Open Access
1 January 2011 Cu2ZnSnS4 polycrystalline thin films with large densely packed grains prepared by sol-gel method
Minlin Jiang, Yong Li, Rabin Dhakal, Prem S. Thapaliya, Michael A. Mastro, Joshua Caldwell, Fritz J. Kub, Xingzhong Yan
Author Affiliations +
Abstract
Cu2ZnSnS4 (CZTS) was obtained from a sol-gel precursor which consists of copper chloride, zinc chloride, tin chloride, and thiourea. CZTS thin films were prepared by spin-coating the sol-gel precursor followed by annealing in a nitrogen atmosphere. The morphology, composition, and structure of the absorber layer were studied by scanning electron microscopy, energy dispersive spectroscopy, x-ray diffraction, and Raman scattering. The optical measurement shows the bandgap of these films is ∼1.51 eV, and the optical absorption coefficient is on the order of 104 cm−1. CZTS solar cells with a structure of low-alkali glass/Mo/CZTS/CdS/i-ZnO/ZnO:Al/Al grid were tentatively fabricated. The best solar cell showed a short-circuit current density of 5.06 mA/cm2, an open-circuit voltage of 358 mV, a fill factor of 34.66%, and an efficiency of 0.63% under AM1.5 (100 mW/cm2) illumination. These results demonstrate the CZTS thin films were successfully deposited by a cheap sol-gel technique.

1.

Introduction

Research on thin film photovoltaic (PV) technologies, such as CdTe and Cu(In,Ga)(S,Se)2 (CIGS), have recently made tremendous progress academically1 and industrially.2 It was claimed by First Solar that manufacturing costs ranging from $0.59/W to $0.62/W has already been realized at the end of 2009.3 However, the scarcity and toxicity of raw materials will become obstacles for CdTe and CIGS to significantly snatch PV market share from dominant silicon wafer-based PV technologies. Kesterite Cu2ZnSnS4 (CZTS) has gained broad interest due to its abundant raw materials and semiconductor properties comparable to chalcopyrite CIGS.4, 5, 6, 7

Several methods have been employed to deposit CZTS thin films. These include direct current/radio-frequency magnetron sputtering deposition,8 thermal evaporation,9 electron beam evaporation,10 spray pyrolysis deposition,11 sol-gel deposition,12 electrodeposition,13 photochemical deposition,14 pulsed laser deposition,15 screen-printing,16 and nanoparticle-based method.17 Katagiri reported a promising conversion efficiency of 6.77% in 2008 CZTS thin film solar cell (TFSC) which was fabricated by sputtering elements and metal sulfides followed by annealing in H2S.18 In 2010, IBM slightly improved the efficiency to 6.81% using a co-evaporation process.19 However, the high vacuum employed by both teams requires expensive equipment, complicated operations, and significant maintenance. It is generally promoted that nonvacuum deposition techniques are to manufacture low-cost PV modules.

In this work, we report on a different route, using sol-gel as CZTS precursors. In this process, the CZTS polycrystal thin films were deposited on soda lime glass and low-alkali glass substrates by the spin-coating of CZTS sol-gel followed by annealing in nitrogen atmosphere. Densely packed crystal domains were observed with these annealed films. Results from absorber and device characterization demonstrated the feasibility to fabricate a CZTS PV device by an inexpensive sol-gel process.

2.

Experimental Procedures

Copper chloride (2 M), zinc chloride (1.2 M), tin chloride (1 M), and thiourea (8 M) were added in a mixture solvent water/ethanol (v/v 70:30). Clear yellow sol-gel was formed after being stirred at room temperature for tens of minutes. The spin-coating process was used to deposit CZTS sol-gel on substrates. Solvents in the as-coated films were removed by drying at 110°C. Preannealing at 250°C was employed in nitrogen to decompose CZTS precursors for generating metal sulfides (copper sulfide, zinc sulfide, and tin sulfide) nanocrystals.20 The spin-coating and drying processes as well as preannealing were repeated twice to deposit relatively thick CZTS thin films (>2 μm). Finally, the annealing temperature was elevated to 550°C for growing polycrystalline CZTS thin films.

The optical property of the prepared thin films was examined by a UV-visible-infrared spectrophotometer. Surface and cross section morphologies of CZTS thin films were investigated using scanning electron microscopy (SEM). The composition of the films was analyzed by energy-dispersive x-ray spectroscopy (EDX). X-ray diffraction (XRD) spectrum and room temperature Raman spectrum were recorded to examine the crystal structure.

3.

