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Journal articles on the topic 'Ag2TeNW'

Author: Grafiati

Published: 6 September 2023

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1

Klein, Wilhelm, Jan Curda, Eva-Maria Peters, and Martin Jansen. "Disilberoxotellurat(VI), Ag2TeO4." Zeitschrift f�r anorganische und allgemeine Chemie 631, no. 4 (March 2005): 723–27. http://dx.doi.org/10.1002/zaac.200400457.

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2

El Zaibani, M. El Zaibani, A. Altawaf Altawaf, and E. F. El Agammyc. "Tracking of Formed Crystalline Phases in the Binary Silver Tellurite Glass-ceramics." مجلة جامعة عمران 3, no. 5 (June 24, 2023): 12. http://dx.doi.org/10.59145/jaust.v3i5.56.

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Glasses and glass-ceramics based on silver tellurite system xAg2O·(100-x)TeO2 (0 £ x £ 60 mol%) were prepared by melt-quenching method. The structure of the studied glasses and glass-ceramics was investigated by several techniques. XRD patterns reveal the existence of only one glassy region at 20 < x ≤ 30 mol% with two crystalline a-TeO2 and Ag2TeO3 phases that formed separately in the prepared samples below 20 and beyond 30 mol% Ag2O, respectively. The peaks intensity corresponding to the crystalline a-TeO2 and Ag2TeO3 phases was found to decrease and increase with Ag2O content, respectively. This may be correlated with changes in the concentration of and units that, respectively, build up the crystalline a-TeO2 and Ag2TeO3 phases. In the glassy region, there is no crystalline phase, which may be attributed to the abundance of the deformed units that build up the glassy phase, and the concentrations of and units are neglected in this region. SEM and TEM micrographs and the related electron diffraction patterns (EDP) confirmed the formation of crystallized clusters in Ag2O-rich glasses.

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3

Su, Xin, Yuan Gao, Qi Wu, Haizeng Song, Shancheng Yan, and Yi Shi. "Robust UV Plasmonic Properties of Co-Doped Ag2Te." Crystals 12, no. 10 (October 17, 2022): 1469. http://dx.doi.org/10.3390/cryst12101469.

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Ag2Te is a novel topological insulator system and a new candidate for plasmon resonance due to the existence of a Dirac cone in the low-energy region. Although the optical response spectrum of Ag2Te has been studied by theoretical and experimental methods, the plasmon resonance and stability of Co-doped Ag2Te remain elusive. Here, we theoretically report a new unconventional UV plasmon mode and its stability in Co-doped Ag2Te. Through density functional theory (DFT), we identify a deep UV plasmon mode within 15–40 eV, which results from the enhanced inter-band transition in this range. The deep UV plasmon is important for detection and lithography, but they have previously been difficult to obtain with traditional plasmon materials such as noble metals and graphene, while most of which only support plasmons in the visible and infrared spectra. Furthermore, we should highlight that the high-energy dielectric function is almost invariant under different doping amounts, indicating that the UV plasmon of Ag2Te is robust under Co doping. Our results predict a spectrum window of a robust deep UV plasmon mode for Ag2Te-related material systems.

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4

Ragimov, S. S., M. A. Musayev, and N. N. Hashimova. "Transport properties of (AgSbТe₂)_0.7(PbTe)_0.3 thermoelectric compound." Low Temperature Physics 48, no. 10 (October 2022): 787–90. http://dx.doi.org/10.1063/10.0014020.

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Transport properties, namely electrical conductivity, Seebeck and Hall coefficients, and thermal conductivity, were measured from 80 to 560 K. The phase transition at about 410 K, representing the phase transition from α-Ag2Te to β-Ag2Te, influences the electrical transport properties. The temperature dependence of Hall coefficient passes through a maximum ∼200 K and has a negative sign. It is shown that these peculiarities are due to the presence of Ag2Te phase.

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5

Lee, Sunghun, Ho Sun Shin, Jae Yong Song, and Myung-Hwa Jung. "Thermoelectric Properties of a Single Crystalline Ag2Te Nanowire." Journal of Nanomaterials 2017 (2017): 1–5. http://dx.doi.org/10.1155/2017/4308968.

