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一种用于克级量产水溶性硫化锌纳米晶体粉末的简单胶体合成法。

A Simple Colloidal Synthesis for Gram-Quantity Production of Water-Soluble ZnS Nanocrystal Powders.

作者信息

Kho R, Torres-Martínez CL, Mehra RK

机构信息

Environmental Toxicology Graduate Program, Department of Neuroscience, University of California, Riverside, California, 92521

出版信息

J Colloid Interface Sci. 2000 Jul 15;227(2):561-566. doi: 10.1006/jcis.2000.6894.

Abstract

A simple, inexpensive, and reproducible procedure is described for large-scale synthesis of highly stable nanocrystalline ZnS powders. Cysteine-capped ZnS nanocrystals (NCs) were produced by a colloidal aqueous synthesis, employing a ligand-competition mechanism in which sulfide was introduced into a preformed zinc-cysteine solution. The synthesis procedure resulted in highly concentrated ZnS NC solutions ( approximately 100 mM) which could be ethanol-precipitated, redissolved, and dried to produce fine powders stable for more than 30 months at 4 degrees C. The NC powders were readily dissolved in aqueous solvents to concentrations as high as 300 mM. ZnS NCs could be prepared without cysteine capping, but only at extremely dilute concentrations ( approximately 0.2 mM ZnSO(4)) as per Sooklal et al. J. Phys. Chem. 100, 4551 (1996). The 30-month-old ZnS NC powders retained their original optical and photocatalytic properties and could be handled much like routine shelf chemicals, unaffected by ambient air or moderate moisture and temperature. UV/vis absorption spectroscopy showed band gap energies (E(g)) ranging from 4.82 eV (257 nm lambda(max)) to 4.47 eV (277 nm lambda(max)) for ZnS samples prepared with 0.25-2.0 initial sulfide ratios (as compared to zinc). Samples stored at 4 degrees C for 30 months showed equivalent band gap energies and spectral profiles. The average NC particle size was estimated to be 6.08+/-0.76 nm by high-resolution transmission electron microscopy. Selected-area electron diffraction and X-ray diffraction analyses concurred in suggesting a hexagonal crystal structure, with diffractions near d=3.1, 1.9, and 1.6 Å. The average NC composition of size-fractionated samples was estimated to be Cys(1)Zn(7)S(6). p-Nitrophenol, a model organic, was photocatalytically degraded using 30-month-old ZnS NC powders dissolved in an aqueous buffer. Rates of degradation (first-order rate constant k=0.261 min(-1); t(1/2)=2.66 min) were comparable to those of experiments using freshly prepared ZnS NCs (first-order rate constant k=0.247 min(-1); t(1/2)=2.80 min), further demonstrating the long-term stability of thus-produced NC powders. Copyright 2000 Academic Press.

摘要

本文描述了一种用于大规模合成高稳定性纳米晶ZnS粉末的简单、廉价且可重复的方法。通过胶体水相合成法制备了半胱氨酸封端的ZnS纳米晶体(NCs),采用配体竞争机制,将硫化物引入预先形成的锌-半胱氨酸溶液中。该合成方法得到了高浓度的ZnS NC溶液(约100 mM),可通过乙醇沉淀、重新溶解并干燥,以制备在4℃下稳定超过30个月的细粉。NC粉末很容易溶解在水性溶剂中,浓度高达300 mM。按照Sooklal等人在《物理化学杂志》100, 4551 (1996)中的方法,也可以在没有半胱氨酸封端的情况下制备ZnS NCs,但只能在极低的浓度(约0.2 mM ZnSO₄)下进行。30个月大的ZnS NC粉末保留了其原始的光学和光催化性能,并且可以像常规的货架化学品一样处理,不受环境空气或适度的湿度和温度影响。紫外/可见吸收光谱显示,对于初始硫化物与锌的比例为0.25 - 2.0制备的ZnS样品,其带隙能量(E(g))范围为4.82 eV(λmax = 257 nm)至4.47 eV(λmax = 277 nm)。在4℃下储存30个月的样品显示出等效的带隙能量和光谱轮廓。通过高分辨率透射电子显微镜估计平均NC粒径为6.08±0.76 nm。选区电子衍射和X射线衍射分析一致表明为六方晶体结构,在d = 3.1、1.9和1.6 Å附近有衍射。对按尺寸分级的样品的平均NC组成估计为Cys₁Zn₇S₆。使用溶解在水性缓冲液中的30个月大的ZnS NC粉末对模型有机物对硝基苯酚进行光催化降解。降解速率(一级速率常数k = 0.261 min⁻¹;t₁/₂ = 2.66 min)与使用新鲜制备的ZnS NCs的实验(一级速率常数k = 0.247 min⁻¹;t₁/₂ = 2.80 min)相当,进一步证明了由此制备的NC粉末的长期稳定性。版权所有2000年学术出版社。

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