Advances in Condensed Matter Physics

Advances in Condensed Matter Physics / 2021 / Article

Research Article | Open Access

Volume 2021 |Article ID 7700676 |

Ali Hendaoui, "Substrate Temperature-Dependent Structural, Optical, and Electrical Properties of Thermochromic VO2(M) Nanostructured Films Grown by a One-Step Pulsed Laser Deposition Process on Smooth Quartz Substrates", Advances in Condensed Matter Physics, vol. 2021, Article ID 7700676, 8 pages, 2021.

Substrate Temperature-Dependent Structural, Optical, and Electrical Properties of Thermochromic VO2(M) Nanostructured Films Grown by a One-Step Pulsed Laser Deposition Process on Smooth Quartz Substrates

Academic Editor: Prasenjit Guptasarma
Received11 Jun 2021
Accepted27 Aug 2021
Published06 Sep 2021


Thermochromic M-phase vanadium dioxide VO2(M) films with different morphologies have been grown directly on smooth fused quartz substrates using low deposition rate pulsed laser deposition without posttreatment. When the substrate temperature was increased in the range 450°C–750°C, better (011) texturization of VO2(M) films was observed along with an enhancement of their crystallinity. Morphology evolved from small-grained and densely packed VO2(M) grains at 450°C to less packed micro/nanowires at 750°C. Mechanisms behind the crystallinity/morphology evolution were discussed and correlated with the effect of the temperature on the diffusion of the adatoms as well as on the V5+ valence states content in VO2(M) films. Resistivity measurements as a function of temperature revealed that the insulator-to-metal transition features of VO2(M) films (i.e., transition temperature (TIMT), resistivity variation (ΔR), hysteresis width (ΔH), and transition sharpness (ΔT)) are strongly dependent on the processing temperature. In terms of optical properties, it was found that the open (i.e., porous) structure of the films achieved at high temperature induced an improvement of their luminous transmittance. Simultaneously, the enhancement of the films crystallinity with the temperature resulted in better IR modulation ability. The present contribution provides a one-step process to control the morphology of VO2(M) films grown on smooth quartz substrates for applications as switches, memory devices, and smart windows.

1. Introduction

Thermochromic M-phase Vanadium dioxide VO2(M) undergoes an insulator-to-metal transition (IMT) that takes place around a temperature of TIMT ≈ 340K. Below TIMT, VO2(M) has a monoclinic phase characterized by a high resistivity (insulator). Above TIMT, VO2(M) displays a tetragonal phase with metallic characteristics. The IMT is reversible and takes place at ultrafast timescales and is characterized by a dramatic change in its resistivity as well as in its infrared optical properties from being highly transmissive to being highly reflective, while the optical properties in the visible range remain almost unchanged across TIMT [13]. This makes VO2(M) very promising for ultrafast electronic switching devices, memristors, and smart windows applications, especially since the critical temperature can be decreased to room temperature by donor-level doping [2]. Full exploitation of the IMT in VO2(M) requires a thorough control of its IMT features, such as TIMT, hysteresis width ΔH, and modulation capability of its electrical and/or optical properties depending on the targeted application. For example, a sensor would require a small hysteresis, sharp transition, and large modulation, while a memristor requires a large hysteresis. It is worth mentioning that the IMT characteristics in VO2(M) films depend on their crystallinity and grain morphology, in addition to the impurity/dopants content [4, 5].

Several reports in the literature describe studies on VO2(M) with controlled IMT properties for targeted applications [18]. Among them, pulsed laser deposition (PLD) holds a privileged position for the productions of pure VO2(M) thin films with controlled composition, crystallinity, and morphology [25]. It has also the potential for large-scale production, especially if the thin films’ synthesis is performed at low deposition rates [9]. The crystallinity and morphology of the VO2(M) films can be controlled via several parameters, including the substrate’s temperature during the deposition process. By controlling the substrate temperature at 700°C, in a recent report, Lafane et al. reported the synthesis of VO2(M) polycrystalline nanoplatelets on glass substrate by PLD using Vanadium Pentoxide V2O5 target under oxygen ambient [10]. However, Lafane et al. did not report information about the composition of the films. In addition, the functional properties of the grown nanoplatelets are not reported therein [10]. In summary, despite the importance of the substrate temperature for controlling the IMT characteristics of PLD-grown nanostructured VO2(M) films, the related studies remain relatively scarce. In addition, the influence of the substrate temperature on the vanadium valence content of the PLD-grown nanostructured VO2(M) films on smooth quartz substrates remains, to the best of our knowledge, unexplored.