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Silver chalcogenides have received much attention in potential thermoelectric materials research because of high carrier mobility and low effective mass. Among them, in Ag2Te, it was reported that the phase transition from monoclinic to cubic phase occurs at relatively low temperatures, so that extensive research for effective application using this material has been aroused. In this work, we investigated how 1-dimensional nanostructure affects the thermoelectric properties through as-synthesized single crystalline Ag2Te nanowires. Adopting well-defined thermoelectric MEMS device structure and transferring an individual Ag2Te nanowire, we measure electrical resistance and Seebeck coefficient as a function of temperature. When the phase changes from monoclinic to cubic, the resistance increases, while absolute Seebeck coefficient value decreases. These results are compared with previous reports for Ag2Te bulk and film, suggesting the increased density of states of the carriers due to nanowire structure.

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6

Uruno, Aya, and Masakazu Kobayashi. "Formation of AgGaTe2 films from (Ag2Te+Ga2Te3)/Ag2Te or Ga2Te3/Ag2Te bilayer structures." AIP Advances 8, no. 11 (November 2018): 115023. http://dx.doi.org/10.1063/1.5039992.

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7

Pandiaraman, M., N. Soundararajan, and R. Ganesan. "Optical Studies of Physically Deposited Nano-Ag₂Te Thin Films." Defect and Diffusion Forum 319-320 (October 2011): 185–92. http://dx.doi.org/10.4028/www.scientific.net/ddf.319-320.185.

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Silver telluride (Ag2Te), I-VI semiconductor compound with potential applications in various advanced fields. Ag2Te nano films of thickness between 16 nm and 145 nm prepared by thermal evaporation technique at high vacuum better than 2x105 mbar. These films are found to exhibit polycrystalline nature with monoclinic structure from their XRD studies. The average particle size of these films are found to be around 24 nm using the Debye-Scherrer’s formula From AFM measurements, the average particle size is around 24 nm. The emission spectra of these films were recorded and analysed to determine its optical band gap. Optical band gap of Ag2Te varies from 1.6 eV to 1.8 eV with respect to their corresponding thicknesses of films.

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8

Moroz, Mykola, Fiseha Tesfaye, Pavlo Demchenko, Myroslava Prokhorenko, Nataliya Yarema, Daniel Lindberg, Oleksandr Reshetnyak, and Leena Hupa. "The Equilibrium Phase Formation and Thermodynamic Properties of Functional Tellurides in the Ag–Fe–Ge–Te System." Energies 14, no. 5 (February 28, 2021): 1314. http://dx.doi.org/10.3390/en14051314.

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Equilibrium phase formations below 600 K in the parts Ag2Te–FeTe2–F1.12Te–Ag2Te and Ag8GeTe6–GeTe–FeTe2–AgFeTe2–Ag8GeTe6 of the Fe–Ag–Ge–Te system were established by the electromotive force (EMF) method. The positions of 3- and 4-phase regions relative to the composition of silver were applied to express the potential reactions involving the AgFeTe2, Ag2FeTe2, and Ag2FeGeTe4 compounds. The equilibrium synthesis of the set of phases was performed inside positive electrodes (PE) of the electrochemical cells: (−)Graphite ‖LE‖ Fast Ag+ conducting solid-electrolyte ‖R[Ag+]‖PE‖ Graphite(+), where LE is the left (negative) electrode, and R[Ag+] is the buffer region for the diffusion of Ag+ ions into the PE. From the observed results, thermodynamic quantities of AgFeTe2, Ag2FeTe2, and Ag2FeGeTe4 were experimentally determined for the first time. The reliability of the division of the Ag2Te–FeTe2–F1.12Te–Ag2Te and Ag8GeTe6–GeTe–FeTe2–AgFeTe2–Ag8GeTe6 phase regions was confirmed by the calculated thermodynamic quantities of AgFeTe2, Ag2FeTe2, and Ag2FeGeTe4 in equilibrium with phases in the adjacent phase regions. Particularly, the calculated Gibbs energies of Ag2FeGeTe4 in two different adjacent 4-phase regions are consistent, which also indicates that it has stoichiometric composition.

