Hydrothermal synthesis of barium titanate nano/microrods and particle agglomerates using a sodium titanate precursor; Ceramics International; Vol. 47, iss. 7, Pt. A

Dades bibliogràfiques
Parent link:Ceramics International
Vol. 47, iss. 7, Pt. A.— 2021.— [P. 8904-8914]
Autor corporatiu: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий Научно-исследовательский центр "Физическое материаловедение и композитные материалы", Национальный исследовательский Томский политехнический университет Инженерная школа ядерных технологий Отделение ядерно-топливного цикла
Altres autors: Surmenev R. A. Roman Anatolievich, Chernozem R. V. Roman Viktorovich, Skirtach A. G. Andre, Bekareva A. S. Anastasiya Sergeevna, Leonova L. A. Liliya Aleksandrovna, Mathur S. Sanjay, Ivanov Yu. F. Yuriy Fedorovich, Surmeneva M. A. Maria Alexandrovna
Sumari:Title screen
The ion exchange processes and phase formation were studied by varying the properties of 1D barium titanate nanostructures. Temperature-, time- and alkalinity-dependent experiments were performed to study the BaTiO3 formation mechanism involving the generation of chemical sites which induced in situ transformation and dissolution-precipitation reactions occurring in a hydrothermal treatment procedure. As a result of the hydrothermal synthesis, BaTiO3 nano- and microrods with surface nanomaces and nanoparticle aggregates were formed in the temperature range of 160-210 °C, alkalinity range of 0.025-0.15 M and time range of 45-90 min. X-ray diffraction analysis revealed a significant increase in BaTiO3 material purity with increasing alkalinity from 0.025 to 0.15 M, even after a synthesis time of 45 min. In turn, Raman spectroscopy results showed that an increase in the synthesis time allowed not only BaTiO3 purity improvement, but also its phase composition control. The tetragonal phase of BaTiO3 was clearly observed after 6 h of hydrothermal synthesis at 210 °C and various alkalinities (from 0.025 to 0.15 M), while 45 and 90 min resulted in a mixture of cubic or tetragonal phases. Transmission electron microscopy demonstrated that BaTiO3 nanoparticles consisted of mainly tetragonal phases or a mixture of cubic and tetragonal phases, while BaTiO3 nano-/microrods preferably had cubic phases. Thus, variation of the temperature, time and alkalinity upon hydrothermal synthesis allowed the formation of BaTiO3 nano- and microstructures with different morphologies and phase compositions for diverse applications from biomedicine to microelectronics.
Режим доступа: по договору с организацией-держателем ресурса
Idioma:anglès
Publicat: 2021
Matèries:
Accés en línia:https://doi.org/10.1016/j.ceramint.2020.12.011
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=663852

MARC

LEADER 00000naa0a2200000 4500
001 663852
005 20250826101714.0
035 |a (RuTPU)RU\TPU\network\35022 
035 |a RU\TPU\network\34351 
090 |a 663852 
100 |a 20210312d2021 k||y0rusy50 ba 
101 0 |a eng 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Hydrothermal synthesis of barium titanate nano/microrods and particle agglomerates using a sodium titanate precursor  |f R. A. Surmenev, R. V. Chernozem, A. G. Skirtach [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 28 tit.] 
330 |a The ion exchange processes and phase formation were studied by varying the properties of 1D barium titanate nanostructures. Temperature-, time- and alkalinity-dependent experiments were performed to study the BaTiO3 formation mechanism involving the generation of chemical sites which induced in situ transformation and dissolution-precipitation reactions occurring in a hydrothermal treatment procedure. As a result of the hydrothermal synthesis, BaTiO3 nano- and microrods with surface nanomaces and nanoparticle aggregates were formed in the temperature range of 160-210 °C, alkalinity range of 0.025-0.15 M and time range of 45-90 min. X-ray diffraction analysis revealed a significant increase in BaTiO3 material purity with increasing alkalinity from 0.025 to 0.15 M, even after a synthesis time of 45 min. In turn, Raman spectroscopy results showed that an increase in the synthesis time allowed not only BaTiO3 purity improvement, but also its phase composition control. The tetragonal phase of BaTiO3 was clearly observed after 6 h of hydrothermal synthesis at 210 °C and various alkalinities (from 0.025 to 0.15 M), while 45 and 90 min resulted in a mixture of cubic or tetragonal phases. Transmission electron microscopy demonstrated that BaTiO3 nanoparticles consisted of mainly tetragonal phases or a mixture of cubic and tetragonal phases, while BaTiO3 nano-/microrods preferably had cubic phases. Thus, variation of the temperature, time and alkalinity upon hydrothermal synthesis allowed the formation of BaTiO3 nano- and microstructures with different morphologies and phase compositions for diverse applications from biomedicine to microelectronics. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Ceramics International 
463 |t Vol. 47, iss. 7, Pt. A  |v [P. 8904-8914]  |d 2021 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a hydrothermal synthesis 
610 1 |a barium titanate 
610 1 |a precursor 
610 1 |a microrods 
610 1 |a nanowires 
610 1 |a alkalinity 
610 1 |a гидротермальный синтез 
610 1 |a титанат бария 
610 1 |a нанопроволоки 
701 1 |a Surmenev  |b R. A.  |c physicist  |c Associate Professor of Tomsk Polytechnic University, Senior researcher, Candidate of physical and mathematical sciences  |f 1982-  |g Roman Anatolievich  |3 (RuTPU)RU\TPU\pers\31885  |9 15957 
701 1 |a Chernozem  |b R. V.  |c physicist  |c Associate Professor of Tomsk Polytechnic University  |f 1992-  |g Roman Viktorovich  |3 (RuTPU)RU\TPU\pers\36450  |9 19499 
701 1 |a Skirtach  |b A. G.  |g Andre 
701 1 |a Bekareva  |b A. S.  |g Anastasiya Sergeevna 
701 1 |a Leonova  |b L. A.  |c Chemical Engineer  |c Associate Professor of Tomsk Polytechnic University, Candidate of technical science  |f 1983-  |g Liliya Aleksandrovna  |3 (RuTPU)RU\TPU\pers\31564  |9 15724 
701 1 |a Mathur  |b S.  |g Sanjay 
701 1 |a Ivanov  |b Yu. F.  |c physicist  |c Professor of Tomsk Polytechnic University, Doctor of physical and mathematical sciences  |f 1955-  |g Yuriy Fedorovich  |3 (RuTPU)RU\TPU\pers\33559 
701 1 |a Surmeneva  |b M. A.  |c specialist in the field of material science  |c engineer-researcher of Tomsk Polytechnic University, Associate Scientist  |f 1984-  |g Maria Alexandrovna  |3 (RuTPU)RU\TPU\pers\31894  |9 15966 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Исследовательская школа химических и биомедицинских технологий  |b Научно-исследовательский центр "Физическое материаловедение и композитные материалы"  |3 (RuTPU)RU\TPU\col\24957 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Инженерная школа ядерных технологий  |b Отделение ядерно-топливного цикла  |3 (RuTPU)RU\TPU\col\23554 
801 2 |a RU  |b 63413507  |c 20210312  |g RCR 
850 |a 63413507 
856 4 |u https://doi.org/10.1016/j.ceramint.2020.12.011 
942 |c CF