Another important topic of interest related to the present study is related to the synthesis of VO2(M) micro/nanowires (MNWs). In fact, many approaches have been developed to achieve VO2(M) MNWs. In most of the cases, the proposed methods resulted in relatively low yield (i.e., surface density) for the micro/nanowires [11, 12]. As a remedial solution, roughening the substrate surface, patterning it, or using epitaxial growth were proposed [1114]. However, these approaches are either not suitable for optical applications (roughness and patterning), or not applicable for large-scale production (epitaxy). For example, optical applications such as smart windows require large transmittance of the samples in the visible range of the spectrum. In this sense, smooth surface substrates are needed because the presence of roughness or patterns on the substrates surface would negatively impact the optical transmittance. As for the epitaxy, it could be a limiting factor for large scale, that is, commercial production of thin films, since it requires the use of costly single crystalline substrates with atomic-level smoothness and specific lattice characteristics, such as single crystalline titanium dioxide or sapphire substrates for growing VO2(M), in order to ensure lattice matching between the substrate and the films.

In this paper, we will investigate the influence of the temperature on the composition, structure, and electrical and optical properties of VO2(M) films directly grown on smooth fused quartz substrates by a simple PLD approach at a low deposition rate without posttreatment. Smooth quartz substrates were chosen as they are convenient for resistivity measurements and suitable for optical applications.

We will demonstrate that a control of the substrate temperature of the PLD-grown VO2(M) films allows the control of their IMT features as revealed by resistivity measurement. On the other hand, we will demonstrate that, as the morphology changes from densely packed small grains to less packed micro/nanowires with increasing the temperature, an enhancement of luminous transmittance of the films is obtained. In addition, we will show that the improvement of VO2(M) crystallinity with the temperature results in an improvement of infrared (IR) transmittance modulation ability toward smart windows applications.

2. Materials and Methods

PLD was performed using KrF excimer pulsed laser (λ = 248 nm, fluence = 1.8−2) focused on Vanadium target (99.9% pure) under 5 mTorr of oxygen ambient. Such a low pressure was chosen as it is expected to be beneficial for producing elongated structures due to the enhanced mobility of the adatoms on the substrate. The total number of laser pulses on the target for each deposition experiment was set at 18000 pulses. Smooth fused quartz, used as the substrate, was kept at 7 cm away from the target and the substrate temperature was varied for the different experiments. The laser was pulsed at a frequency of 2 Hz. The choice of this value is based on preliminary tests on the influence of the laser pulsing frequency on the morphology of the grown films toward the synthesis of VO2(M) micro/nanowires. In fact, as shown in Figure S1 on the supplemental file, scanning electron microscope (SEM) images revealed that a pulsing frequency of 2 Hz is suitable for achieving elongated, rods-like structures for VO2(M) grains for films grown at the same substrate temperature.

X-ray photoelectron spectroscopy (XPS) measurements were made using a VG Escalab 220I-XL system with Al Kα (hν = 1486.6 eV) radiation. Etching with Argon was performed for 900-second prior measurements to surface contamination and/or overoxidation. More details about the deconvolution analysis of the binding energy of the V2p3/2 core level peak to determine the vanadium valence state content of the samples are given in the supplemental file (cf. Figure S2 in the supplemental file).