Results and Discussion

Figure 1 shows the SEM surface image of a CZTS film preannealed at 250°C. Due to volume contraction arising from the evaporation of volatile products, cracks exist in the film. Organic binders in the CZTS precursor sol-gel could prevent the formation of cracks.21 The grain boundaries are difficult to be delineated because a preannealed sample is mainly composed of nanoparticles of metal sulfides (copper sulfide CuxS, zinc sulfide ZnxS, and tin sulfide SnxS). These sulfides react to form a CZTS nanocrystal during heating. High temperature annealing could improve the crystallinity and increase the grain size of thin films.22 Moreover, the efficiency of TFSC increases with increasing crystal size of the absorber layers.22 A CZTS thin film containing large densely packed grains with size of more than 400 nm was achieved after annealing at 550°C in nitrogen atmosphere [Fig. 1]. The cross section images of a CZTS thin film are shown in Figs. 1 and 1. The thickness of a CZTS thin film is decreased by ∼200 nm after the annealing process in comparison to a preannealed thin film. This was attributed to nanocrystals congregation at high temperature for forming larger crystalline domains.

Fig. 1

SEM images of CZTS films (a) surface after preannealing, (b) cross section after preannealing, (c) surface after annealing, and (d) cross-section after annealing.

019501_1_1.jpg

The compositional ratios of Cu/(Zn+Sn), Zn/Sn, and S/metals examined by EDX are shown in Table 1. A preannealed CZTS film is copper-poor, zinc-rich, and slightly sulfur-poor, which are beneficial to prevent the formation of binary phases such as Cu2S, and to induce self-doped p-type conductivity.23 A minute quantity of chlorine remained after preannealing and was totally removed after annealing. The preannealing process could fully remove carbon as a form of carbon dioxide. As verified by EDX results, a loss of Sn was recorded during annealing at higher temperature. Similar phenomena was observed by Weber who suggested that a CZTS thin film should be deposited at a temperature lower than 550°C to suppress the evaporation of tin sulfide.24 It remains unresolved to what extent loss of tin could be endured without detrimental effects on CZTS TFSC since CZTS TFSCs have been successfully fabricated with a large variation of composition.19 Moreover, the versatility of the sol-gel method provides a simple way to optimize the composition which can be fine-tuned by changing the molar concentration of reagents when preparing the CZTS sol-gel precursor.

Table 1

Chemical composition of the CZTS films.

Mass percentage (%)Atomic percentage
CuZnSnSClCCu/(Zn+Sn)Zn/SnS/(Cu+Zn+Sn)
Preannealing26.3817.8028.2827.070.4700.811.150.91
Annealing24.6819.8225.2030.29000.751.431.05

Figure 2 shows an XRD pattern of a CZTS film annealed at 550°C. All peaks can be assigned to kesterite CZTS.25 The phenomenon of three strong peaks is attributed to the polycrystallinity of a deposited CZTS thin film. Three continuous strong peaks were also observed by Lu on as-synthesized wurtzite CZTS nanocrystals.26 The existence of CZTS is further confirmed by the presence of Raman peaks at 256 to 257 cm−1, 288 cm−1, and 338 to 339 cm−1. These are in good agreement with the reported data.27, 28 From both the elemental and structural analysis, a total reaction, 2CuCl2 + ZnCl2 + SnCl2 + 4SC(NH2)2 + 8H2O → Cu2ZnSnS4 + 4CO2 + 8NH4Cl, may be suggested to the presented process.

Fig. 2

(a) XRD pattern and (b) Raman spectrum of CZTS film annealed at 550°C.

019501_1_2.jpg

Figure 3 shows the optical transmittance of CZTS thin films preannealed at 250°C and annealed at 550°C. It is reported that CuxS, SnxS, and ZnxS have direct bandgap of 2.35 eV,29 2.0 eV,30 and 2.99 to 3.80 eV,31 respectively, all of which are larger than that of CZTS.8 Therefore, the transmittance of an annealed CZTS thin film was observed with redshift. The optical absorption coefficient is approximately derived from the transmittance data and shown in Fig. 3 as a function of photon energy. The absorption coefficient is larger than 104 cm−1 in the photon energy range greater than 1.2 eV, which agrees well with those reported in literature.11, 32, 33

Fig. 3

(a): Transmittance of CZTS films and (b) absorption coefficient of CZTS film annealed at 550°C.

019501_1_3.jpg

The insert in Fig. 3 shows the square of the product of the absorption coefficient and photon energy (hν) as a function of the photon energy. The bandgap is estimated to be 1.51 eV by extrapolating the straight line part of the (αhν)2 versus hν curve to the intercept of the horizontal axis as depicted in Fig. 3. This value is quite close to the theoretical optimal value for a single-junction solar cell.34 From the perspective of optical properties, the CZTS film deposited using spin-coating of sol-gel followed by annealing can be considered a suitable photovoltaic material.

