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Infrared imaging systems are being updated towards greater performance as well as lighter and smaller devices. Developing infrared materials with special properties is a critical for enhancing the performance of optical systems as well as miniaturizing devices. Chalcogenide glass becomes a popular option for advanced IR materials due to its component-property tunability. Se—based glasses such as Ge33As12Se55, Ge10As40Se50, and As40Se60, which completely cover the mid- and long-wave infrared windows, are the most typical materials used in infrared equipment. However, these classical materials can no longer meet the requirements of high-performance imaging systems, and adding more elements such as Te, Ga, Sb, and Ag to enhance the performance is a reliable way to solve this problem. By analysing the structure and properties of the Ge20Se80–xTex glass system, the law of its structure and properties evolving with Te content is illustrated. The obtained typical results are shown below. With the increase of Te content, the glass transition temperature (Tg) increases and then decreases, which is caused by the network structure and the average bond energy; the density and refractive index increase in an approximately linear gradient; the Abbe number gradually increases, while the Vickers hardness hardly changes with Te content; the fracture toughness decreases with the Te content increasing. Aiming at the problem that the average coordination number is unable to evaluate the glass systems composed of two or more elements from the same main group, a theoretical bandgap-glass property evaluation system is successfully established. The functional relationships among parameters such as density, refractive index, Abbe number, and fracture toughness, and theoretical band gap are established for Ge20Se80–xTex glass system as shown in the summary figure, which can be used to rapidly evaluate the glass components and properties.
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Keywords:
- infrared materials /
- chalcogenide glasses /
- theoretical bandgap /
- glass property
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Google Scholar
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图 1 (a) Ge20Se80–xTex系列玻璃直接带隙对应的(αhν)2和hν之间的关系, 以及每种玻璃的光学带隙值; (b) 理论带隙、光学带隙与Te含量的变化关系
Figure 1. (a) The relationship between (αhν)2 and hν corresponding to the direct band gap of Ge20Se80–xTex series glasses, and the optical band gap value of each glass; (b) the relationship between the theoretical bandgap, the optical bandgap and the Te content.
图 2 (a) Ge20Se80–xTex系列玻璃归一化拉曼光谱; (b) Ge20Se50Te30玻璃拉曼光谱曲线拟合
Figure 2. (a) Normalised Raman spectra of Ge20Se80–xTex series glasses; (b) Raman spectral curve fitting of Ge20Se50Te30 glasses.
图 3 Ge20Se80–xTex系列玻璃的Tg随Te含量的变化
Figure 3. The relationship between the Tg of Ge20Se80–xTex series glass and the Te content.
图 4 Ge20Se80–xTex系列玻璃的密度(a)、折射率@10 μm (b)、以及8—12 μm窗口的阿贝数 (c)与Te含量的变化关系; Ge20Se80–xTex系列玻璃的密度(d)、折射率@10 μm(e)、以及8—12 μm窗口的阿贝数(f)与理论带隙$ E_{\text{g}}^{{\text{th}}} $的变化关系及其拟合曲线
Figure 4. Variation of density (a), refractive index @10 μm (b), and Abbe number (c) for the 8–12 μm window versus Te content for Ge20Se80–xTex series glasses; variation of density (d), refractive index @10 μm (e), and Abbe number (f) for the 8–12 μm window versus the theoretical bandgap $ E_{\text{g}}^{{\text{th}}} $and their fitting curves for the Ge20Se80–xTex series glasses.
图 5 Ge20Se80–xTex系列玻璃的维氏硬度(a)、断裂韧性(b)与Te含量的变化关系; Ge20Se80–xTex系列玻璃的维氏硬度(d)、断裂韧性(e)与理论带隙$ E_{\text{g}}^{{\text{th}}} $的变化关系及其拟合曲线
Figure 5. Variation of Vickers hardness (a) and fracture toughness (b) versus Te content for the Ge20Se80–xTex series of glasses; variation of Vickers hardness (d) and fracture toughness (e) versus the theoretical bandgap $ E_{\text{g}}^{{\text{th}}} $, and their fitted curves for the Ge20Se80–xTex series of glasses.
表 1 Ge, Se, Te元素的基本特性参数
Table 1. The basic characteristic parameters of Ge, Se, and Te elements.
元素 配位数 密度/(g·cm–3) 摩尔质量/(g·mol–1) 摩尔体积/(cm3·mol–1) 电负性Pauling scale 带隙/eV 键能/(kcal·mol–1) Ge 4 5.33 72.63 13.63 2.01 0.67 37.78 Se 2 4.81 78.97 16.42 2.55 1.95 44.04 Te 2 6.22 127.6 20.50 2.10 0.33 33.00 
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表 2 Ge20Se80–xTex的玻璃可能出现的共价键及其键能
Table 2. Possible bond types and bond energies for Ge20Se80–xTex glass.
成键类型 Ge—Se Se—Te Se—Se Ge—Te Te—Te 键能/(kcal·mol–1) 49.54 44.20 44.04 35.55 33.00
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表 3 Ge20Se80–xTex系列玻璃可能出现的振动模式及其频率位置
Table 3. Possible vibration modes and frequency positions of Ge20Se80–xTex series glasses.
