Trans. Nonferrous Met. Soc. China 22(2012) 117-123
Preparation of Cu nanoparticles with NaBH4 by aqueous reduction method
LIU Qing-ming1, 2, ZHOU De-bi1, 2, Yuya YAMAMOTO2, Ryoichi ICHINO2, Masazumi OKIDO2
1. School of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China;
2. Department of Materials Science, Graduate School of Engineering, Nagoya University, Nagoya 4648603, Japan
Received 12 January 2011; accepted 16 May 2011
Abstract: Cu nanoparticles were prepared by reducing Cu2+ ions with NaBH4 in alkaline solution. The effects of NaBH4 concentration and dripping rate on the formation of Cu nanoparticles were studied. The optimum conditions are found to be 0.2 mol/L Cu2+, solution with pH=12, temperature of 313 K and 1% gelatin as dispersant, to which 0.4 mol/L NaBH4 is added at a dripping rate of 50 mL/min. NH3·H2O is found to be the optimal complexant to form the Cu precursor. A series experiments were conducted to study the reaction process at different time points.
Key words: Cu nanoparticles; aqueous reduction method; precursor; reaction process
1 Introduction
In recent years, the preparation of Cu nanoparticles has become an intensive area of scientific research as Cu nanoparticles exhibit many excellent physical and chemical properties such as high electrical conductivity and chemical activity. Cu nanoparticles are considered possible replacements for Ag and Au particles in some potential applications, such as in catalysts and conductive pastes [1-4]. There are many well-known procedures for preparation of Cu nanoparticles, such as the radiation method [5], microemulsion technique [6], supercritical technique [7], thermal reduction [8], sonochemical reduction [9], laser ablation [10], metal vapor synthesis [11], vacuum vapor deposition [12] and aqueous reduction method [13]. Among these methods, aqueous reduction method is most widely employed because of its advantages such as simple operation, high yield and quality, limited equipment requirements and ease of control. Because of its strong reducing ability, NaBH4 is widely used as a reductant for this aqueous reduction process. According to the previously reported research, much work has been done to explore the optimum conditions for preparation of copper nanoparticles [14]. However, the reaction mechanism has been seldom reported. In this research, the mechanism of reaction process was investigated based on the optimizing of the reaction conditions.
2 Experimental
All the reagents used in the experiments were of analytical grade and obtained from Nacalai Tesque (Kyoto). The flowchart of the experimental process is shown in Fig. 1. Prior to carrying out the experiments, 50 mL CuSO4 solution and NaBH4 solutions were prepared, and argon was bubbled through both the solutions for 30 min. Each pH value was adjusted to the same value using H2SO4 and NaOH solutions, respectively. Then 1% gelatin (mass fraction) was added into the CuSO4 solution as a dispersant. The NaBH4 solution was then added dropwise to the CuSO4 solution in a beaker at 313 K with magnetic rod stirring. The color of the mixture was changed from blue to brown, indicating the precipitation of Cu nanoparticles. When the reaction was completed, a small quantity of the slurry was collected for size distribution measurements using an electrophoretic light scattering spectrophotometer (Model: ELS-8000NS, Otsuka Electronics Co. Ltd., Japan). Cu particles were formed by precipitation, which were separated by centrifugation, washed several times with distilled water and ethanol, and finally dried in a vacuum stove at room temperature for several days. The SEM images were obtained by using a scanning electron microscope (model: S-800, Hitachi Co. Ltd., Japan) and the XRD patterns of the specimen were recorded using an X-ray diffractometer (model: XRD-6000, Shimadzu Co. Ltd., Japan) with Cu Kα radiation.
Fig. 1 Flow chart of experiment process
3 Results and discussion
3.1 Effect of NaBH4 concentration on Cu nanoparticles preparation
In aqueous solution, the reaction takes place as
= (1)
In theory, the stoichiometric ratio of Cu2+ ions to NaBH4 is 4:1. In the experiment, Cu2+ concentration is fixed at 0.2 mol/L, thus, the NaBH4 concentration should ideally be 0.05 mol/L. With a fixed concentration (1%, mass fraction) gelatin as the dispersant and solution pH of 12, the effect of NaBH4 concentration on the Cu particles was investigated. The results are shown in Fig. 2. It is observed that the average size of the Cu nanoparticles decreases with increasing NaBH4 concentration. When the NaBH4 concentration is 0.4 mol/L (8 times greater than the stoichiometric dosage), Cu nanoparticles with an average size of 37 nm are obtained. The XRD patterns show that at a low NaBH4 concentration, the resultant particles contain Cu(OH)2 and Cu2O. At a higher NaBH4 concentration, the Cu(OH)2 contaminant disappears, but Cu2O disappears only when the NaBH4 concentration reaches several times the stoichiometric value. The analysis by XRD reveals that Cu(OH)2 and Cu2O contaminants are the intermediate products of the reduction process.
3.2 Effect of NaBH4 dripping rate on Cu nanoparticles preparation
In the experiments, it is found that the dripping rate has a significant effect on the average size and shape of the Cu nanoparticles. The effect of the NaBH4 dripping rate was investigated under constant condition of 0.2 mol/L Cu2+, 0.4 mol/L NaBH4, 1% gelatin and pH=12. The Cu particles were prepared with the NaBH4 dripping rate of 5 and 50 mL/min, respectively. The results of this experiment are shown in Fig. 3. The average size of Cu particles prepared at a dripping rate of 5 mL/min is larger than that obtained at 50 mL/min. Traces of Cu(OH)2 are also found, indicating that the reduction reaction is incomplete. The Cu nanoparticles obtained at dripping rate of 50 mL/min are smaller due to the occurrence of explosive nucleation when the two solutions are combined. According to the classical theory of nucleation, formation of Cu nanoparticles usually undergoes three stages: pre-nucleation, nucleation and crystal nucleus growth [15]. Explosive nucleation involves the generation of a large number of nuclei during the initial stages of nucleation. Since most of the Cu2+ ions are consumed for nucleation, the aggregation is limited. Thus, Cu nanoparticles with very small size can be obtained.