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9

Som, Anirban, and T. Pradeep. "Heterojunction double dumb-bell Ag2Te–Te–Ag2Te nanowires." Nanoscale 4, no. 15 (2012): 4537. http://dx.doi.org/10.1039/c2nr30730h.

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10

Ali, Liqaa S., and Aliyah A. Shihab. "Ag2Te thin films' structural and optical characteristics as a result of Al doping." Journal of Ovonic Research 19, no. 4 (August 2023): 433–38. http://dx.doi.org/10.15251/jor.2023.194.433.

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During the course of this investigation, Ag2Te and Al-doped Ag2Te films' structural and optical properties at various concentrations (1%, 1.5%) are examined. The thermal evaporation method was used to deposit 400-nm thick Ag2Te thin films on glass substrates at 100 °C. The structure is monoclinic of the polycrystalline films were revealed by (XRD). Between 1 and 1.5%, the activated precursor did not vary with respect to the favored direction. According to the XRD results, the mean crystal sizes ranged from 25.62 to 37.13 nm. The surface of the film is incredibly smooth, according to atomic force microscope study (AFM). The produced films' optical characteristics were investigated. optical absorption coefficient (α) of films were determined using the absorption spectra within the wavelength region (400-1000) nm. It was discovered that the optical energy gap allows direct transmission and that it narrows with doping.. AFM was used to measure the grain size and roughness, which change when impurities are added.

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11

Vassilev, V., V. Parvanova, and V. Vatchkov. "Phase equilibria in the Ag2Te-ZnTe and Ag2Te-Zn systems." Journal of Thermal Analysis and Calorimetry 83, no. 2 (February 2006): 467–73. http://dx.doi.org/10.1007/s10973-005-6942-y.

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12

Sakuma, Takashi, and Shoji Saitoh. "Structure of α-Ag2Te." Journal of the Physical Society of Japan 54, no. 9 (September 15, 1985): 3647–48. http://dx.doi.org/10.1143/jpsj.54.3647.

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13

Bürgermeister, A., and W. Sitte. "Chemical diffusion in β-Ag2Te." Solid State Ionics 141-142 (May 2001): 331–34. http://dx.doi.org/10.1016/s0167-2738(01)00745-7.

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14

KOBAYASHI, M. "Caterpillar motion in $alpha;-Ag2Te." Solid State Ionics 40-41 (August 1990): 300–302. http://dx.doi.org/10.1016/0167-2738(90)90345-r.

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15

Manzoor, Saima, Yumin Liu, Zhongyuan Yu, Xiuli Fu, and Guijun Ban. "Hydrothermal Synthesis and Mechanism of Unusual Zigzag Ag2Te and Ag2Te/C Core-Shell Nanostructures." Journal of Nanomaterials 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/350981.

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A single step surfactant-assisted hydrothermal route has been developed for the synthesis of zigzag silver telluride nanowires with diameter of 50–60 nm and length of several tens of micrometers. Silver nitrate (AgNO3) and sodium tellurite (Na2TeO3), are the precursors and polyvinylpyrrolidone (PVP) is used as surfactant in the presence of the reducing agent, that is, hydrazine hydrate (N2H4·H2O). In addition to the zigzag nanowires a facile hydrothermal reduction-carbonization route is proposed for the preparation of uniform core-shell Ag2Te/C nanowires. In case of Ag2Te/C synthesis process the same precursors are employed for Ag and Te along with the ethylene glycol used as reducing agent and glucose as the carbonizing agent. Morphological and compositional properties of the prepared products are analyzed with the help of scanning electron microscopy, transmission electron microscopy, and energy dispersive X-ray spectroscopy, respectively. The detailed formation mechanism of the zigzag morphology and reduction-carbonization growth mechanism for core-shell nanowires are illustrated on the bases of experimental results.

