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通过目标干扰金三角纳米棱柱状晶原位生长实现无标记、灵敏的比色法检测汞(II)

Label-free, sensitive colorimetric detection of mercury(II) by target-disturbed in situ seeding growth of gold triangular nanoprisms.

作者信息

Ling Rui, Zhang Qianqian, Ren Hang, Tursen Janar, Bi Junmin, Wu Zhenglong, Qin Weidong, Zhang Chenling

机构信息

College of Chemistry, Beijing Normal University, No. 19, XinJieKouWai Street, Beijing 100875, People's Republic of China.

出版信息

Nanotechnology. 2020 May 29;31(22):225501. doi: 10.1088/1361-6528/ab7584. Epub 2020 Feb 12.

Abstract

Gold nanomaterials have been used extensively in colorimetric detection of mercuric ions (Hg) due to their shape- and size-dependent, ultrastrong localized surface plasmon resonance (LSPR). Conventional detection was performed by first synthesizing the nanomaterials, and then applying them to signal-transducing reactions. We herein report a convenient method for detecting Hg based on gold triangular nanoprisms (AuTNPs). During the seeding-growth process, Hg added to the growth solution was co-reduced and deposited on the high-energy facets of the gold seeds, affecting the deposition patterns of the subsequently generated Au and ultimately leading to the formation of defective AuTNPs. Morphological changes were reflected by the in-plane dipole LSPR wavelength shift, which was proportionally related to the concentration of Hg. To improve the selectivity, the interference from Ag was eliminated by a stepwise preparation-selective precipitation approach. Under the optimized conditions, Hg could be selectively detected with 20 min, with a detection limit of 0.12 nM. Finally, the method was successfully applied to detecting trace Hg in fortified drinking, mineral and rain water samples, with recoveries ranging from 95.17% to 110.6%.

摘要

由于其形状和尺寸依赖性的超强局域表面等离子体共振(LSPR),金纳米材料已被广泛用于汞离子(Hg)的比色检测。传统检测方法是先合成纳米材料,然后将其应用于信号转导反应。我们在此报告一种基于金三角纳米棱镜(AuTNPs)检测汞的简便方法。在种子生长过程中,添加到生长溶液中的汞被共还原并沉积在金种子的高能面上,影响随后生成的金的沉积模式,并最终导致形成有缺陷的AuTNPs。形态变化通过面内偶极LSPR波长偏移反映出来,该偏移与汞的浓度成比例相关。为提高选择性,通过逐步制备-选择性沉淀方法消除了银的干扰。在优化条件下,20分钟内可选择性检测汞,检测限为0.12 nM。最后,该方法成功应用于检测强化饮用水、矿泉水和雨水样品中的痕量汞,回收率在95.17%至110.6%之间。

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