双氰胺
钙钛矿(结构)
材料科学
猝灭(荧光)
铁电性
离子键合
相(物质)
多铁性
离子电导率
离子
矿物学
化学工程
结晶学
离子液体
化学
电介质
物理化学
光电子学
有机化学
光学
催化作用
物理
电极
电解质
荧光
工程类
作者
Bikash Kumar Shaw,Ashlea R. Hughes,Maxime Ducamp,David A. Keen,François‐Xavier Coudert,Frédéric Blanc,Thomas D. Bennett
标识
DOI:10.26434/chemrxiv.11956599.v1
摘要
Hybrid perovskites occupy a prominent position within solid-state materials chemistry due to their (e.g.) ionic transport, ferroelectric and multiferroic properties. Here we show that a series of [TPrA][M(Dca) 3 ] perovskites (TPrA = tetrapropylammonium cation; Dca = dicyanamide anion; M = Mn, Fe, Co) melt below 300 °C. A combined experimental-computational approach reveal the melting mechanism, and demonstrates that the hybrid perovskites form glasses upon melt quenching which largely retain the inorganic-organic bonding of the crystalline phase. The very low thermal conductivities of these glasses (~ 0.2 W m -1 K -1 ), moderate electrical conductivities (10 -2 – 10 -4 S m -1 ) and thermo-mechanical properties reminiscent of polymeric materials identify them as a new family of functional glass-formers.
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