CZTS solar cells with an active area of 0.46 cm2 were fabricated and characterized. All cell parameters were relatively low. The current density-voltage (J-V) characteristic of the best solar cell is presented in Fig. 4. The performance parameters were as follows: a short circuit current density (Jsc) of 5.06 mA/cm2, an open-circuit voltage (Voc) of 358 mV, a fill factor of 34.66%, and an efficiency (η) of 0.63% under simulated AM1.5 illumination. Shunt and series resistances, Rsh and Rs, were 99.78 and 31.30 Ω·cm2, respectively, which caused the quite low fill factor.

Fig. 4

J–V characteristic of the best CZTS solar cell.

019501_1_4.jpg

4.

Conclusions

CZTS thin film was successfully deposited by a sol-gel method. The annealed film showed large densely packed grains. This film possesses a high optical absorption coefficient and optical bandgap near to the ideal bandgap of the absorber for single junction solar cells. The film could be a suitable photovoltaic material from the perspective of optical properties. Desired composition was achieved for the CZTS thin film after preannealing at low temperature. Loss of tin was observed after annealing at higher temperature, as should be solved for high-performance TFSCs. The best solar cell showed a low conversion efficiency of 0.63%. Optimization experiments are in progress and expected to lead to a significant improvement.

Acknowledgments

We acknowledge the financial support from the NASA EPSCoR through Contract NNX09AU83A and SDSU EE PhD program. We are also grateful to OPTORUN Co. Ltd. (Japan) for providing Mo-coated low-alkali glass substrates for this project.

References

1. 

P. Jackson, D. Hariskos, E. Lotter, S. Paetel, R. Wuerz, R. Menner, W. Wischmann, and M. Powalla, “New world record efficiency for Cu(In,Ga)Se2 thin-film solar cells beyond 20%,” Prog. Photovoltaics, (2011) http://dx.doi.org/10.1002/pip.1078 Google Scholar

2. 

SOLAR FRONTIER (2011, April 20). Solar Frontier Officially Opens World's Largest CIS Solar Module Plant, http://www.solar-frontier.com/MainMenu/News/19 Google Scholar

3. 

M. A. Green, “Learning experience for thin-film solar modules: First Solar Inc. case study,” Prog. Photovoltaics, 19 (4), 498 –500 (2010). http://dx.doi.org/10.1002/pip.1057 Google Scholar

4. 

S. H. Han, F. S. Hasoon, H. A. Al-Thani, A. M. Hermann, and D. H. Levi, “Effect of Cu deficiency on the optical properties and electronic structure of CuIn1-xGaxSe2,” J. Phys. Chem. Solids, 66 1895 –1898 (2005). http://dx.doi.org/10.1016/j.jpcs.2005.10.112 Google Scholar

5. 

O. Lundberg, M. Bodegard, J. Malmstrom, and L. Stolt, “Influence of the Cu(In,Ga)Se2 thickness and Ga grading on solar cell performance,” Prog. Photovoltaics, 11 77 –88 (2003). http://dx.doi.org/10.1002/pip.462 Google Scholar

6. 

H. Katagiri, K. Jimbo, W. S. Maw, K. Oishi, M. Yamazaki, H. Araki, and A. Takeuchi, “Development of CZTS-based thin film solar cells,” Thin Solid Films, 517 2455 –2460 (2009). http://dx.doi.org/10.1016/j.tsf.2008.11.002 Google Scholar

7. 

H. Katagiri, “Cu2ZnSnS4 thin film solar cells,” Thin Solid Films, 480–481 426 –432 (2005). http://dx.doi.org/10.1016/j.tsf.2004.11.024 Google Scholar

8. 

H. Yoo and J. Kim, “Comparative study of Cu2ZnSnS4 film growth,” Sol. Energy Mater. Sol. Cells, 95 239 –244 (2011). http://dx.doi.org/10.1016/j.solmat.2010.04.060 Google Scholar

9. 

B. Schubert, B. Marsen, S. Cinque, T. Unold, R. Klenk, S. Schorr, and H. W. Schock, “Cu2ZnSnS4 thin film solar cells by fast coevaporation,” Prog. Photovoltaics, 19 93 –96 (2010). http://dx.doi.org/10.1002/pip.976 Google Scholar

10. 

