B. D. Igamov, A. I. Kamardin, D. Kh. Nabiev, I. R. Bekpulatov, G. T. Imanova, A. S. Kosimov, B. D. Donaev, A. M. Normamatov, S. H. Jabarov, Y. I. Aliyev
{"title":"用x射线衍射仪研究热等静压和火花等离子烧结方法制备的Mn4Si7硅化物晶体","authors":"B. D. Igamov, A. I. Kamardin, D. Kh. Nabiev, I. R. Bekpulatov, G. T. Imanova, A. S. Kosimov, B. D. Donaev, A. M. Normamatov, S. H. Jabarov, Y. I. Aliyev","doi":"10.1186/s40712-025-00265-0","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, the physical and structural properties of Mn₄Si₇ silicide crystals synthesized using Hot Isostatic Pressing (HIP) and Spark Plasma Sintering (SPS) methods were analyzed using X-ray diffraction (XRD) techniques. In the samples obtained by the HIP method, 11 diffraction peaks were identified, with crystal sizes ranging from 8.8∙10⁻⁹ m to 3.6∙10⁻⁸ m, and the lattice strain index varied from 0.01 to 0.41. These results reflect the microstructural characteristics and the deformation of the crystals, providing insight into how these structural features influence the mechanical, thermal, and electronic properties of the material. In the SPS method samples, 13 diffraction peaks were observed, with crystal sizes ranging from 3.8∙10⁻⁹ m to 3.6∙10⁻⁸ m, and lattice strain varied from 0.002 to 0.19, indicating that the crystals maintain structural equilibrium and geometric integrity. The dislocation density, measured in the HIP samples (ranging from 3.5∙10<sup>1</sup>⁰ to 3.2∙10<sup>12</sup>) and SPS samples (ranging from 7.4∙10<sup>11</sup> to 7.9∙10<sup>14</sup>), plays a crucial role in determining the crystals' plasticity and mechanical strength. The degree of crystallinity was found to be 6.4% for the HIP method and 7% for the SPS method, reflecting the structural purity and perfection of the crystals. IR transmission spectra revealed structural changes in the crystals, demonstrating their direct influence on the material's electronic and optical properties. These analyses provide valuable insights into enhancing the thermoelectric properties and mechanical stability of materials, as well as improving the performance of technological devices under high-temperature and high-pressure conditions. This study lays the foundation for future research aimed at optimizing material properties for advanced technological applications.</p></div>","PeriodicalId":592,"journal":{"name":"International Journal of Mechanical and Materials Engineering","volume":"20 1","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://jmsg.springeropen.com/counter/pdf/10.1186/s40712-025-00265-0","citationCount":"0","resultStr":"{\"title\":\"Study of Mn4Si7 silicide crystals obtained by hot isostatic pressing and spark plasma sintering methods in an X-ray diffractometer\",\"authors\":\"B. D. Igamov, A. I. Kamardin, D. Kh. Nabiev, I. R. Bekpulatov, G. T. Imanova, A. S. Kosimov, B. D. Donaev, A. M. Normamatov, S. H. Jabarov, Y. I. Aliyev\",\"doi\":\"10.1186/s40712-025-00265-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In this study, the physical and structural properties of Mn₄Si₇ silicide crystals synthesized using Hot Isostatic Pressing (HIP) and Spark Plasma Sintering (SPS) methods were analyzed using X-ray diffraction (XRD) techniques. In the samples obtained by the HIP method, 11 diffraction peaks were identified, with crystal sizes ranging from 8.8∙10⁻⁹ m to 3.6∙10⁻⁸ m, and the lattice strain index varied from 0.01 to 0.41. These results reflect the microstructural characteristics and the deformation of the crystals, providing insight into how these structural features influence the mechanical, thermal, and electronic properties of the material. In the SPS method samples, 13 diffraction peaks were observed, with crystal sizes ranging from 3.8∙10⁻⁹ m to 3.6∙10⁻⁸ m, and lattice strain varied from 0.002 to 0.19, indicating that the crystals maintain structural equilibrium and geometric integrity. The dislocation density, measured in the HIP samples (ranging from 3.5∙10<sup>1</sup>⁰ to 3.2∙10<sup>12</sup>) and SPS samples (ranging from 7.4∙10<sup>11</sup> to 7.9∙10<sup>14</sup>), plays a crucial role in determining the crystals' plasticity and mechanical strength. The degree of crystallinity was found to be 6.4% for the HIP method and 7% for the SPS method, reflecting the structural purity and perfection of the crystals. IR transmission spectra revealed structural changes in the crystals, demonstrating their direct influence on the material's electronic and optical properties. These analyses provide valuable insights into enhancing the thermoelectric properties and mechanical stability of materials, as well as improving the performance of technological devices under high-temperature and high-pressure conditions. This study lays the foundation for future research aimed at optimizing material properties for advanced technological applications.</p></div>\",\"PeriodicalId\":592,\"journal\":{\"name\":\"International Journal of Mechanical and Materials Engineering\",\"volume\":\"20 1\",\"pages\":\"\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-03-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://jmsg.springeropen.com/counter/pdf/10.1186/s40712-025-00265-0\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Mechanical and Materials Engineering\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.1186/s40712-025-00265-0\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Mechanical and Materials Engineering","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1186/s40712-025-00265-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Study of Mn4Si7 silicide crystals obtained by hot isostatic pressing and spark plasma sintering methods in an X-ray diffractometer
In this study, the physical and structural properties of Mn₄Si₇ silicide crystals synthesized using Hot Isostatic Pressing (HIP) and Spark Plasma Sintering (SPS) methods were analyzed using X-ray diffraction (XRD) techniques. In the samples obtained by the HIP method, 11 diffraction peaks were identified, with crystal sizes ranging from 8.8∙10⁻⁹ m to 3.6∙10⁻⁸ m, and the lattice strain index varied from 0.01 to 0.41. These results reflect the microstructural characteristics and the deformation of the crystals, providing insight into how these structural features influence the mechanical, thermal, and electronic properties of the material. In the SPS method samples, 13 diffraction peaks were observed, with crystal sizes ranging from 3.8∙10⁻⁹ m to 3.6∙10⁻⁸ m, and lattice strain varied from 0.002 to 0.19, indicating that the crystals maintain structural equilibrium and geometric integrity. The dislocation density, measured in the HIP samples (ranging from 3.5∙101⁰ to 3.2∙1012) and SPS samples (ranging from 7.4∙1011 to 7.9∙1014), plays a crucial role in determining the crystals' plasticity and mechanical strength. The degree of crystallinity was found to be 6.4% for the HIP method and 7% for the SPS method, reflecting the structural purity and perfection of the crystals. IR transmission spectra revealed structural changes in the crystals, demonstrating their direct influence on the material's electronic and optical properties. These analyses provide valuable insights into enhancing the thermoelectric properties and mechanical stability of materials, as well as improving the performance of technological devices under high-temperature and high-pressure conditions. This study lays the foundation for future research aimed at optimizing material properties for advanced technological applications.