Morphology engineering of self-assembled porous zinc manganate hexagons for lithium ion storage

Porous zinc manganate (ZnMn2O4), which is typically fabricated from the decomposition of its carbonates, promises a high-performance anode material for lithium ion batteries (LIBs). Most of porous ZnMn2O4 in literature presents in sphere morphology. Herein, a unique type of porous ZnMn2O4 hexagons w...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Electrochimica acta 2020-01, Vol.330, p.135260, Article 135260
Hauptverfasser: Cao, Huili, Xiao, Xinxin, Wang, Xinzhen, Liu, Jiurong, Si, Pengchao
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Porous zinc manganate (ZnMn2O4), which is typically fabricated from the decomposition of its carbonates, promises a high-performance anode material for lithium ion batteries (LIBs). Most of porous ZnMn2O4 in literature presents in sphere morphology. Herein, a unique type of porous ZnMn2O4 hexagons with a side length of about 2 μm and a BET specific surface area of 34.19 m2 g−1, assembled by ca. 100 nm nanoparticles, has been successfully fabricated by a solvothermal reaction with subsequent calcination of the self-assembled catena-poly intermediates. The growth mechanism of the solvothermal products has been systematically investigated by adjusting the stoichiometric ratio of oxalic acid, the type of the salt source and acid additive, and the reaction media, resulting in a wide spectrum of morphologies ranging from hexagon, porous sphere, hourglass to belt. The hexagon precursor was calcined in air to obtain the porous structure, attributed to the spaces between nanoparticle assemblies. When used for lithium-ion storage, the as-prepared porous ZnMn2O4 hexagons-based anode exhibits a reversible capacity of 716 mA h g−1 after 200 cycles at 100 mA g−1, outperforming the pure porous Mn2O3 hexagons and the non-porous ZnMn2O4 hexagons. [Display omitted]
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2019.135260