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16

Hirata, Keisuke, Kentaro Kuga, Masaharu Matsunami, Minyue Zhu, Joseph P. Heremans, and Tsunehiro Takeuchi. "Magneto-thermal conductivity effect and enhanced thermoelectric figure of merit in Ag₂Te." AIP Advances 13, no. 1 (January 1, 2023): 015016. http://dx.doi.org/10.1063/5.0131326.

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In this study, we report a large magneto-thermal conductivity effect, potentially usable in heat flow switches and thermoelectric devices, in Ag2Te over a wide temperature range, including room temperature. When a magnetic field of μ0 H = 9 T is applied to Ag2Te at 300 K along the direction perpendicular to the heat and electric currents, the thermal conductivity κ decreases by a remarkable 61%. This effect is mainly caused by the suppressed electronic thermal conductivity in association with a significant magnetoresistance effect, but the suppression of the thermal conductivity is larger than that of the electrical conductivity, presumably due to a field-induced decrease in the Lorenz ratio. Its very low lattice thermal conductivity, as low as 0.5 W m−1 K−1, also greatly contributes to the large relative magneto-thermal conductivity effect. The significant decrease in thermal conductivity and the 18% increase in the Seebeck coefficient S lead to a nearly 100% increase in the thermoelectric figure of merit zT = S2 σTκ−1 despite the 43% decrease in electrical conductivity σ.

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17

Aliyev, F. F., M. B. Jafarov, V. I. Eminova, G. Z. Asgerova, and R. A. Hasanova. "Resonance Scattering of Electrons in Ag2Te." Acta Physica Polonica A 120, no. 6 (December 2011): 1061–64. http://dx.doi.org/10.12693/aphyspola.120.1061.

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18

González-Ibarra, A. A., F. Nava-Alonso, and A. Uribe-Salas. "Cyanidation kinetics of silver telluride (Ag2Te)." Canadian Metallurgical Quarterly 56, no. 3 (July 3, 2017): 272–80. http://dx.doi.org/10.1080/00084433.2017.1350391.

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19

Lin, Zong-Hong, Zih-Yu Shih, Prathik Roy, and Huan-Tsung Chang. "Preparation of Photocatalytic Au-Ag2Te Nanomaterials." Chemistry - A European Journal 18, no. 39 (August 21, 2012): 12330–36. http://dx.doi.org/10.1002/chem.201201414.

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20

Chang, Yi, Jun Guo, Yun-Qiao Tang, Yi-Xing Zhang, Jing Feng, and Zhen-Hua Ge. "Facile synthesis of Ag2Te nanowires and thermoelectric properties of Ag2Te polycrystals sintered by spark plasma sintering." CrystEngComm 21, no. 11 (2019): 1718–27. http://dx.doi.org/10.1039/c8ce01863d.

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21

Aliev, F. F., E. M. Kerimova, and S. A. Aliev. "Electrical and thermoelectric properties of p-Ag2Te." Semiconductors 36, no. 8 (August 2002): 869–73. http://dx.doi.org/10.1134/1.1500462.

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22

Ohno, Satoru, Masaki Togashi, Adrian C. Barnes, and John E. Enderby. "Electrical Properties of Molten AgCl–Ag2Te Mixtures." Journal of the Physical Society of Japan 68, no. 7 (July 15, 1999): 2338–43. http://dx.doi.org/10.1143/jpsj.68.2338.

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23

Aliev, F. F., and M. B. Jafarov. "Energy spectrum of charge carriers in Ag2Te." Semiconductors 42, no. 11 (November 2008): 1270–73. http://dx.doi.org/10.1134/s1063782608110043.

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24

Aliyev, S. A., Z. F. Agayev, and R. I. Selimzadeh. "Energy spectrum of charge carriers in Ag2Te." Semiconductors 42, no. 12 (December 2008): 1383–87. http://dx.doi.org/10.1134/s1063782608120026.

