Continuous solid-phase synthesis of nanostructured lithium iron phosphate powders in air

Dettagli Bibliografici
Parent link:Ceramics International.— , 1981-
Vol. 44, iss. 7.— 2018.— [P. 1059-1065]
Autore principale: Kerbel B. M. Boris Moiseevich
Ente Autore: Национальный исследовательский Томский политехнический университет Школа базовой инженерной подготовки Отделение иностранных языков
Altri autori: Katsnelson L. M. Leonid Mikhaylovich, Falkovich Yu. V. Yulia Valerievna
Riassunto:Title screen
In this study, a cathode material based on LiFePO4/C is synthesised directly via continuous solid-phase synthesis in air without the need for an inert or reducing medium. A nanostructured dispersive crystal composite is formed during the direct synthesis of LiFePO4/C, and its role in determining the specific discharge capacity of the synthesised powder is considered. The nanostructured composites are formed by bottom-up self-assembly, resulting in dispersive, crystalline globular solids with well-developed internal porosity. The conditions created during the continuous synthesis of LiFePO4/C in air have a dominant influence on the morphologies of the nanostructured composites, which adopt ‘isometric’ or ‘platelet’ forms. In the latter case, three- and six-faced channels may develop within their volume. Increasing the concentration of these nanostructured composites within LiFePO4/C powders helps prevent degradation in the specific charge capacity and enhances their absolute values while cycling.
Режим доступа: по договору с организацией-держателем ресурса
Pubblicazione: 2018
Soggetti:
Accesso online:https://doi.org/10.1016/j.ceramint.2018.02.032
Natura: Elettronico Capitolo di libro
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=657599
Descrizione
Riassunto:Title screen
In this study, a cathode material based on LiFePO4/C is synthesised directly via continuous solid-phase synthesis in air without the need for an inert or reducing medium. A nanostructured dispersive crystal composite is formed during the direct synthesis of LiFePO4/C, and its role in determining the specific discharge capacity of the synthesised powder is considered. The nanostructured composites are formed by bottom-up self-assembly, resulting in dispersive, crystalline globular solids with well-developed internal porosity. The conditions created during the continuous synthesis of LiFePO4/C in air have a dominant influence on the morphologies of the nanostructured composites, which adopt ‘isometric’ or ‘platelet’ forms. In the latter case, three- and six-faced channels may develop within their volume. Increasing the concentration of these nanostructured composites within LiFePO4/C powders helps prevent degradation in the specific charge capacity and enhances their absolute values while cycling.
Режим доступа: по договору с организацией-держателем ресурса
DOI:10.1016/j.ceramint.2018.02.032