The crystalline structure of the samples was analyzed by X-ray diffraction (PANalytical's X'Pert, Cu Kα radiation). Their morphology was studied using scanning electron microscopy (JEOL JSM-6300F). The resistivity of the films was measured in the range 25°C–100°C using four-point probe. Optical transmittance was analyzed in the range of 250–2500 nm using a spectrophotometer (Agilent, Cary 5000) at normal incidence.

The integral luminous transmittance (390–830 nm) and IR transmittance (830–2500 nm) were calculated using the following equation:where is the IR irradiance spectrum for air mass 1.5 for a 37° tilted surface [15] and is the CIE (2008) physiologically relevant luminous efficiency function for photopic vision [16].

The modulation is defined as , where and are, respectively, the integral IR transmittance at room temperature and at 90°C.

3. Results and Discussion

3.1. Composition Analysis

Figure 1 shows the evolution of the V5+, V4+, and V2+ valence states content with the substrate temperature extracted from XPS measurements. As can be seen in Figure 1, V4+ is the dominant valence in the sample, which corresponds to the state related to VO2. V4+ content decreases in favor of an increase in the V5+ content with increasing the temperature. Therefore, higher oxidation of the films is obtained with increasing the temperature. On the other hand, the content in V2+ remains relatively constant as a function of the temperature as it originates from the creation of oxygen vacancies during the Argon etching process rather than the films PLD synthesis process itself.

3.2. Microstructure and Morphology Analysis

Figure 2 shows the XRD patterns of the VO2(M) films. All the peaks could be identified using Joint Committee on Powder Diffraction Standards (JCPDS) Card No. 44-0252 and were attributed to VO2 (M) monoclinic phase. (011) preferred orientation of the films was identified for the peak present at∼28° indicating texturization of VO2(M) along the (011) plane as it is the energetically favored one [17, 18]. The preferential crystal growth along the (011) plane is enhanced as the substrate temperature increases from 450°C to 750°C as shown by the increase in the (011) peak intensity. The inset in Figure 1 shows that the full width at half maximum (FWHM) of peak (011) decreases with increasing the substrate temperature, indicating an improvement of the crystallinity for the VO2 (M).

Figure 3 presents the top-view SEM images of VO2(M) films obtained at different substrate temperatures. At 450°C, the VO2 (M) film shows a small-grained, densely packed structure due to the relatively low diffusion of adatoms alongside the high nucleation rate that characterizes the PLD process. At 550°C, the structure displays the coexistence of grains and platelets. The sample synthesized at 650°C shows the formation of micro/nanorods with well-defined facets and a low aspect ratio.

The evolution of the microstructure and morphology of VO2(M) films with varying the processing temperature from 450°C to 650°C can be explained by the increase of the diffusion due to a concurrent effect of the temperature and the V5+ content. In fact, increasing the temperature not only improves the diffusion of the ad-atoms but also increases V5+ content in the films. Since V5+ state suggests the existence of V2O5, bulk diffusion is favored due to the low melting temperature of V2O5 (∼680°C) in accordance with the structural zone model for film growth described by Movchan-Demchishin [19]. More pronounced (011) texturization and better crystallinity of the VO2(M) films are obtained as the consequence of enhanced diffusion of the adatoms to grow the planes with the lowest energy [17, 18]. At the same time, the improvement of the diffusion helps in minimizing surface and interface energies by allowing the growth of large grains at the expense of smaller grains.

At 750°C, the structure of VO2(M) changes significantly with the formation of micro/nanowires with a high aspect ratio. This temperature is above the melting point of V2O5 (∼680°C), which can exist as an intermediate liquid phase during the PLD growth of VO2(M) structures. The liquid V2O5 enhances the formation of micro/nanowires through the wetting assisted growth mechanism, as described by Strelcov et al. [18]. At the same time, the high nucleation rate for the PLD process is beneficial for increasing the surface density (i.e., the yield) of the micro/nanowires on smooth fused quartz substrates, while the high mobility of the PLD adatoms is expected to increase the aspect ratio of the micro/nanowires for a temperature lower than those reported for thermal evaporation-based techniques [20].

