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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[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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摘要

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 mu s 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。我们报道了由甲基腙阳离子模板模板模板的新型未掺杂和HCOO - 掺杂的锰次磷酸酯框架的合成,晶体结构和磁性和光学性质。未掺杂的化合物在三维钙钛矿状正交结构中结晶,空间组PNMA,位于沿着方向扩展的钙钛矿笼之间的有序有机阳离子。存在常规抗相位倾斜,在方向上存在非传统的相倾斜和柱状偏移。用HCOOION掺杂对晶体结构具有微不足道的影响,但导致单位细胞体积的降低。磁性研究表明,这些化合物在T-N = 6.5k处偏析反铁磁性。光学研究表明它们在266nm激发下表现出红色光致发光,其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,排放寿命在77 k下达到5.05毫秒,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较高潜力温度传感。

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  • 来源
    《RSC Advances》 |2020年第32期|共7页
  • 作者单位

    Polish Acad Sci Inst Low Temp &

    Struct Res Box 1410 PL-50950 Wroclaw 2 Poland;

    Polish Acad Sci Inst Low Temp &

    Struct Res Box 1410 PL-50950 Wroclaw 2 Poland;

    Polish Acad Sci Inst Low Temp &

    Struct Res Box 1410 PL-50950 Wroclaw 2 Poland;

    Polish Acad Sci Inst Low Temp &

    Struct Res Box 1410 PL-50950 Wroclaw 2 Poland;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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