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Effects of the Cu Ion on the Structural and Optical Properties of Yttrium Doped ZnO by Solution Combustion

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DOI: 10.4236/wjcmp.2017.74008    539 Downloads   902 Views  


In this experiment, pure, Y3+ doped ZnO and Cu2+ + Y3+ co-doped ZnO were synthesized by a solution combustion method. The Y3+ dopant concentration was fixed in 3%wt. and the Cu2+ dopant concentrations were 0, 1, 2, 3, 10, and 20%wt. The XRD spectra showed that the original hexagonal wurtzite structure of ZnO is conserved after doping process, an increasing red shift until 10%wt. Cu2+ doping and decrease at higher Cu2+ doping and also, the chemical creation of the news Y2O3 and Y2Cu2O5 phases. The behavior of the photoluminescence of the samples as a function of Cu2+ doping reveal that the green emission band of the ZnO is quenching and the ZnO UV emission intensity decrease notably for all Cu2+ doping. The scanning electron microscope analysis of the Cu2+ + Y3+ co-doped ZnO samples reveal the existence of grains agglutinated forming like-spheres particles. However, the nano-sized characteristic of the crystals is confirmed.

1. Introduction

The zinc oxide (ZnO) is one of the oldest n-type semiconductor material studied, and is actually a promising material in fundamental studies and technological applications due to its varied and outstanding properties such as: high conductance and transparence in thin films, chemical and thermal stability, wide band gap (3.37 eV) and a large exciton binding energy (60 meV) [1] , which presents efficient photoluminescence and thermo-luminescence in intrinsic state [2] . The property that has the ZnO of can be doped opened a lot of technological applications: doping of ZnO for fabricating semiconductor devices such as vacuum fluorescent displays, field emission displays [3] , solar cells [4] , magnetic [5] , photoluminescent [6] , electro-optical [7] , etc. The ZnO can be synthesized by various methods, such as electrodeposition [8] , evaporation [9] , vapor-liquid-solid (VLS) growth [10] , metal-organic catalyst, assisted vapor-phase epitaxy [11] , aqueous thermal decomposition [12] , microwave activated chemical bath deposition (MW-CBD) [13] , chemical bath deposition (CBD) [14] , surfactant-assisted hydrothermal method [15] , and solution combustion method [16] [17] . This last method is more convenient than other because it is pensive, it has an easier composition control, and coating can be deposited on large area etc. Co-doping of host matrix is a technique for incorporating two or more elements into a host lattice with the objective of change sum or improves the properties physical and chemical of the host matrix. The ZnO has been co-doped with various elements (rare earth, lanthanides, metals, etc.) combined [2] [3] [4] , in special with Cu2+ ions to tailoring the optical properties of Y3+ doped ZnO compounds because the Cu2+ ion has the capacity of: modify the luminescence of ZnO crystals by creating localized impurity levels [9] [18] . But also the Cu2+ ion can quench some emission photoluminescence type [19] as will be showed in this study. However, the doping of ZnO with Cu2+ ions cannot modify ZnO structure [20] . In turn, the Y3+ element belong to rare earth periodic family [5] [6] , the importance of Y3+ is its capacity for tailoring the optical properties of ZnO, because Y3+ doping decrease the energy band gap of ZnO [7] . The Y3+ surface hinders crystalline growth and promotes vacancies generation [21] . In this experiment, the possible effects caused by the Cu2+ ions on the structural and optical properties of Y3+ doped ZnO compounds are analyzed and explicated. The Cu2+ + Y3+ co-doping process is realized by a solution combustion technique.

