sensor respectively and found that they showed better sensing capacity at higher wavelengths. The electrochemical analysis of silver nanospheres and nanoprisms was carried to ascertain the change of the silver materials before and after reacting with Hg.  It showed the original silver nanospheres showed greater oxidation ability than the nanoprisms, of which we assumed the greater ability might be responsible for the better selectivity. After sensing, the oxidation peak for both the silver nanospheres and the nanoprisms moved to a more positive potential because of the formation of amalgam. Finally, the silver nanoprisms proved to be the more promising sensor for the  analysis of Hg2+ in contaminated waters.


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