- Nano Express
- Open Access
The phase transformation of CuInS2 from chalcopyrite to wurtzite
© Xie et al.; 2015
- Received: 20 December 2014
- Accepted: 4 February 2015
- Published: 27 February 2015
In the present work, CuInS2 nanoparticles have been successfully synthesized by water-bath method with deionized water as solvent and thioglycolic acid as complexing agent at 80°C. The phase transition of CuInS2 from chalcopyrite to wurtzite was realized by adjusting the pH value of reaction solution. The emergence of Cu2S in the condition of higher pH value of reaction solution led to the formation of wurtzite CuInS2. This facile method that controls the phase structure by adjusting the solution pH value could open a new way to synthesize other I-III-VI2 ternary semiconductor compounds.
With increasing global energy consumption, the fabrication of pollution-free, low-cost, and high-efficiency photovoltaic cells has attracted successive attention in recent years. As an I-III-VI2 ternary semiconductor compound with a direct bandgap of 1.5 eV at room temperature, CuInS2 is a promising material for photovoltaic applications because of its low toxicity, high absorption coefficient, and high theoretical photovoltaic conversion efficiency (about 25% to 30%) [1-3].
In the previous studies, CuInS2 has been found to exist in three different crystal structures: chalcopyrite, zinc blende, and wurtzite [4-6]. Chalcopyrite CuInS2 is the most common existing phase at room temperature, whereas those with zinc blende and wurtzite structures are stable only at high temperatures. Different from those of chalcopyrite phase CuInS2, the indium and copper atoms of wurtzite CuInS2 are randomly distributed over the cation sites of the lattice which allows the flexibility of stoichiometry and easily tuning the Fermi energy over a wider range [1,7,8]. Due to the differences in structure, wurtzite CuInS2 not only exhibits different optical properties but also may present novel properties which can expand its application. Therefore, it is meaningful to develop an effective route to realize the controlled synthesis of CuInS2 with different phase structures. Most of the reports about controlling the phase structure of CuInS2 were achieved by changing the ligand species or reaction temperatures. For example, Pan et al. firstly reported the synthesis of zinc blende- and wurtzite-structured CuInS2 nanocrystals by changing the ligand species , and Sudip K et al. reported the synthesis of zinc blende- and wurtzite-structured CuInS2 nanocrystals by changing the reaction temperature . We also noted that for solution-phase reactions, the pH value of reaction solution can affect the complexation capability of complexing agent to metal ions, and it might be used to the control the phase structure of products. Chai et al. has reported the synthesis of cubic and hexagonal phase ZnIn2S4 by adjusting the pH value of the reaction solution . This method presents a simple and eco-friendly way for the controlled synthesis of ternary nanomaterials with tailored structures.
On the other hand, CuInS2 in nanophase is usually synthesized in harsh conditions of high temperature and high pressure using organic solvent, which inevitably makes the reaction more difficultly controlled. In this report, we demonstrate the successful synthesis of chalcopyrite phase and wurtzite phase CuInS2 by a simple water-bath method at relatively low temperature of 80°C under atmospheric environment. By using deionized water as the solvent and thioglycolic acid as the complexing agent, the phase transformation of CuInS2 from chalcopyrite phase to wurtzite phase can be achieved by simply adjusting the pH value of the reaction solution as well as the annealing temperature. It has been found that CuInS2 gradually transformed from chalcopyrite to wurtzite with the increase of pH value, and the wurtzite CuInS2 gradually transformed to chalcopyrite phase with the increase of annealing temperature. To the best of our knowledge, this is the first report that controls the phase transformation of CuInS2 from chalcopyrite to wurtzite by adjusting the pH value of the reaction solution. This work may provide a feasible reference for the simple and easy synthesis of different phase-structured I-III-VI2 ternary semiconductor compounds.
All chemicals were used as received without further purification. Copper (II) chloride dihydrate (CuCl2 · 2H2O ≥ 99.0%), indium (III) sulfate anhydrous (In2(SO4)3 ≥ 99.99%), sodium sulfide nonahydrate (Na2S · 9H2O), and sodium hydroxide (2 mol/L NaOH solution) were all purchased from Tianjin Kermel Chemical Reagent Co. Ltd. (Tianjin, China). Thioglycolic acid (TGA) was obtained from Sinopharm Chemical Reagent Co. Ltd. (Shanghai, China). The water used in all experiments was obtained from a Millipore Milli-Q purification system and had a resistivity higher than 18.2 MΩ · cm. All experiments were carried out in water-bath pot under atmosphere.
Synthesis of CuInS2 nanoparticles
CuInS2 was synthesized in aqueous solution via a water-bath approach. In a typical synthesis, 1 mmol CuCl2 and 0.5 mmol In2(SO4)3 were mixed with 20 mL of deionized water, then TGA aqueous solution as reducing and complexing agent (20 mmol TGA in 10 mL of deionized water) was added into the solution under constant stirring. The mixture became milky white quickly. Then, the pH value of the mixed solution was adjusted from 1.27 to 10.3 by adding aqueous NaOH solution (2 mol/L) to check the effects of pH value on the final product. Na2S aqueous solution as sulfur source (2 mmol Na2S was dissolved in 10 mL of deionized water) was then added to the mixture. After stirring for 30 min, the reaction mixture was heated to 80°C for 48 h under atmosphere conditions. Finally, the obtained solution was cooled down to room temperature. The precipitate was separated by centrifugation and washed several times with deionized water and anhydrous ethanol then dried at 60°C for 8 h.