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25

Bahari, Zahra, Jacques Rivet, and Jérôme Dugué. "Diagramme de phases du système Ag2Te-In2Te3." Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry 1, no. 7 (July 1998): 411–15. http://dx.doi.org/10.1016/s1387-1609(98)80420-9.

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26

Chen, Sinn-wen, Ting-ruei Yang, Haw-wen Hsiao, Po-han Lin, Jia-hong Huang, and Jenn-dong Huang. "Ni/Te and Ni/Ag2Te interfacial reactions." Materials Chemistry and Physics 180 (September 2016): 396–403. http://dx.doi.org/10.1016/j.matchemphys.2016.06.023.

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27

Chayasombat, Bralee, Suparoek Henpraserttae, Chris Boothroyd, and Chanchana Thanachayanont. "Mechanically alloyed β-Ag2Te in thermoelectric Bi2Se0.01Te2.99." Materials Letters 116 (February 2014): 243–46. http://dx.doi.org/10.1016/j.matlet.2013.11.048.

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28

Vassilev, V., Z. Boncheva-Mladenova, Pl Patev, and S. Aleksandrova. "Phase equilibria in the Ag2Te-Cd system." Journal of Thermal Analysis 33, no. 3 (September 1988): 609–13. http://dx.doi.org/10.1007/bf02138562.

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29

Sakakibara, Tsutomu, Yasuo Takigawa, and Kou Kurosawa. "Hall Mobility Enhancement in AgBiTe2–Ag2Te Composites." Japanese Journal of Applied Physics 41, Part 1, No. 5A (May 15, 2002): 2842–44. http://dx.doi.org/10.1143/jjap.41.2842.

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30

Gawel, W., E. Zaleska, and J. Terpiłowski. "Phase equilibria in the Tl2Te-Ag2Te system." Journal of Thermal Analysis 32, no. 1 (January 1987): 227–35. http://dx.doi.org/10.1007/bf01914564.

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31

Marin, Rose Marie, G�rard Brun, and Jean Claude Tedenac. "Phase equilibria in the Sb2Te3-Ag2Te system." Journal of Materials Science 20, no. 2 (February 1985): 730–35. http://dx.doi.org/10.1007/bf01026548.

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32

Fujikane, Masaki, Ken Kurosaki, Hiroaki Muta, and Shinsuke Yamanaka. "Electrical properties of α- and β-Ag2Te." Journal of Alloys and Compounds 387, no. 1-2 (January 2005): 297–99. http://dx.doi.org/10.1016/j.jallcom.2004.06.054.

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33

Fujikane, Masaki, Ken Kurosaki, Hiroaki Muta, and Shinsuke Yamanaka. "Thermoelectric properties of α- and β-Ag2Te." Journal of Alloys and Compounds 393, no. 1-2 (May 2005): 299–301. http://dx.doi.org/10.1016/j.jallcom.2004.10.002.

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34

Zhu, Ting, Xianli Su, Qingjie Zhang, and Xinfeng Tang. "Structural transformation and thermoelectric performance in Ag2Te1−Se solid solution." Journal of Alloys and Compounds 871 (August 2021): 159507. http://dx.doi.org/10.1016/j.jallcom.2021.159507.

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35

SAKAKIBARA, Tsutomu, Yasuo TAKIGAWA, Akihiro KAMEYAMA, and Kou KUROSAWA. "Improvement of Thermoelectric Properties by Dispersing Ag2Te Grains in AgBiTe2 Matrix: Composition Effects in (AgBiTe2)1-x(Ag2Te)x." Journal of the Ceramic Society of Japan 110, no. 1280 (2002): 259–63. http://dx.doi.org/10.2109/jcersj.110.259.

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36

Sutch, Tabitha, Jared M. Allred, and Greg Szulczewski. "Electron conducting Ag2Te nanowire/polymer thermoelectric thin films." Journal of Vacuum Science & Technology A 39, no. 2 (March 2021): 023401. http://dx.doi.org/10.1116/6.0000690.