2. Experimental Details

2.1. The Solution Combustion Method

The experimental method of chemical synthesis solution combustion [17] , is quite simple, fast and economical in which an oxidizer and a fuel agents are combined in a highly exothermic red-ox chemical reaction stoichiometric, producing ZnO, H2O (vapor), molecular N2, and CO2. In this work using Zinc Nitrate hexahydrate [Zn(NO3)2∙6H2O] as oxidizer, urea [(H2NCONH2)] as fuel, yttrium chloride [YCl3] and copper chloride [CuCl2] as dopants, undoped and Cu2+ + Y3+ doped ZnO were synthesized by a solution combustion technique as a function of Cu2+ ion concentration in %wt, maintaining the Y3+ concentration constant in 3%wt. The samples were later annealed at 835˚C by 2 h.

2.2. Stoichiometric Equation

Pure and Cu2+ + Y3+ doped ZnO samples were obtained by a solution combustion technique by means of the following redox chemical reaction stoichiometric:

3Zn ( NO 3 ) 2 × 6H 2 O + 5H 2 NCONH 2 + 2 ( YCl 3 + CuCl 3 ) 3ZnO + 10H 2 O + 5CO 2 + 8N 2 + 2 ( Cu 2+ + Y 3+ ) + 5Cl 2 (1)

The Equation (1) was obtained by taken into account the oxidizer/fuel molar radio (O/F = 1) required for a stoichiometric mixture which is determined by summing the total oxidizing and reducing valences in the oxidizer compound and dividing it by the sum of the total oxidizing and reducing valences in the fuel compound [17] . Accordingly for the complete combustion of zinc nitrate-urea mixture, the molar ratio becomes 5/3, the equation balanced (1) was obtained with this value ratio. Using the weight atomic concept in Equation (1), it was used to obtain 3 gr. of ZnO for all the Cu2+ ion concentrations. The dopants yttrium and copper by means its respective chloride were simultaneously integrated into ZnO host in each combustion reaction using the dopants concentrations correct. The samples produced were characterized by x-ray diffraction technique using a Philips PW 1800 diffractometer using Cu Kα radiation, the morphology of the samples was studied by means of a scanning electron microscopy JEOL JSM 840 A , and the photoluminescence spectra was recorded using a Tektronix 792 AD.

3. Results and Discussion

3.1. X-Ray Diffraction (XRD) Study

The XRD patterns of Y3+ doped ZnO with 3%wt. and Cu2+ + Y3+ co-doped ZnO with 3%wt. of Y3+ ion and 1, 3, 5, 10, and 20%wt. of Cu2+ ion concentrations and after annealed at 835˚C by 2 h are showed in Figure 1. The observed XRD characteristic peaks positioned in 2θ scale at 31.64, (100), 34.32, (002), 36.02, (101), 47, 45, (102), 56.49, (110), 62.70, (103), 66.30, (201), 67.85, (112) and 69.93, (201) shows the good crystallinity of the material. All the diffraction peaks can be indexed to the hexagonal wurtzite structure of ZnO (JCPDS card No. 36-1451, a = b = 3.249A, c = 5.206A). However, other characteristic peaks at 29˚, (222) and 27˚, (230), corresponding to the yttrium oxide (Y2O3) and Y2Cu2O5 phases respectively also were observed in Cu2+ + Y3+ co-doped ZnO, which can be attributed to the doping of Y3+ ion into Zn2+ lattice site. Also, it is observed that the peak intensity of the news phases decrease with Cu2+ ion concentration until total quenching at 20%wt. due to Cu2+ ion incorporation into Zn-Y-O lattice site and segregation of Y3+ ion toward ZnO surface. The Y2Cu2O5 phase also is obtained as secondary phase in the YBaCuO superconductor synthesis [22] [23] [24] [25] . The Figure 2 shows a magnification of the (002) plane between 34.1˚ and 34.7˚ in which are observed the changes in peak intensity and peak position as a function of Cu2+ ion concentration. The peak intensity is increased when the Cu2+ ion is incorporated into Y3+-Zn-O lattice until 10%wt. Cu2+ ion concentration. This is attributed to the Cu2+ interstitial existence sharing the

Figure 1. XRD patterns of Y3+ doped (3%wt.) ZnO and Cu2+ + Y3+ co-doped ZnO as a function of Cu2+ ion concentration in %wt.

