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新型次磷酸盐杂化钙钛矿[CHNHNH][Mn(HPOO)]和[CHNHNH][Mn(HPOO)(HCOO)]呈现反铁磁有序和红色光致发光。

Novel hypophosphite hybrid perovskites of [CHNHNH][Mn(HPOO)] and [CHNHNH][Mn(HPOO)(HCOO)] exhibiting antiferromagnetic order and red photoluminescence.

作者信息

Mączka Mirosław, Gągor Anna, Pikul Adam, Stefańska Dagmara

机构信息

Institute of Low Temperature and Structure Research, Polish Academy of Sciences Box 1410 50-950 Wrocław 2 Poland

出版信息

RSC Adv. 2020 May 19;10(32):19020-19026. doi: 10.1039/d0ra03397a. eCollection 2020 May 14.

DOI:10.1039/d0ra03397a
PMID:35518310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9053939/
Abstract

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 , with ordered organic cations located in windows between the perovskite cages expanding along the -direction. Both conventional anti-phase tilting, unconventional in-phase tilting and columnar shifts in the -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 = 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.

摘要

基于次磷酸盐配体的杂化钙钛矿构成了一类新兴的化合物家族,它们具有独特的结构,并为新型功能材料的构建提供了一个平台。我们报道了由甲基肼鎓阳离子模板化的新型未掺杂和甲酸掺杂的次磷酸锰骨架的合成、晶体结构以及磁学和光学性质。未掺杂的化合物结晶为三维钙钛矿状正交结构,空间群为 ,有序的有机阳离子位于沿 方向扩展的钙钛矿笼之间的窗口中。同时存在传统的反相倾斜、非传统的同相倾斜以及沿 方向的柱状位移。用甲酸根离子掺杂对晶体结构影响不大,但导致晶胞体积减小。磁性研究表明,这些化合物在 = 6.5 K 时呈反铁磁有序。光学研究表明,它们在 266 nm 激发下呈现红色光致发光,未掺杂和掺杂样品的热猝灭激活能分别为 98 和 65 meV。对于未掺杂样品 在 77 K 时发射寿命达到 5.05 ms,但在 300 K 时降至 62.26 μs。激活能的低值和光致发光强度对温度的巨大依赖性表明这些次磷酸盐在非接触温度传感方面具有很高的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850e/9053939/37105f2969a3/d0ra03397a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850e/9053939/7fbfb6eab391/d0ra03397a-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850e/9053939/37105f2969a3/d0ra03397a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850e/9053939/7fbfb6eab391/d0ra03397a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850e/9053939/8c94be48f6c6/d0ra03397a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850e/9053939/4f02469d03d9/d0ra03397a-f3.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850e/9053939/a80c4deae076/d0ra03397a-f5.jpg
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本文引用的文献

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