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Research Paper

Applied Science and Convergence Technology 2021; 30(5): 152-155

Published online September 30, 2021

https://doi.org/10.5757/ASCT.2021.30.5.152

Copyright © The Korean Vacuum Society.

Effect of Reaction Time on Optical Properties of CsPbBr3 Perovskite Nanocrystals

Sung Hun Kima , Yong-Ryun Job , Yong Bin Kima,b , Ju Seok Kima , Sang-Youp Yimb , and Hong Seok Leea,*

aDepartment of Physics, Research Institute of Physics and Chemistry, Jeonbuk National University, Jeonju 54896, Republic of Korea
bAdvanced Photonics Research Institute, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea

Correspondence to:E-mail: hslee1@jbnu.ac.kr

Received: July 8, 2021; Revised: August 1, 2021; Accepted: August 4, 2021

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

We have studied the optical and structural properties of CsPbBr3 perovskite nanocrystals (NCs) fabricated with various reaction times. The temporal evolution of the ensemble optical properties, such as absorption and fluorescence (FL) spectra and photoluminescence quantum yield (PLQY), was recorded under a set reaction temperature (170 °C) and various amounts of time (5 s – 60 min). The FL intensity of the CsPbBr3 NCs gradually decreased with increasing reaction time, and the observed PLQY of the CsPbBr3 NCs ranged from less than 20% up to 35% because of the enlarged crystal size and the induced charge trap states. The FL peaks of as-obtained CsPbBr3 NCs were tuned in the range of 516.8 to 526.8 nm with increasing reaction time as a result of the ripening phenomenon. Transmission electron microscopy and selected area electron diffraction analysis were performed to analyze the structural properties. The results revealed that the average edge length of CsPbBr3 NCs with a reaction time of 5 s was 13.4 nm and confirmed that the cubic crystal structure was well ordered.

Keywords: Perovskite nanocrystals, CsPbBr3, Reaction time, Optical properties, Photoluminescence quantum yield

All-inorganic cesium lead halide perovskite nanocrystals (NCs) have attracted significant attention because they demonstrate higher tolerance compared to organic-inorganic perovskites such as CH3NH3PbX3 NCs in applications such as light-emitting diodes and solar cells [1, 2]. CH3NH3PbX3 perovskites are also strongly associated with autodegradation because of their intrinsic instabilities [3]. So it is necessary to realize an efficient strategy for solving these problems. The thermal durability of organic-inorganic perovskites is regarded as one of the most critical issues for solar cell performance [4]. Perovskite materials are vulnerable to damage during thermal annealing, and heat dissipation is known to have an influence on perovskites, which results in thermal-induced mechanical stress and structural evolution within the NCs [5]. In organic-inorganic hybrid perovskites, the occurrence of a structural phase transition is correlated with its own characteristics and the contents of ambient air, temperature, and pressure, which have an effect on the durability of perovskite solar cells [6]. Replacement of the methylammonium (MA) cation with the less active cation of Cs can allow CsPbBr3 NCs to exhibit superior thermal stability, chemical durability, and striking optical properties [7, 8]. The purpose of substituting MA cation is to form a more stable cubic phase, along with the appropriate modulation of the conduction band of the perovskite, which is the key feature to achieve stability [9]. Therefore, tailoring the optical properties of CsPbBr3 NCs to make them more suitable for application is a promising approach [10]. CsPbBr3 NCs can be fabricated employing a method in which oleylamine (OAm) and oleic acid (OA) are used as capping agents. The carboxylate and amine functional groups of OA and OAm are attached to the surface of the NCs during the reaction, resulting in the stability of the NCs. These long-chain hydrocarbon ligands promote the dispersion of CsPbBr3 NCs in various organic media [11]. In particular, to fulfill the requirements for optoelectronic devices, the optical properties, growth stage, morphology, and structure of CsPbBr3 NCs should be regulated during reproducible preparation, and various challenges in the synthetic strategy should be addressed [12].

To obtain more insight into this process, we here report the optical properties of CsPbBr3 perovskite NCs fabricated with various reaction times. The UV-vis absorption and fluorescence (FL) measurements were conducted with a focus on the deterioration of the optical properties of the CsPbBr3 NCs. Significant changes were also observed in the photoluminescence quantum yield (PLQY) of the CsPbBr3 NCs with various reaction times. In addition, the single-crystalline cubic-phase CsPbBr3 NCs and their size distributions were determined via field-emission transmission electron microscopy (FETEM).