H. Katagiri, K. Saitoh, and T. Washio, “Development of thin film solar cell based on Cu2ZnSnS4 thin films,” Sol. Energy Mater. Sol. Cells, 65 141 –148 (2001). http://dx.doi.org/10.1016/S0927-0248(00)00088-X Google Scholar

11. 

Y. B. Kumar, P. U. Bhaskar, G. S. Babu, and V. S. Raja, “Effect of copper salt and thiourea concentrations on the formation of Cu2ZnSnS4 thin films by spray pyrolysis,” Phys. Status Solidi A, 207 149 –156 (2010). http://dx.doi.org/10.1002/pssa.200925194 Google Scholar

12. 

K. Tanaka, M. Oonuki, N. Moritake, and H. Uchiki, “Cu2ZnSnS4 thin film solar cells prepared by non-vacuum processing,” Sol. Energy Mater. Sol. Cells, 93 583 –587 (2009). http://dx.doi.org/10.1016/j.solmat.2008.12.009 Google Scholar

13. 

J. J. Scragg, D. M. Berg, and P. J. Dale, “A 3.2% efficient Kesterite device from electrodeposited stacked elemental layers,” J. Electroanal. Chem., 646 52 –59 (2010). http://dx.doi.org/10.1016/j.jelechem.2010.01.008 Google Scholar

14. 

K. Moriya, K. Tanaka, and H. Uchiki, “Characterization of Cu2ZnSnS4 thin films prepared by photo-chemical deposition,” Jpn. J. Appl. Phys., 44 715 –717 (2005). http://dx.doi.org/10.1143/JJAP.44.715 Google Scholar

15. 

K. Moriya, K. Tanaka, and H. Uchiki, “Cu2ZnSnS4 thin films annealed in H2S atmosphere for solar cell absorber prepared by pulsed laser deposition,” Jpn. J. Appl. Phys., 47 602 –604 (2008). http://dx.doi.org/10.1143/JJAP.47.602 Google Scholar

16. 

Z. Zhou, Y. Wang, D. Xu, and Y. Zhang, “Fabrication of Cu2ZnSnS4 screen printed layers for solar cells,” Sol. Energy Mater. Sol. Cells, 94 2042 –2045 (2010). http://dx.doi.org/10.1016/j.solmat.2010.06.010 Google Scholar

17. 

C. Chory, F. Zutz, F. Witt, H. Borchert, and J. Parisi, “Synthesis and characterization of Cu2ZnSnS4,,” Phys. Status Solidi C, 7 1486 –1488 (2010). http://dx.doi.org/10.1002/pssc.200983217 Google Scholar

18. 

H. Katagiri, K. Jimbo, S. Yamada, T. Kamimura, W. S. Maw, T. Fukano, T. Ito, and T. Motohiro, “Enhanced conversion efficiencies of Cu2ZnSnS4-based thin film solar cells by using preferential etching technique,” Appl. Phys. Express, 1 041201 (2008). http://dx.doi.org/10.1143/APEX.1.041201 Google Scholar

19. 

K. Wang, O. Gunawan, T. Todorov, B. Shin, S. J. Chey, N. A. Bojarczuk, D. Mitzi, and S. Guha, “Thermally evaporated Cu2ZnSnS4 solar cells,” Appl. Phys. Lett., 97 143508 (2010). http://dx.doi.org/10.1063/1.3499284 Google Scholar

20. 

N. Nakayama and K. Ito, “Sprayed films of stannite Cu2ZnSnS4,” Appl. Surf. Sci., 92 171 –175 (1996). http://dx.doi.org/10.1016/0169-4332(95)00225-1 Google Scholar

21. 

T. Todorov and D. B. Mitzi, “Direct liquid coating of chalcopyrite light-absorbing layers for photovoltaic devices,” Eur. J. Inorg. Chem., 2010 (1), 17 –28 (2010). http://dx.doi.org/10.1002/ejic.200900837 Google Scholar

22. 

L. Zhang, Q. He, W. Jiang, F. Liu, C. Li, and Y. Sun, “Effects of substrate temperature on the structural and electrical properties of Cu(In,Ga)Se2 thin films,” Sol. Energy Mater. Sol. Cells, 93 114 –118 (2009). http://dx.doi.org/10.1016/j.solmat.2008.09.002 Google Scholar

23. 

S. Chen, J. Yang, X. Gong, A. Walsh, and S. Wei, “Intrinsic point defects and complexes in the quaternary kesterite semiconductor Cu2ZnSnS4,” Phys. Rev. B, 81 245204 (2010). http://dx.doi.org/10.1103/PhysRevB.81.245204 Google Scholar

24. 

