差示扫描量热法
尖晶石
材料科学
金红石
离子
热稳定性
结晶学
化学
晶体结构
相(物质)
热力学
冶金
物理
有机化学
作者
Takuya Hatakeyama,Norihiko L. Okamoto,Tetsu Ichitsubo
标识
DOI:10.1016/j.jssc.2021.122683
摘要
This study reports thermal stability of α, β, γ, δ, and λ-type MnO2 polymorphs investigated using differential scanning calorimetry (DSC) and in-situ high-temperature X-ray diffraction measurement (HTXRD). These experiments revealed that the thermal stability of the polymorphs is in the following order: β > α > γ > δ ≈ λ. The β-MnO2 phase (1 × 1 tunnel, rutile structure), the most stable form between the MnO2 polymorphs, maintains the structure up to 500 °C until oxygen release causes phase transformation to Mn2O3. The α-MnO2 phase (2 × 2 and 1 × 1 tunnel structure) exhibits high thermal stability comparable to the β phase, despite its large vacant 2 × 2 tunnel. The γ-MnO2 phase (mixed microdomain structure of 2 × 1 tunnel and 1 × 1 tunnel) shows a stepwise transformation into β-MnO2 from 400 °C after structure relaxation. The δ-MnO2 phase (layered structure) is easily destabilized by extracting interlayer K ions, resultingly, to lose the interlayer periodicity below 200 °C, while each layer itself is preserved up to ∼500 °C. The λ-MnO2 phase (defect spinel structure) is thermally unstable and transforms into β-MnO2 around 250 °C, and subsequently decomposes to Mn2O3 above the temperature. The thermal stability of MnO2 polymorphs is discussed in terms of the bonding environment of oxide ions.
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