For the preparation of Csoleate, Cs2CO3(0.391 g, 1.2 mmol), OA (1.27 mL, 4 mmol), and 1-octadecene (18.73 mL) were loaded into a 100 mL three-neck flask and vacuumed for 1 h at 120 °C. Then, the mixture was reacted at 160 °C under flowing N2 gas until the precur-sor solution was completely dissolved. Because Cs-oleate precipitates out of 1-octadecene at room temperature, it needs to be preheated to 100 °C before use. Next, for the synthesis of CsPbBr3 NCs with vari-ous reaction times, PbBr2 (0.149 g, 4 mmol) and 1-octadecene (18.73 mL) were placed in a 100 mL three-neck flask and vacuumed for 1 h at 120 °C, after which OA (1 mL) and OAm (3 mL) were injected at 120 °C. After PbBr2 was completely solubilized, the mixture was heated up to 170 °C, and 2 mL of the Cs-oleate stock solution was injected swiftly into the reaction system. Subsequently, the sample was ob-tained after a set reaction time (5 s, 1, 5, 10, 20, 30, and 60 min). Then, the reaction mixture was cooled down with an ice-water bath. The resulting mixture was precipitated with tert-butanol by centrifugation at 7,000 rpm for 10 min. After centrifugation, the supernatant was eliminated, and the resulting precipitate was obtained. The resulting precipitate was re-dispersed in toluene for UV-vis and TEM measure-ments. UV-vis absorption and FL measurements of the CsPbBr3 NCs were performed using a FLAME-S spectrophotometer (Ocean Optics Inc., Largo, FL, USA) at room temperature. The crystalline structure, morphology and size distributions of the CsPbBr3 NCs were investi-gated by using a FETEM (Tecnai G2, F30 S-Twin, 300 keV, Thermo Fisher Scientific, Waltham, MA, USA).

The FL and absorption spectra of CsPbBr3 NCs with various reac-tion times are shown in Fig. 1. The crystallite growth of CsPbBr3 NCs in solution primarily depends on the LaMer mechanism [13]. The growth stage of the CsPbBr3 NCs can be divided into three distinct phases, i.e., the nucleation, growth, and regrowth processes. The hot-injection in wet chemical route for colloidal synthesis of the CsPbBr3 NCs has benefits with respect to controlling particle size and size dis-tribution [14]. At 5 s of reaction time, the CsPbBr3 NCs showed a sharp absorption and a narrow emission peak. The full-width at half-maximum for the CsPbBr3 NCs was 20.2, 18.6, 19.3, 18.8, 18.7, 19.9, and 20.3 nm for reaction times of 5 s, 1, 5, 10, 20, 30, and 60 min, respectively. As the reaction time increased, the FL peaks gradually decreased because of the loss of the quantum size effect induced by abnormal growth, as shown in Fig. 1(a) [15]. When the reaction time increased up to 5 min, the absorption peaks of the CsPbBr3 NCs re-mained unchanged, as depicted in Fig. 1(b). After 5 min of reaction time, the absorption peaks for the CsPbBr3 NCs became broader. The intensity of the absorption spectra gradually decreased with increas-ing reaction time, suggesting a decrease in the light absorption capac-ity [16].

Figure 1. (a) Fluorescence and (b) absorption spectra of CsPbBr3 nanocrystals with various reaction times.

The variations of the FL peak position and intensity of the CsPbBr3 NCs as a function of reaction time are displayed in Fig. 2. The FL peaks of as-obtained CsPbBr3 perovskite NCs produced at reaction times of 5 s, 1, 5 , 10, 20, 30, and 60 min are located at 516.8, 518.2, 517.5, 517.9, 517.9, 519.3, and 526.8 nm, respectively. The redshift in the FL peaks of the CsPbBr3 NCs with increasing reaction time is due to the ripening of CsPbBr3 NCs [12,17]. The FL intensities decreased steadily, and the FL peaks nearly disappeared with increasing reaction time, as shown in Fig. 2, which can be attributed to the increased size of the CsPbBr3 crystal. The CsPbBr3 NCs were diluted with toluene solutions to give the same band edge optical density (0.05 at the respective band edge absorption peaks). The FL intensity of the CsPbBr3 NC sample with a reaction time of 60 min decreased by nearly 20 times compared with that of the CsPbBr3 NC sample with a reaction time of 5 s. These results are related to the induced charge trap states resulting from the surface decomposition reaction or the elimination of surface ligands [3].

Figure 2. Fluorescence peak position and intensity of CsPbBr3 nanocrystals as a function of reaction time.