Wavenumber/cm–1 Vibrational mode 145 ν (Te)—Te–Te—(Te) 151 νas (Ge)—Te—Te—Te—(Ge) 154 νs (Ge)—Te—Te—Te—(Ge) 157 ν (Ge)—Te—Te—(Te) 164 ν (Ge)—Te—Te—(Ge) 145 ν Ge—Se1/2Te3/2 160 ν Ge—Se2/2Te2/2 170 ν Ge—Se3/2Te1/2 194 νs Corner-Sharing Ge—Se4/2 211 νs Edge-sharing Ge—Se4/2 299 νas Ge—Se4/2 208 νas (Ge)—Te—Se—Te—(Ge) 210 ν (Se)-Se—Te—(Ge) 211 νs (Ge)—Te—Se—Te—(Ge) 212 νas (Ge)-Se—Te—Se—(Ge) 219 νs (Te)—Te—Se—(Ge) 222 νs (Ge)-Se—Te—Se—(Ge) 245 ν -(Se—Se)n- long chain 252 νas Se—Se—Se 263 ν (Se)-Se—Se—(Ge) 270 ν Se—Se
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[1] Adam J L, Zhang X H 2014 Chalcogenide Glasses (Sawston Cambridge: Woodhead Publishing) pxvii
[2] Maurugeon S, Boussard-Pledel C, Troles J, Faber A J, Lucas P, Zhang X H, Lucas J, Bureau B 2010 J. Lightwave Technol. 28 3358
[3] Calvez L, Ma H L, Lucas J, Zhang X H 2007 Adv. Mater. 19 129
Google Scholar
[4] Mi H T, Yang A P, Huang Z X, Tian K Z, Li Y B, Ma C, Liu Z J, Shen X, Yang Z Y 2023 Acta Phys. Sin. 72 047101 [米浩婷, 杨安平, 黄梓轩, 田康振, 李跃兵, 马成, 刘自军, 沈祥, 杨志勇 2023 物理学报 72 047101]
Google Scholar
Mi H T, Yang A P, Huang Z X, Tian K Z, Li Y B, Ma C, Liu Z J, Shen X, Yang Z Y 2023 Acta Phys. Sin. 72 047101
Google Scholar
[5] Wang Y W, Qi S S, Yang Z Y, Wang R P, Yang A P, Lucas P 2017 J. Non-Cryst. Solids 459 88
Google Scholar
[6] Carlie N A 2015 Int. J. Appl. Glass Sci. 6 364
Google Scholar
[7] Lonergan J, Lonergan C, McCloy J, Richardson K A 2019 J. Non-Cryst. Solids 510 192
Google Scholar
[8] Yang G, Gueguen Y, Sangleboeuf J-C, Rouxel T, Boussard-Plédel C, Troles J, Lucas P, Bureau B 2013 J. Non-Cryst. Solids 377 54
Google Scholar
[9] Wang T, Wei W H, Shen X, Wang R P, Davies B L, Jackson I 2013 J. Phys. D: Appl. Phys. 46 165302
Google Scholar
[10] Wang R P, Wang T, Choi D Y, Madden S, Luther-Davies B 2011 AIP Conf. Proc. 1393 34
[11] Xu S W, Liang T, Zhu X Y 2023 Chalcogenide Lett. 20 55
Google Scholar
[12] Xu S W, Wang X S, Shen X 2024 Acta Phys. Sin. 73 057102 [许思维, 王训四, 沈祥 2024 物理学报 73 057102]
Google Scholar
Xu S W, Wang X S, Shen X 2024 Acta Phys. Sin. 73 057102
Google Scholar
[13] Phillips J C 1979 J. Non-Cryst. Solids 34 153
Google Scholar
[14] Xia F, Baccaro S, Wang H, Hua W, Zeng H D, Zhang X H, Chen G R 2008 J. Non-Cryst. Solids 354 1365
Google Scholar
[15] Opletal G, Wang R P, Russo S P 2013 Phys. Chem. Chem. Phys. 15 4582
Google Scholar
[16] Tichý L, Tichá H 1995 J. Non-Cryst. Solids 189 141
Google Scholar
[17] Xia F, Baccaro S, Zhao D, Falconieri M, Chen G 2005 Nucl. Instrum. Methods Phys. Res. B 234 525
Google Scholar
[18] Sharma E, Sharma R, Sharma V, Sharma P 2018 AIP Conf. Proc. 2050 020008
[19] Zha C, Wang R, Smith A, Prasad A, Jarvis R A, Luther-Davies B 2007 J. Mater. Sci-Mater. El. 18 389
Google Scholar
[20] Arsova D 1996 J. Phys. Chem. Solids 57 1279
Google Scholar
[21] Fouad S S 1999 Vacuum 52 505
Google Scholar
[22] Cheng C, Wang X S, Xu T F, Sun L H, Pan Z H, Liu S, Zhu Q D, Liao F X, Nie Q H, Dai S X, Shen X H, Zhang X H, Chen W 2016 Infrared Phys. Techn. 76 698
Google Scholar
[23] Abd El-Rahman A A, Eid A, Sanad M, El-Ocker R 1998 J. Phys. Chem. Solids 59 825
Google Scholar
[24] Sharma P, Katyal S C 2008 J. Non-Cryst. Solids 354 3836
Google Scholar
[25] Gonçalves C, Mereau R, Nazabal V, Boussard-Pledel C, Roiland C, Furet E, Deschamps M, Bureau B, Dussauze M 2021 J. Solid State Chem. 297 122062
Google Scholar
[26] Hassanien A S, Sharma I, Akl A A 2020 J. Non-Cryst. Solids 531 119853
Google Scholar
[27] Knotek P, Kutalek P, Cernoskova E, Vlcek M, Tichy L 2020 RSC Adv. 10 42744
Google Scholar
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