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CaLiPN——一种通过中压合成法制备的四元链状氮磷酸盐。

CaLiPN - A Quaternary Chain-Type Nitridophosphate by Medium-Pressure Synthesis.

作者信息

Pritzl Reinhard M, Fahle Nadine, Witthaut Kristian, Wendl Sebastian, Schnick Wolfgang

机构信息

Department of Chemistry, University of Munich (LMU), Butenandtstraße 5-13, 81377, Munich, Germany.

出版信息

Chemistry. 2024 Sep 16;30(52):e202402521. doi: 10.1002/chem.202402521. Epub 2024 Sep 9.

Abstract

Nitridophosphates are in the focus of current research interest due to their structural versatility and properties, such as ion conductivity, ultra-incompressibility and luminescent properties when doped with suitable activator ions. Multinary representatives often require thorough investigation due to the competition with the thermodynamically more stable binary and ternary compounds. Another point of concern is the synthetic control of structural details, which is usually limited by conventional bottom-up syntheses. In this study, we report on the synthesis and characterization of the quaternary nitridophosphate CaLiPN. Various synthesis protocols were used for the preparation of CaLiPN, including the novel nitridophosphate double salt approach. The crystal structure was solved and refined from single-crystal X-ray diffraction data and confirmed by Rietveld refinement, solid-state NMR spectroscopy, EDX measurements and low-cost crystallographic calculations. The experimental results were corroborated by DFT calculations, which revealed the electronic band structure. Formation energy calculations allowed conclusions to be drawn about the stability in comparison to the initial ternary nitridophosphates. The synthesis of CaLiPN exemplifies the enormous potential of medium-pressure syntheses in the field of nitridophosphate research. Furthermore, the presented new synthesis route allows a certain degree of structural control, which is a promising addition to previous synthesis strategies in nitridophosphate chemistry.

摘要

由于其结构的多样性和诸如离子导电性、超高压缩性以及在掺杂合适的激活离子时的发光特性等性质,氮磷化物成为当前研究的热点。由于与热力学上更稳定的二元和三元化合物存在竞争,多元氮磷化物通常需要深入研究。另一个关注点是结构细节的合成控制,这通常受到传统自下而上合成方法的限制。在本研究中,我们报道了四元氮磷化物CaLiPN的合成与表征。我们使用了各种合成方案来制备CaLiPN,包括新颖的氮磷化物复盐法。通过单晶X射线衍射数据解析并精修了晶体结构,并通过Rietveld精修、固态核磁共振光谱、能谱分析和低成本晶体学计算进行了确认。密度泛函理论(DFT)计算证实了实验结果,揭示了电子能带结构。通过形成能计算,可以得出与初始三元氮磷化物相比的稳定性结论。CaLiPN的合成例证了中压合成在氮磷化物研究领域的巨大潜力。此外,所提出的新合成路线允许一定程度的结构控制,这是对先前氮磷化物化学合成策略的一个有前景的补充。

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