Figure 3(a) shows the photoluminescence quantum yields (PLQYs) of the CsPbBr3 NCs synthesized at a set reaction temperature (170 °C) and varying reaction times (5 s – 60 min). The relative PLQY of the CsPbBr3 NCs were obtained by comparing the integrated emis-sion of the CsPbBr3 NC samples with a standard fluorescence dye (Coumarin 500 in ethanol, QY = 47%) [18]. The absorbance of the CsPbBr3 NC samples was kept at less than 0.1 at 390 nm to prevent re-absorption [19]. The CsPbBr3 NCs exhibited relative PLQYs (20–35%). The highest PLQY (35%) was attained for CsPbBr3 NCs pre-pared at a reaction time of 5 s, and the overall PLQY decreased as the reaction time increased because of the change in size and mor-phology of CsPbBr3 NCs [20]. Figures 3(b) and 3(c) show the digital photographs of the as-obtained CsPbBr3 NCs prepared at various re-action times under white light and single 365 nm UV light source. PL quenching of the CsPbBr3 NCs can be also observed with the naked eye under a UV light, as seen in Fig. 3(b). As the reaction time in-creased, the solution containing CsPbBr3 NCs, with a yellow precip-itate and colorless transparent supernatant, turned dark and became turbid. The initial light green color of CsPbBr3 NCs turned to yellow phases with increasing reaction time, suggesting extensive precipita-tion of the CsPbBr3 NCs prepared at high temperature as shown Fig. 3(c). The yellow phases are caused by large CsPbBr3 crystal growth, and this phenomenon revealed a broader size distribution [3, 16].

Figure 3. (a) Photoluminescence quantum yields of CsPbBr3 nanocrystals as a function of reaction time. The digital photographs of the as-obtained CsPbBr3 nanocrystals synthesized at various reaction time under (b) single 365 nm UV light and (c) white light.

Figures 4(a) and 4(b) represent the low-magnification bright-field TEM image and selected-area diffraction (SAED) pattern of CsPbBr3 NCs on the specific high temperature (≥130 °C) and reaction time (5 s). As shown in Fig. 4(a), almost all of the square-shaped CsPbBr3 NCs uniformly formed at 170 °C, which is well-matched with already reported morphological characteristics of conventional colloidal CsPbBr3 NCs [16,21]. The SAED ring pattern in Fig. 4(b) indicates that the lat-tice spacing of 0.41, 0.29, and 0.21 nm corresponds to the (110), (200), and (220) lattice planes, which agree well with the interplanar spacings of cubic-phase CsPbBr3, respectively [22]. The nanostructural characteristics of the CsPbBr3 NCs are also confirmed via the high-resolution TEM image depicted in Fig. 4(c) and fast Fourier transform pattern obtained from [001] beam direction (Z, zone axis). The lattice spacing of 0.41 and 0.58 nm corresponds to the (110) and (100) interplanar spacings of cubic-phase CsPbBr3, respectively [22, 23]. The number of CsPbBr3 NCs and size distributions is plotted with Gaussian distributions, as shown in Fig. 4(d), and the average size of the CsPbBr3 NCs is 13.4 nm. The histogram of the particle size distribution for the CsPbBr3 NCs was obtained by using ImageJ software [17, 24].

Figure 4. (a) Bright-field transmission electron microscopy image and (b) selected-area diffraction pattern of the CsPbBr3 nanocrystals (170 °C, 5 s). (c) High-resolution transmission electron microscopy image from the black dotted box in (a) and the inset is a fast Fourier transform pattern of corresponding image. (d) Histogram of the size distribution of the CsPbBr3 nanocrystals.

We investigated the influence of reaction time on the structural and optical properties of assynthesized CsPbBr3 perovskite NCs. The reaction conditions of CsPbBr3 NCs can significantly affect the structure and crystal form of the NCs. The redshift of the FL wavelength and resultant decrease in the total absorption intensity with increasing reaction time was attributed to large CsPbBr3 crystal growth by the ripening process. With increasing reaction time, the FL intensities and PLQYs gradually decreased because of the loss of quantum confinement and formation of charge trap states. TEM observations demonstrated that the CsPbBr3 NCs with an initial reaction time of 5 s were well-crystallized in a cubic lattice. Our observations provide clear evidence that the CsPbBr3 perovskite NCs are significantly affected by the reaction conditions, which can lead to significant changes in the particle morphology and associated optical properties. The results of this study suggest the importance of investigation of the optical properties in CsPbBr3 NCs with various synthetic factors affecting the reliability and durability of optoelectronic devices.