3.3. Electrical Characterization

The resistivity measurement as a function of the temperature of the VO2 samples deposited at T = 450°C, 550°C, and 650°C is shown in Figure 4. The resistivity of the film deposited at 750°C could not be measured as the related values were beyond the upper limit of the four-point probe setup. The increase of the resistivity of the films can be explained by two main reasons: first, high V5+ content at high temperature is correlated to the existence of excessive oxygen atoms that will induce holes (i.e., acceptor) doping in the VO2 films [21]. Second, as the temperature increases, the films become less dense (cf. SEM images in Figure 3), which will further contribute to the increase of their overall resistivity.

The IMT features were obtained from the resistivity curves as follows: the resistivity variation, ΔR, is defined as ΔR = log10(R25°C/R100°C), where R25°C and R100°C are the resistivity values at 25°C and 100°C, respectively. The first derivative of the resistivity versus temperature was fitted with a Gaussian function (cf. Figure 5). The insulator-to-metal transition temperature (TIMT) is obtained from the position of the minimum of the Gaussian fit of the first derivative of the curve resistivity = f(T) for the heating segment, while the hysteresis width (ΔH) is calculated as the difference between the minimum of the Gaussian fit of the first derivative for the heating segment (insulator-to-metal transition) and that for the cooling (metal-to-insulator transition) segment. Finally, the transition sharpness (ΔT) corresponds to the FWHM of the Gaussian fit curves. The corresponding results are summarized in Table 1.

Substrate temperature (°C)ΔR (orders of magnitude)TIMT (°C)ΔH (°C)ΔT (°C)


TIMT is observed to increase with increasing the substrate temperature (cf. Table 1). This can be explained by the acceptor-level doping of the films due to the increase in the V5+ valence content that tends to shift TIMT to higher values. The largest ΔR was achieved for the sample deposited at 450°C (3.18 orders). ΔR decreases with increasing the substrate temperature from 450°C to 650°C (cf. Table 1). This result is correlated to the V4+ content, so that large V4+ content corresponds to a larger ΔR. In parallel, the hysteresis loop ΔH increases for samples processed at higher temperature. This can be attributed to the increase of grain size as explained by Suh et al. [22]. Finally, the transition sharpness (ΔT) is known to depend on the type of defects and their concentration in the films as well as on the mechanical stress in the grains of different sizes [4, 2227]. At low substrate temperature, VO2(M) grains are of a relatively small size and display a low discrepancy in the size (cf. Figure 3(a)). In this case, ΔT is low indicating a sharp transition as a result of a low density of bulk defects [4, 23]. In addition, a symmetric hysteresis loop is observed. For VO2(M) films processed at high temperatures, the grain size increases along with the exacerbation of the discrepancy in the grain size (Figures 3(b) and 3(c)). As a result, ΔT increases and an asymmetric hysteresis loop is observed due to the more pronounced difference in the values of ΔT for the heating and cooling segments of the resistivity curves of the same sample.

3.4. Optical Properties of the VO2(M) Films toward Smart Windows Application

Several approaches were reported to improve the properties of VO2(M) for smart windows applications, such as doping, multilayer films, core-shell nanostructures, and patterning [28]. The main target is to improve the luminous transmittance along with achieving good IR transmittance modulation across TIMT. Despite the achieved promising results, the proposed approaches involve complicated synthesis and/or fabrication procedures that may severely limit practical application.

The spectral transmittance measured at room temperature presented in Figure 6(a) shows an enhancement when the substrate temperature of VO2(M) films increases. VO2(M) layer displays a more open structure when the substrate temperature increases (cf. Figure 3). The medium made of VO2(M) and pores will have a lower refractive index, which results in an increase in the transmittance with the porosity [29]. As a result, the integral luminous transmittance at room temperature increases from 38.4% for VO2(M) film deposited at 450°C to 44.6% for the micro/nanowire VO2(M) sample deposited at 750°C (cf. Table 2). This represents a relative increase in by 16.1%. The spectral transmittance measured at 90°C is presented in Figure 6(b). Similarly to the trend observed at room temperature, the integral luminous transmittance at 90°C increases from 37.2% for VO2(M) film deposited at 450°C to 43.0% for the micro/nanowire VO2(M) sample deposited at 750°C (cf. Table 2). This represents a relative increase in by 15.6%. It is important to highlight the fact that values are very similar at both room temperature (RT) and 90°C, which means that the visible luminosity remains very stable across the IMT critical temperature. This factor might be very convenient for smart windows applications since the objective is to have a stable visible luminosity while ensuring a good modulation of the transmittance in the IR.