A. Weber, R. Mainz, and H. W. Schock, “On the Sn loss from thin films of the material system Cu-Zn-Sn-S in high vacuum,” J. Appl. Phys., 107 013516 (2010). http://dx.doi.org/10.1063/1.3273495 Google Scholar

25. 

W. Schafer and R. Nitsche, “Tetrahedral quaternary chalcogenides of the type Cu2-II-IV-S4 (Se4),” Mater. Res. Bull., 9 645 –654 (1974). http://dx.doi.org/10.1016/0025-5408(74)90135-4 Google Scholar

26. 

X. Lu, Z. Zhuang, Q. Peng, and Y. Li, “Wurtzite Cu2ZnSnS4 nanocrystals: A novel quaternary semiconductor,” Chem. Commun., 47 3141 –3143 (2011). http://dx.doi.org/10.1039/c0cc05064d Google Scholar

27. 

F. Liu, K. Zhang, Y. Lai, J. Li, Z. Zhang, and Y. Liu, “Growth and characterization of Cu2ZnSnS4 thin films by DC reactive magnetron sputtering for photovoltaic applications,” Electrochem. Solid-State Lett., 13 H329 –H381 (2010). http://dx.doi.org/10.1149/1.3481764 Google Scholar

28. 

M. Grossberg, J. Krustok, J. Raudoja, K. Timmo, M. Altosaar, and T. Raadik, “Photoluminescence and Raman study of Cu2ZnSn(SexS1−x)4 monograins for photovoltaic applications,” Thin Solid Films, 519 7403 –7406 (2010). http://dx.doi.org/10.1016/j.tsf.2010.12.099 Google Scholar

29. 

H. M. Pathan, J. D. Desai, and C. D. Lokhande, “Modified chemical deposition and physico-chemical properties of copper sulphide (Cu2S) thin films,” Appl. Surf. Sci., 202 47 –56 (2002). http://dx.doi.org/10.1016/S0169-4332(02)00843-7 Google Scholar

30. 

M. Khadraoui, N. Benramdane, C. Mathieu, A. Bouzidi, R. Miloua, Z. Kebbab, K. Sahraoui, and R. Desfeux, “Optical and electrical properties of Sn2S3 thin films grown by spray pyrolysis,” Solid State Commun., 150 297 –300 (2010). http://dx.doi.org/10.1016/j.ssc.2009.10.032 Google Scholar

31. 

S. D. Sartale, B. R. Sankapal, M. Lux-Steiner, and A. Ennaoui, “Preparation of nanocrystalline ZnS by a new chemical bath deposition route,” Thin Solid Films, 480–481 168 –172 (2005). http://dx.doi.org/10.1016/j.tsf.2004.11.054 Google Scholar

32. 

P. M. P. Salome, P. A. Fernandes, A. F. da Cunha, J. P. Leitão, J. Malaquias, A. Weber, J. C. González, and M. I. N. da Silva, “Growth pressure dependence of Cu2ZnSnSe4 properties,” Sol. Energy Mater. Sol. Cells, 94 2176 –2180 (2010). http://dx.doi.org/10.1016/j.solmat.2010.07.008 Google Scholar

33. 

H. Katagiri, N. Sasaguchi, and S. Hando, “Preparation films by and evaluation of Cu2ZnSnS4 thin sulfurization of E-B evaporated precursors,” Sol. Energy Mater. Sol. Cells, 49 407 –414 (1997). http://dx.doi.org/10.1016/S0927-0248(97)00119-0 Google Scholar

34. 

T. Zdanowicz, T. Rodziewicz, and M. Zabkowska-Waclawek, “Theoretical analysis of the optimum energy band gap of semiconductors for fabrication of solar cells for applications in higher latitudes locations,” Sol. Energy Mater. Sol. Cells, 87 757 –769 (2005). http://dx.doi.org/10.1016/j.solmat.2004.07.049 Google Scholar
© 2011 Society of Photo-Optical Instrumentation Engineers (SPIE) 1947-7988/2011/1(1)/019501/6/$25.00
Minlin Jiang, Yong Li, Rabin Dhakal, Prem S. Thapaliya, Michael A. Mastro, Joshua Caldwell, Fritz J. Kub, and Xingzhong Yan "Cu2ZnSnS4 polycrystalline thin films with large densely packed grains prepared by sol-gel method," Journal of Photonics for Energy 1(1), 019501 (1 January 2011). https://doi.org/10.1117/1.3628450
Published: 1 January 2011
Lens.org Logo
CITATIONS
Cited by 58 scholarly publications.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Thin films

Sol-gels

Copper

Annealing

Solar cells

Tin

Zinc

Back to Top