This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (NRF-2021R1A2C1003074).

  1. H. Wang., et al, Nat. Commun. 10, 665 (2019).
    Pubmed KoreaMed CrossRef
  2. H. Yuan, Y. Zhao, J. Duan, Y. Wang, X. Yang, and Q. Tang, J. Mater. Chem. A 6, 24324 (2018).
    CrossRef
  3. S. Huang, Z. Li, B. Wang, N. Zhu, C. Zhang, L. Kong, Q. Zhang, A. Shan, and L. Li, ACS Appl. Mater. Interfaces 9, 7249 (2017).
    Pubmed CrossRef
  4. P. Wang, N. Chai, C. Wang, J. Hua, F. Huang, Y. Peng, J. Zhong, Z. Ku, and Y.-b. Cheng, RSC Adv. 9, 11877 (2019).
    CrossRef
  5. J. Chen, D. Liu, M. J. Al-Marri, L. Nuuttila, H. Lehtivuori, and K. Zheng, Sci. China Mater. 59, 719 (2016).
    CrossRef
  6. G. Niu, X. Guo, and L. Wang, J. Mater. Chem. A 3, 8970 (2015).
    CrossRef
  7. R. G. Niemann, L. Gouda, J. Hu, S. Tirosh, R. Gottesman, P. J. Cameron, and A. Zaban, J. Mater. Chem. A 4, 17819 (2016).
    CrossRef
  8. E. Erol, O. Kıbrıslı, M. Ç. Ersundu, and A. E. Ersundu, Chem. Eng. J. 401, 126053 (2020).
    CrossRef
  9. Z. Wang, Z. Shi, T. Li, Y. Chen, and W. Huang, Angew. Chem. Int. Ed. 56, 1190 (2017).
    Pubmed CrossRef
  10. P. Song, B. Qiao, D. Song, Z. Liang, D. Gao, J. Cao, Z. Shen, Z. Xu, and S. Zhao, J. Alloys Compd. 767, 98 (2018).
    CrossRef
  11. J. Song, J. Li, X. Li, L. Xu, Y. Dong, and H. Zeng, Adv. Mater. 27, 7162 (2015).
    Pubmed CrossRef
  12. Y. Xu, S. Lou, C. Xia, T. Xuan, and H. Li, J. Lumin. 222, 117132 (2020).
    CrossRef
  13. V. K. LaMer and R. H. Dinegar, J. Am. Chem. Soc. 72, 4847 (1950).
    CrossRef
  14. X. Li, K. Zhang, J. Li, J. Chen, Y. Wu, K. Liu, J. Song, and H. Zeng, Adv. Mater. Interfaces 5, 1800010 (2018).
    CrossRef
  15. T. Kosugi, Y. Iso, and T. Isobe, Chem. Lett. 48, 349 (2019).
    CrossRef
  16. J. Lan, L. Luo, M. Wang, F. Li, X. Wu, and F. Wang, J. Lumin. 210, 464 (2019).
    CrossRef
  17. M. Koolyk, D. Amgar, S. Aharon, and L. Etgar, Nanoscale 8, 6403 (2016).
    Pubmed CrossRef
  18. S. H. Kim, K.-D. Park, and H. S. Lee, Energies 14, 275 (2021).
    CrossRef
  19. S. L. Hu, K. Y. Niu, J. Sun, J. Yang, N. Q. Zhao, and X. W. Du, J. Mater. Chem. 19, 484 (2009).
    CrossRef
  20. C. Chen, L. Zhang, T. Shi, G. Liao, and Z. Tang, Nanomaterials 9, 1751 (2019).
    Pubmed KoreaMed CrossRef
  21. X. Zhang, B. Xu, J. Zhang, Y. Gao, Y. Zheng, K. Wang, and X. W. Sun, Adv. Funct. Mater. 26, 4595 (2016).
    CrossRef
  22. M. Rodová, J. Brožek, K. Knížek, and K. Nitsch, J. Ther. Anal. Calorim. 71, 667 (2003).
    CrossRef
  23. L. Yang, B. Fu, X. Li, H. Chen, and L. Li, J. Mater. Chem. C 9, 1983 (2021).
    CrossRef
  24. S. H. Kim, M. T. Man, J. W. Lee, K.-D. Park, and H. S. Lee, Nano-materials 10, 1589 (2020).
    Pubmed KoreaMed CrossRef

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