Substrate temperature (°C) (%) (%) (%)


The IR transmittance modulation is observed to increase from 12.7% for VO2(M) film deposited at 450°C to 18.9% for the micro/nanowire VO2(M) sample deposited at 750°C (cf. Table 2). By correlating these results to the decrease in the FWHM (cf. inset in Figure 2), the improvement in the modulation properties can be explained by the improvement in the crystallinity of VO2(M) with increasing the temperature [30].

4. Conclusion

VO2(M) films with different morphologies were directly grown on smooth fused quartz substrates by a simple PLD approach at a low deposition rate without posttreatment. It was found that the increase in the substrate’s temperature not only results in an enhancement of the adatoms diffusion, but also increases the V5+ state content, resulting in a further improvement of bulk diffusion due to the low melting point of vanadium oxides containing V5+ valence state. As a result, XRD revealed better (011) texturization and improved crystallinity with increasing the temperature from 450°C to 750°C. In addition, the morphology the VO2(M) grains evolved from small-grained, closely packed structure at 450°C, to less packed micro/nanowires structure at 750°C. Resistivity variation as a function of temperature revealed that VO2(M) films obtained at low substrate temperature display low insulator-to-metal transition temperature (TIMT), large resistivity variation (ΔR), narrow hysteresis width (ΔH), sharp transition, and symmetric hysteresis loop. Increasing substrate temperature resulted in VO2 films with high TIMT, low ΔR, broad ΔH, smooth transition, and asymmetric hysteresis loop. These results were correlated to the composition/microstructure/morphology of the samples. In summary, these results are expected to help in tailoring the resistivity transition toward specific applications of the films such as ultrafast electronic switching devices and memristors.

In terms of optical properties of the VO2(M) samples, it was found that an increase in the processing temperature from 450°C to 750°C resulted in an improvement of their luminous transmittance because of the increase in the porosity of the films. On the other hand, the improvement of the crystallinity of VO2(M) grains results in an enhancement of the IMT modulation of the transmittance. In summary, the proposed approach allowed achieving a VO2(M) film in the form of micro/nanowires with  = 44.6%,  = 43.0%, and  = 18.9%. This combination of properties is promising for smart windows applications. We anticipate that further improvement could be possible through the optimization of micro/nanowires yield and size distribution. Also, it would be interesting to investigate the effect of dopants on VO2(M) micro/nanowires to have a synergetic approach for further enhancement of both luminous transmittance and IR modulation ability.

Data Availability

Data are available on request from the author.

Conflicts of Interest

The author declares no that there are conflicts of interest.


This work was supported by the Alfaisal University Office of Research and Graduate Studies (IRG project 21417). The author is grateful for the continuous support.

Supplementary Materials

Figure S1: SEM images of the PLD VO2(M) films grown at 650°C and different laser pulsing frequencies: (a) 20 Hz, (b) 14 Hz, (c) 8 Hz, and (d) 2 Hz. Figure S2: XPS spectra of the V2p3/2 peak deconvoluted into V5+, V4+, and V2+, for the samples processed at different substrate temperatures: (a) 450°C, (b) 550°C, (c) 650°C, and (d) 750°C. (Supplementary Materials)