The phase and crystallographic structure of the prepared products were characterized by X-ray diffraction on a Bruker D8 Advance X-ray powder diffractometer (XRD) with Cu Kα radiation source (λ = 0.15418 nm). Scanning electron microscopy (SEM) images were acquired using a FEI Nova NanoSEM 450 scanning electron microscope (FEI, Hillsboro, OR, USA). Transmission electron microscopy (TEM) images were performed on a JEOL JEM-2010 electron microscope (JEOL, Akishima-shi, Tokyo, Japan) operating at 200 kV. X-ray photoelectron spectroscopy (XPS) analysis was performed with a Kratos Axis Ultra system using monochromatic Al Kα X-rays (1,486.6 eV). The UV-vis absorption spectra were obtained by using UV-vis Spectrometer (Perkin-Elmer, Lambda 950, Waltham, MA, USA). The simulated crystal structures and wurtzite XRD patterns of CuInS2 were obtained by using Diamond 3.2 programs.
According to Pearson’s Hard-Soft Acid-Base (HSAB) theory , a soft acid and a soft base bind more tightly than a soft base and a hard acid. Cu+ is a soft acid, In3+ is a hard acid, and the TGA is a soft base which will react preferentially with soft acid Cu+ . The Cu-SR bond should be stronger than the In-SR bond [12,18]. Therefore, the excess of TGA can balance the reaction rate between Cu+ and In3+ and S2−.
From the phenomenon of the reaction process (Additional file 1: Figure S1). When the TGA is added into the mixture solution of Cu and In ions, the color of the solution changes from blue to creamy white, which indicates that CuIn(SR) x complex is generated in the solution. If the Na2S was directly added into the solution without adjusting the pH value of the solution (pH = 1.27), the color of the solution will change from creamy white to orange. However, if the pH value of the solution was adjusted to alkalinity (pH = 10.3), the creamy white solution will become a colorless transparent solution. When we add the Na2S into the solution, the color of solution becomes gray black.
From the phenomenon of the reaction process (Additional file 1: Figure S1), It can be found that the pH value of reaction solution indeed plays an important role in the reaction. The essence is that the pH value of solution influences on the complexation of TGA. The Cu2+ can be quickly reduced to Cu+, and the CuIn(SR) x complex (creamy white) is formed when the TGA is added into the mixed solution of Cu2+ and In3+, which makes the solution change from blue to creamy white because the Cu2+ is blue but Cu+ is colorless. As the pH value increases with the addition of NaOH, the CuIn(SR) x complex dissociates and releases Cu+ into solution, and the solution changes from a creamy white to a colorless transparent solution. In this case, the Cu2S will be easily generated when Na2S is added into the solution, which makes the mixed solution change from a colorless transparent to a gray black solution. From the XRD pattern of the as-grown products of the gray black solution (Additional file 1: Figure S2), the peaks can be well indexed to (220) and (311) planes of Cu2S (JCPDS card file no. 02-1287), respectively, proving the formation of Cu2S. It is the emergence of Cu2S that leads to the formation of wurtzite CuInS2. Both Cu2S and wurtzite CuInS2 have a hexagonal structure; such a structural similarity induces the formation of wurtzite CuInS2 [1,19].
A series of comparative experiments have also been carried out. In any case, the pH is adjusted in the solution without TGA; the chalcopyrite nor wurtzite CuInS2 can be synthesized. The synthesized products both in the acidic and alkaline environment are CuS (JCPDS card file no. 06-0464) and In(OH)3 (JCPDS card file no. 76-1464) (Additional file 1: Figure S3). It is due to the reason that the Cu2+ cannot be reduced to Cu+ in the solution in the absence of TGA, and CuS is generated when the Na2S is added. Simultaneously, Na2S is a strong alkaline compound; as a result, In(OH)3 is also formed. The comparative experiment also indicates that TGA plays a crucial role for the formation of CuInS2 because of its complexation and reducibility [20,21].
In summary, CuInS2 in chalcopyrite and wurtzite phases has been successfully synthesized via a low-cost, facile water-bath method. The phase structure of as-synthesized CuInS2 can be easily controlled by adjusting the pH value of the reaction solution. Low-cost thioglycolic acid plays a key role in the synthesis process of CuInS2. Thioglycolic acid acts not only as a stabilizer and complexing agent to balance the reaction rate among Cu+, In3+, and S2− but also as a reducing agent which can reduce Cu2+ to Cu+. Compared with the traditional organic phase synthesis route, this method provides a feasible way that is much simpler, greener, and cheaper, in addition to the easy control of phase structure for the mass production of CuInS2.
This work was supported by the National Natural Science Foundation of China (nos. 20371015, 10874040, 20903034, and 21203055), the Cultivation Fund of Key Scientific and Technical Innovation Project, Ministry of Education of China (no. 708062), Basic and Frontier Research Program of Science and Technology Department of Henan Province (no. 112300410277), and the Program for Changjiang Scholars and Innovative Research Team in University (no. PCS IRT1126). BBH and BBX contributed equally to this paper.
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