A soft chemistry approach to preparing (de)sodiated transition-metal hydroxy molybdates
العنوان: | A soft chemistry approach to preparing (de)sodiated transition-metal hydroxy molybdates |
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المؤلفون: | Guilherme M. Martins, Roberto L. Moreira, Anderson Dias |
المصدر: | CrystEngComm. 22:1939-1955 |
بيانات النشر: | Royal Society of Chemistry (RSC), 2020. |
سنة النشر: | 2020 |
مصطلحات موضوعية: | Coprecipitation, chemistry.chemical_element, 02 engineering and technology, General Chemistry, Triclinic crystal system, Molybdate, 010402 general chemistry, 021001 nanoscience & nanotechnology, Condensed Matter Physics, 01 natural sciences, Soft chemistry, Hydrothermal circulation, 0104 chemical sciences, Nickel, symbols.namesake, chemistry.chemical_compound, chemistry, Transition metal, symbols, General Materials Science, 0210 nano-technology, Raman spectroscopy, Nuclear chemistry |
الوصف: | A soft chemistry approach was applied to synthesize de(sodiated) transition-metal hydroxy molybdates under hydrothermal conditions. Different NaM2(H3O2)(MoO4)2 and M2MoO4(OH)2 compositions (M = Ni, Zn) were prepared at mild temperatures (110–250 °C) for times ranging from 10 min to 24 h. Sodiated compounds were obtained after a microwave-assisted hydrothermal process at 150 °C (10–120 min) for zinc-based materials. Besides, conventional heating destabilized the sodiated NaZn2(H3O2)(MoO4)2 phase at 110 °C, thus increasing the amount of Zn2MoO4(OH)2 at temperatures up to 250 °C. NaNi2(H3O2)(MoO4)2 phases were noted only for 10 min under microwave irradiation, while longer times promoted a chemical reaction towards a new desodiated phase. This novel Ni2MoO4(OH)2 phase was also obtained by conventional hydrothermal processing (110–250 °C, 24 h). Slow precipitation rates yielded a hydrated nickel molybdate (triclinic, P) after coprecipitation followed or not by microwave irradiation. Raman spectroscopy analysis results showed a good agreement with experimental results and group-theory calculations for both sodiated and desodiated materials. A temperature-induced polymorphic transformation was observed from NiMoO4·xH2O (triclinic, P) to α-NiMoO4 (monoclinic, C2/m). For all the obtained polymorphs, the relevant Raman modes were depicted, allowing us to determine their spectroscopic fingerprints. The results constitute an important basis on the understanding of the synthesis of (de)sodiated transition-metal hydroxy molybdates under hydrothermal conditions. |
تدمد: | 1466-8033 |
DOI: | 10.1039/c9ce01554j |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::638e57216a928231b92b4b5163a4bc0d https://doi.org/10.1039/c9ce01554j |
Rights: | CLOSED |
رقم الانضمام: | edsair.doi...........638e57216a928231b92b4b5163a4bc0d |
قاعدة البيانات: | OpenAIRE |
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Different NaM2(H3O2)(MoO4)2 and M2MoO4(OH)2 compositions (M = Ni, Zn) were prepared at mild temperatures (110–250 °C) for times ranging from 10 min to 24 h. Sodiated compounds were obtained after a microwave-assisted hydrothermal process at 150 °C (10–120 min) for zinc-based materials. Besides, conventional heating destabilized the sodiated NaZn2(H3O2)(MoO4)2 phase at 110 °C, thus increasing the amount of Zn2MoO4(OH)2 at temperatures up to 250 °C. NaNi2(H3O2)(MoO4)2 phases were noted only for 10 min under microwave irradiation, while longer times promoted a chemical reaction towards a new desodiated phase. This novel Ni2MoO4(OH)2 phase was also obtained by conventional hydrothermal processing (110–250 °C, 24 h). Slow precipitation rates yielded a hydrated nickel molybdate (triclinic, P) after coprecipitation followed or not by microwave irradiation. 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