  1. F. J. Morin, “Oxides which show a metal-to-insulator transition at the neel temperature,” Physical Review Letters, vol. 3, no. 1, pp. 34–36, 1959. View at: Publisher Site | Google Scholar
  2. A. Hendaoui, N. Émond, S. Dorval, M. Chaker, and E. Haddad, “VO2-based smart coatings with improved emittance-switching properties for an energy-efficient near room-temperature thermal control of spacecrafts,” Solar Energy Materials and Solar Cells, vol. 117, pp. 494–498, 2013. View at: Publisher Site | Google Scholar
  3. V. R. Morrison, R. P. Chatelain, K. L. Tiwari et al., “A photoinduced metal-like phase of monoclinic VO2 revealed by ultrafast electron diffraction,” Science, vol. 346, no. 6208, pp. 445–448, 2014. View at: Publisher Site | Google Scholar
  4. J. Narayan and V. M. Bhosle, “Phase transition and critical issues in structure-property correlations of vanadium oxide,” Journal of Applied Physics, vol. 100, Article ID 103254, 2006. View at: Publisher Site | Google Scholar
  5. N. Émond, A. Hendaoui, A. Ibrahim, I. Al-Naib, T. Ozaki, and M. Chaker, “Transmission of reactive pulsed laser deposited VO2 films in the THz domain,” Applied Surface Science, vol. 379, pp. 377–383, 2016. View at: Publisher Site | Google Scholar
  6. D. P. Partlow, S. R. Gurkovich, K. C. Radford, and L. J. Denes, “Switchable vanadium oxide films by a sol‐gel process,” Journal of Applied Physics, vol. 70, no. 1, pp. 443–452, 1991. View at: Publisher Site | Google Scholar
  7. M. B. Sahanna, M. S. Dharmaprakash, and S. A. Shivashankar, Mass Spectrometry Basics, vol. 12, 2002. View at: Publisher Site
  8. S. Mathur, T. Ruegamer, N. Donia, and H. Shen, “Functional metal oxide coatings by molecule-based thermal and plasma chemical vapor deposition techniques,” Journal of Nanoscience and Nanotechnology, vol. 8, no. 5, pp. 2597–2603, 2008. View at: Publisher Site | Google Scholar
  9. A. S. Kuzanyan and A. A. Kuzanyan, Pulsed Laser Deposition of Large‐Area Thin Films and Coatings, IntechOpen, London, UK, 2016.
  10. S. Lafane, S. Abdelli-Messaci, M. Kechouane et al., “Direct growth of VO2 nanoplatelets on glass and silicon by pulsed laser deposition through substrate temperature control,” Thin Solid Films, vol. 632, pp. 119–127, 2017. View at: Publisher Site | Google Scholar
  11. S. Löffler, E. Auer, M. Weil, A. Lugstein, and E. Bertagnolli, “Impact of growth temperature on the crystal habits, forms and structures of VO2 nanocrystals,” Applied Physics A, vol. 102, no. 1, pp. 201–204, 2011. View at: Publisher Site | Google Scholar
  12. I. S. Kim and L. J. Lauhon, “Increased yield and uniformity of vanadium dioxide nanobeam growth via two-step physical vapor transport process,” Crystal Growth & Design, vol. 12, no. 3, pp. 1383–1387, 2012. View at: Publisher Site | Google Scholar
  13. C. Cheng, K. Liu, B. Xiang, J. Suh, and J. Wu, “Ultra-long, free-standing, single-crystalline vanadium dioxide micro/nanowires grown by simple thermal evaporation,” Applied Physics Letters, vol. 100, no. 10, Article ID 103111, 2012. View at: Publisher Site | Google Scholar
  14. C. Cheng, H. Guo, A. Amini et al., “Self-assembly and horizontal orientation growth of VO2 nanowires,” Scientific Reports, vol. 4, no. 1, p. 5456, 2014. View at: Publisher Site | Google Scholar
  15. “ASTM G173-03 standard tables of reference solar spectral irradiances: direct normal and hemispherical on a 37 degree tilted surface,” 2020, View at: Google Scholar
  16. The Centre for International Economics, “Physiologically-relevant luminous efficiency function for photopic vision,” 2008, View at: Google Scholar