3.3 Effect of complexant on Cu nanoparticles preparation
Appropriate complexants in the CuSO4 solution could not only eliminate the agglomeration of the Cu particles, but also change the morphology of the resultant particles. In this work, three types of complexants were adopted in the experiments, NH3·H2O, potassium sodium tartrate (KNaC4H4O6) and trisodium citrate (C6H5O7Na3). The reduction reactions can be represented by the following equations.
When NH3·H2O is adopted as complexant,
= (2)
=
(3)
Fig. 2 SEM images and XRD patterns of copper particles obtained using NaBH4 with different concentration: (a), (a′) 0.05 mol/L; (b), (b′) 0.1 mol/L; (c), (c′) 0.2 mol/L; (d), (d′) 0.4 mol/L
When KNaC4H4O6 is adopted as complexant,
= (4)
=
(5)
And when C6H5O7Na3 is adopted as complexant,
= (6)
=
(7)
With fixed values of 0.2 mol/L Cu2+, 0.4 mol/L NaBH4, 1% gelatin and pH of 12, the effect of different complexants on Cu nanoparticles preparation was investigated. The results are shown in Fig. 4. With 1.2 mol/L NH3·H2O, 0.6 mol/L KNaC4H4O6 and 0.6 mol/L C6H5O7Na3 as the complexants, the average sizes of Cu particles obtained are 42, 115 and 108 nm, respectively. Thus, NH3·H2O is the optimal complexant for precursor formation.
Fig. 3 SEM images and XRD patterns of copper particles obtained using NaBH4 at different dripping rates: (a), (a′) 5 mL/min; (b), (b′) 50 mL/min
Fig. 4 SEM images of copper particles obtained using different complexants: (a) 1.2 mol/L NH3·H2O; (b) 0.6 mol/L KNaC4H4O6; (c) 0.6 mol/L C6H5O7Na3
3.4 Reduction process at different reaction time
A series experiments were conducted to study the reactions occurring during Cu nanoparticles formation. At fixed values of 0.2 mol/L Cu2+, 0.4 mol/L NaBH4, 1% gelatin and pH=12, the size distribution, SEM images and XRD patterns of the Cu nanoparticles at different reaction time points (0, 0.5, 1, 3, 5, 10 and 60 min) were examined. The results are shown in Fig. 5. The SEM images and XRD patterns show that during the initial stages of the reaction, the majority of the particles is rod-shaped Cu(OH)2. Within 5 min, Cu(OH)2 disappeared. The XRD patterns at 10 and 60 min are similar to that obtained at 5 min, indicating the completion of the reduction reaction within 5 min. The XRD patterns also show that all the Cu2+ ions are transformed to Cu(OH)2 before the two solutions are mixed. Cu(OH)2 is then reduced to Cu nanoparticles by NaBH4. The final reaction process can be represented as
= (8)
= (9)
Fig. 5 SEM images and XRD patterns of copper particles obtained at different time points: (a), (a′) Before mixing; (b), (b′) After 0.5 min; (c), (c′) After 1 min; (d), (d′) After 3 min; (e), (e′) After 5 min; (f), (f′) After 10 min; (g), (g′) After 60 min
4 Conclusions
1) The average size of the Cu nanoparticles reduces with increasing excess of NaBH4 to Cu2+. When the Cu2+ and NaBH4 concentration are 0.2 and 0.4 mol/L, the dripping rate is 50 mL/min, gelatin concentration is 1%, pH=12 and solution temperature is 313 K, the finest Cu nanoparticles (37 nm) are obtained.
2) Among NH3·H2O, KNaC4H4O6 and C6H5O7Na3, the optimal complexant is found to be NH3·H2O for precursor formation. The smallest Cu nanoparticles are obtained with 1.2 mol/L NH3·H2O.
3) During the reaction process, Cu2+ is transformed to Cu(OH)2 before combination of the solutions and then this Cu(OH)2 is reduced by the addition of NaBH4 solution.
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NaBH4的水性还原法制备纳米铜颗粒
刘清明1, 2,周德璧1, 2,山本雄也2,市野良一2,兴户正纯2
1. 中南大学 化学化工学院,长沙 410083,中国;
2. 名古屋大学 工学研究科 材料科学专业,名古屋 4648603,日本
摘 要:在碱性溶液中用NaBH4还原Cu2+制备纳米铜颗粒,研究NaBH4浓度和滴加速率对Cu纳米颗粒制备的影响。反应的最佳条件是:0.2 mol/L Cu2+,溶液pH 12,温度313 K,1%明胶作为分散剂,将0.4 mol/L NaBH4溶液以50 mL /min的速率加入CuSO4溶液中。氨水是最佳的络合剂。采用一系列实验研究不同时间点的反应进程。
关键词:纳米铜颗粒;水性还原法;前驱体;反应进程
(Edited by FANG Jing-hua)
Corresponding author: LIU Qing-ming; Tel: +81-52-789-3353; Fax: +81-52-789-3355; E-mail: luisman@126.com
DOI: 10.1016/S1003-6326(11)61149-7