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37

Zuo, Pengfei, Shengyi Zhang, Baokang Jin, Yupeng Tian, and Jiaxiang Yang. "Rapid Synthesis and Electrochemical Property of Ag2Te Nanorods." Journal of Physical Chemistry C 112, no. 38 (August 29, 2008): 14825–29. http://dx.doi.org/10.1021/jp804164h.

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38

Babanly, D. M., I. I. Aliev, K. N. Babanly, and Yu A. Yusibov. "Phase equilibria in the Ag2Te-PbTe-Bi2Te3 system." Russian Journal of Inorganic Chemistry 56, no. 9 (September 2011): 1472–77. http://dx.doi.org/10.1134/s0036023611090038.

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39

Aliev, S. A., F. F. Aliev, and Z. S. Gasanov. "Thermodynamic parameters of diffuse phase transitions in Ag2Te." Physics of the Solid State 40, no. 9 (September 1998): 1540–43. http://dx.doi.org/10.1134/1.1130593.

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40

Kakinuma, F., Y. Tsuchiya, and K. Suzuki. "Critical sound propagation in liquid Ag–Ag2Te alloys." Journal of Non-Crystalline Solids 250-252 (August 1999): 373–76. http://dx.doi.org/10.1016/s0022-3093(99)00267-7.

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41

van der Lee, A., and J. L. de Boer. "Redetermination of the structure of hessite, Ag2Te-III." Acta Crystallographica Section C Crystal Structure Communications 49, no. 8 (August 15, 1993): 1444–46. http://dx.doi.org/10.1107/s0108270193003294.

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42

Tomari, T. "Caterpillar motion of silver ions in α-Ag2Te." Solid State Ionics 35, no. 3-4 (September 1989): 355–58. http://dx.doi.org/10.1016/0167-2738(89)90321-4.

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43

OKAZAKI, H. "A cooperative motion of cations in $alpha;-Ag2Te." Solid State Ionics 40-41 (August 1990): 171–74. http://dx.doi.org/10.1016/0167-2738(90)90314-h.

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44

Suchand Sandeep, C. S., A. K. Samal, T. Pradeep, and Reji Philip. "Optical limiting properties of Te and Ag2Te nanowires." Chemical Physics Letters 485, no. 4-6 (January 2010): 326–30. http://dx.doi.org/10.1016/j.cplett.2009.12.065.

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45

Sugar, Joshua D., and Douglas L. Medlin. "Precipitation of Ag2Te in the thermoelectric material AgSbTe2." Journal of Alloys and Compounds 478, no. 1-2 (June 2009): 75–82. http://dx.doi.org/10.1016/j.jallcom.2008.11.054.

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46

Jiang, L., and E. R. Nowak. "Electrical noise in n- and p-type Ag2Te." Applied Physics Letters 83, no. 3 (July 21, 2003): 503–5. http://dx.doi.org/10.1063/1.1593820.

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47

Tachibana, F., Y. Sakai, and H. Okazaki. "Correlation factor of tracer diffusion in alpha -Ag2Te." Journal of Physics: Condensed Matter 4, no. 46 (November 16, 1992): 8989–96. http://dx.doi.org/10.1088/0953-8984/4/46/006.

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48

Sakuma, T., T. Aoyama, H. Takahashi, Y. Shimojo, and Y. Morii. "Diffuse neutron scattering from superionic phase of Ag2Te." Solid State Ionics 86-88 (July 1996): 227–30. http://dx.doi.org/10.1016/0167-2738(96)00130-0.

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49

Lensch-Falk, J. L., J. D. Sugar, M. A. Hekmaty, and D. L. Medlin. "Morphological evolution of Ag2Te precipitates in thermoelectric PbTe." Journal of Alloys and Compounds 504, no. 1 (August 2010): 37–44. http://dx.doi.org/10.1016/j.jallcom.2010.05.054.

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50

Lin, Zong-Hong, Zih-Yu Shih, Prathik Roy, and Huan-Tsung Chang. "ChemInform Abstract: Preparation of Photocatalytic Au-Ag2Te Nanomaterials." ChemInform 44, no. 2 (January 8, 2013): no. http://dx.doi.org/10.1002/chin.201302178.

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