  17. K. Appavoo, D. Y. Lei, Y. Sonnefraud et al., “Role of defects in the phase transition of VO2 nanoparticles probed by plasmon resonance spectroscopy,” Nano Letters, vol. 12, no. 2, pp. 780–786, 2012. View at: Publisher Site | Google Scholar
  18. E. Strelcov, A. V. Davydov, U. Lanke, C. Watts, and A. Kolmakov, “In situ monitoring of the growth, intermediate phase transformations and templating of single crystal VO2 nanowires and nanoplatelets,” ACS Nano, vol. 5, no. 4, pp. 3373–3384, 2011. View at: Publisher Site | Google Scholar
  19. J. A. Thornton, “High rate thick film growth,” Annual Review of Materials Science, vol. 7, no. 1, pp. 239–260, 1977. View at: Publisher Site | Google Scholar
  20. R. Eason, Pulsed Laser Deposition of Thin Films Applications-Led Growth of Functional Materials, Wiley-Interscience, Hoboken, NJ, USA, 2007.
  21. Y. Zhao, C. Chen, X. Pan et al., “Tuning the properties of VO2 thin films through growth temperature for infrared and terahertz modulation applications,” Journal of Applied Physics, vol. 114, no. 11, Article ID 113509, 2013. View at: Publisher Site | Google Scholar
  22. J. Y. Suh, R. Lopez, L. C. Feldman, and R. F. Haglund Jr., “Semiconductor to metal phase transition in the nucleation and growth of VO2 nanoparticles and thin films,” Journal of Applied Physics, vol. 96, no. 2, pp. 1209–1213, 2004. View at: Publisher Site | Google Scholar
  23. P. Jin, K. Yoshimura, and S. Tanemura, “Dependence of microstructure and thermochromism on substrate temperature for sputter-deposited VO2 epitaxial films,” Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films, vol. 15, no. 3, pp. 1113–1117, 1997. View at: Publisher Site | Google Scholar
  24. R. Lopez, L. C. Feldman, and R. F. Haglund Jr., “Size-dependent optical properties ofVO2 nanoparticle arrays,” Physical Review Letters, vol. 93, no. 17, Article ID 177403, 2004. View at: Publisher Site | Google Scholar
  25. S. Lysenko, V. Vikhnin, A. Rua, F. Fernandez, and H. Liu, “Critical behavior and size effects in light-induced transition of nanostructured VO2 films,” Physical Review B: Condensed Matter, vol. 82, Article ID 205425, 2010. View at: Google Scholar
  26. R. Lopez, T. E. Haynes, L. A. Boatner, L. C. Feldman, and R. F. Haglund Jr., “Size effects in the structural phase transition ofVO2 nanoparticles,” Physical Review B, vol. 65, no. 22, Article ID 224113, 2002. View at: Publisher Site | Google Scholar
  27. W. Fan, J. Cao, J. Seidel et al., “Large kinetic asymmetry in the metal-insulator transition nucleated at localized and extended defects,” Physical Review B, vol. 83, no. 23, Article ID 235102, 2011. View at: Publisher Site | Google Scholar
  28. Y. Cui, Y. Ke, C. Liu et al., “Thermochromic VO2 for energy-efficient smart windows,” Joule, vol. 2, no. 9, pp. 1707–1746, 2018. View at: Publisher Site | Google Scholar
  29. S. Long, X. Cao, Y. Wang et al., “Karst landform-like VO2 single layer solution: controllable morphology and excellent optical performance for smart glazing applications,” Solar Energy Materials and Solar Cells, vol. 209, p. 110449, 2020. View at: Publisher Site | Google Scholar
  30. C. Kang, C. Zhang, Y. Yao et al., “Enhanced thermochromic properties of vanadium dioxide (VO2)/glass heterostructure by inserting a Zr-based thin film metallic glasses (Cu50Zr50) buffer layer,” Applied Sciences, vol. 8, no. 10, p. 1751, 2018. View at: Publisher Site | Google Scholar

Copyright © 2021 Ali Hendaoui. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.