Figure 2. Red shift of the (002) enlarged plane as a function of Cu2+ ion concentration in %wt.

oxygen with the Zn2+ atoms increasing the peak intensity. After 10%wt. the peak intensity decrease, due to excess of Cu2+ atoms that are energetically efficient to coalesce into metallic copper cluster decreasing the peak intensity [20] . The peak position along (002) plane of Cu2+ + Y3+ co-doped ZnO samples is red shifted in 2θ scale and broader up to 10%wt. Cu2+ ion concentration, after this value the peak position is increased newly due to the effect by intercalation of Cu2+ ion on the interatomic distance of the Y-Zn-O lattice [20] . The average crystal size of the samples was obtained from diffraction (101) plane using the Debye-Scherrer equation:

D = 0.9 λ β cos θ (2)

where λ is the X-ray wavelength used (1.5406Å), β is the full width at half maximum (FWHM) along (101) plane and theta is the Bragg diffraction angle. The Figure 3(a) and Figure 3(b) shows the change in FWHHM and average crystal


Figure 3. (a) FWHM; (b) average crystal size, as a function of Cu2+ ion concentration in %wt.

size as a function of Cu2+ ion concentration respectively, it is observed from Figure 3(a) that the FWHM increases with Cu2+ ion concentration until reach a maximum value at 10 %wt., after this value decrease until reach a value minimum. In contrary, from Figure 3(b) it is observed that the crystal size decrease with the Cu2+ ion concentration until reach a minimum value in 10%wt. after this value the crystal size increase. This behavior between the FWHM and the average crystal size is predicted by the Debye-Scherrer equation, since for a maximum value of FWHM correspond a minimum value in crystal size. Also it is observed that the Cu2+ + Y3+ co-doped ZnO crystals have less size than Y3+ doped ZnO; the initial reduction size from 75 nm with 0.0%wt. of Cu2+ ion to 40 nm whit 10%wt. of Cu2+ ion is due to the distortion produced by Cu2+ ions intercalated in the Zn-Y-O lattice [20] . At higher Cu2+ concentration than 10%wt. the Cu2+ atoms excess is combined forming the Y2Cu2O5 compound.

3.2. Photoluminescence Study

The Figure 4 shows the photoluminescence (PL) spectra of pure ZnO and Y3+ doped ZnO with 3%wt. The spectra were obtained in the UV-Vis range, illuminated with an excitation wavelength of 350 nm at room temperature. The PL spectrum of pure ZnO samples, exhibits the typical main band with characteristics peaks centered about 390 nm and corresponds to the near band edge (NBE) emission [6] . At higher wavelengths than NBE diffraction peak appears with less intensity that NBE peak the green emission band centered about 518 nm and attributed to free exciton recombination. From Figure 4 can be observed and calculated a little blue shift when Y3+ dopant was incorporated into ZnO host lattice, changing the ultra-violet NBE emission from 390 to 382 nm increasing the ZnO band gap in 0.3 eV. This slight blue shift of the UV peak is caused by 3%wt. Y3+ doping [9] and [16] . However it is observed an increase in UV intensity in Y3+ doped ZnO compared with UV intensity of pure ZnO. The Figure 5 exhibit the room temperature PL spectra of Cu2+ + Y3+ co-doped ZnO samples with var-

Figure 4. Photoluminescence spectrum of pure ZnO and doped ZnO with 3%wt. Y3+ ion. The samples were illuminated using a wavelength excitation of 350 nm.

