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首页> 外文期刊>RSC Advances >Novel hypophosphite hybrid perovskites of [CH3NH2NH2][Mn(H2POO)3] and [CH3NH2NH2][Mn(H2POO)2.83(HCOO)0.17] exhibiting antiferromagnetic order and red photoluminescence
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Novel hypophosphite hybrid perovskites of [CH3NH2NH2][Mn(H2POO)3] and [CH3NH2NH2][Mn(H2POO)2.83(HCOO)0.17] exhibiting antiferromagnetic order and red photoluminescence

机译:[CH3NH2NH2] [Mn(H2POO)3]和[CH 3 N 2] [Mn(H 2 O)2.83(HCOO)0.17]的新型次磷酸盐杂交钙酸盐表现出防铁磁性和红色光致发光

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Hybrid perovskites based on hypophosphite ligands constitute an emerging family of compounds exhibiting unusual structures and offering a platform for construction of novel functional materials. We report the synthesis, crystal structure, and magnetic and optical properties of novel undoped and HCOO ~(?) -doped manganese hypophosphite frameworks templated by methylhydrazinium cations. The undoped compound crystallizes in a three-dimensional perovskite-like orthorhombic structure, space group Pnma , with ordered organic cations located in windows between the perovskite cages expanding along the a -direction. Both conventional anti-phase tilting, unconventional in-phase tilting and columnar shifts in the a -direction are present. Doping with HCOO ~(?) ions has a insignificant influence on the crystal structure but leads to a decrease of the unit cell volume. Magnetic studies indicate that these compounds order antiferromagnetically at T _(N) = 6.5 K. Optical studies indicate that they exhibit red photoluminescence under 266 nm excitation with the activation energy for thermal quenching of 98 and 65 meV for the undoped and doped sample, respectively. For the undoped sample, the emission lifetime reaches 5.05 ms at 77 K but it decreases to 62.26 μs at 300 K. The low value of the activation energy and huge temperature dependence of photoluminescence intensity suggest a high potential of these hypophosphites for non-contact temperature sensing.
机译:基于次磷酸酯配体的杂交钙酸盐构成了一种呈现出不寻常的结构的新兴的化合物,并为建造新型功能材料的平台。我们报告了新型的合成,晶体结构和磁性和光学性质,外布和HCOO〜(α) - 通过甲基腙阳离子模糊的掺杂锰次磷酸酯框架。未掺杂的化合物以三维钙钛矿状的正交结构,空间组PNMA结晶,有有序有机阳离子,位于佩洛夫座架之间的窗户之间沿着-direction扩展。存在常规抗相位倾斜,在-Direction中的非传统的同相倾斜和柱状偏移。掺杂HCOO〜(α)离子对晶体结构的影响微不足道,但导致单元电池体积的降低。磁性研究表明,这些化合物在T _(n)= 6.5k中的反铁磁性顺序。光学研究表明它们在266nm激发下表现出红色光致发光,分别为未掺杂和掺杂样品的热猝灭98和65mev的激活能量。 。对于未掺杂的样品,发射寿命在77 k下达到5.05ms,但它在300k下降至62.26μs。光致发光强度的激活能量和巨大温度依赖性的低值表明这些次磷酸酯的不接触温度传感。

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