Figure 5. Photoluminescence spectra of Cu2+ + Y3 co-doped ZnO as a function of Cu2+ ion concentration in %wt.

ious Cu2+ ion concentrations values of 2, 3, 5, 10 and 20%wt., it is clearly observed that for all Cu2+ concentration the green PL emission due to free exciton recombination has been quenched by the intercalation of Cu2+ ions into Y3+ + ZnO host lattice; this quenching effect is attributed to a non-radiative recombination process known as non-radiative recombination Auger phenomena which is associated to degenerate electrons, in which the energy released by an electron is immediately recombined and absorbed by another electron and the energy involved is dissipated by phonons. Auger process is considered as the cause major of non-radiative recombination in semiconductor materials. Auger process depends on the doping atoms concentration and defects in the lattice. [19] . However, in Fig. 5 also it is observed that the UV-NBE emission of the samples is diminished by increasing Cu2+ ion concentration, indicating that the optical-gap of ZnO semiconductor can be tailored by means of Cu2+ doping. This last result can be technologically applied in UV radiation sensors fabrication [26] .

3.3. Morphology Study

The scanning electron microscope (SEM) technique has been used to observe the surface morphology (SM) of the particles. The Figures 6(a)-(d) exhibits the SEM images of the SM of Cu2+ + Y3+ co-doped ZnO. The Figure 6(a) shows the SM of Y3+ doped ZnO sample, it presents the existence of like-ovoid particles compact, dense structure and forming layers which have its surface covered with grains of size similar that are unevenly distributed. The average size grain is of 30 nm. The Figure 6(b) shows the SM of Cu2+ + Y3+ co-doped ZnO with 2%wt. of Cu2+ ions concentration, it is observed that the grains are most agglomerated

Figure 6. Surface morphology of Cu2+ + Y3+ doped ZnO as a function of Cu2+ ion concentration in %wt. and 3% of Y3+ fixed.

and evenly distributed in the sample. In this case the grains have an average size of 50 nm. The Figure 6(c) exhibits the SM of the Cu2+ + Y3+ co-doped ZnO with 3%wt. of Cu2+ ions concentration. It is seen that further increase in the intercalation of Cu2+ ions into Zn-Y-O host lattice improves the crystallinity of the sample. The Figure 6(c) displays the SM of Cu2+ + Y3+ co-doped ZnO with 3%wt. of Cu2+ ions, the particles presents like-spheres form and higher size than Y3+ doped ZnO. The average grain size of these particles is 50 nm. Finally the Figure 6(d) exhibits the SM of Cu2+ + Y3+ co-doped ZnO with 10%wt. of Cu2+ ions concentration. In this Cu2+ concentration level is observed the presence of the Y2Cu2O5 as is corroborated by the XRD patterns showed in Figure 1. However, also can be seen Cu2+ ions interstitial localized into ZnO matrix. The geometry of these particles is like-spheres with an average size of 75 nm.

4. Conclusion

In this study, pure and Cu2+ + Y3+ co-doped ZnO were synthesized as a function of Cu2+ ion concentration by a solution combustion method. The XRD study showed that the hexagonal wurtzite structure of ZnO is maintained after Cu2+ doping process. Using the (002) plane of XRD spectra, a red shift was observed due to Cu2+ doping process. The PL results for Y3+ doped ZnO showed a UV intensity higher compared with the UV intensity of pure ZnO. For all the Cu2+ ion concentrations, the green PL emission is quenching by Cu2+ doping effect. The UV PL emission can be tailored by Cu2+ doping effect. In 10%wt. of Cu2+ doping, the Y2Cu2O5 phase is created. A blue shift of 0.3 eV is observed in the UV PL emission of Cu2+ + Y3+samples due to Cu2+ doping effect.


The authors wish to thank to Dr. Ciro Falcony (IPN), Adriana Tejeda (IIM) for the XRD measurements, to Omar Novelo Peralta (IIM) for his SEM study, to M.A. Canseco Martinez (IIM) for their chemical analysis.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

López-Romero, S. , Quiroz-Jiménez, M. , García-Hipólito, M. and Aguilar-Castillo, A. (2017) Effects of the Cu Ion on the Structural and Optical Properties of Yttrium Doped ZnO by Solution Combustion. World Journal of Condensed Matter Physics, 7, 89-98. doi: 10.4236/wjcmp.2017.74008.


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