氢通量合成锰(V)氧化物结晶:各向异性生长和电化学稳定性的控制

David, Portehault, Carlos V. M., Inocêncio, Almudena, Torres-Pardo, David, Montero, Lucien, Roach, Pierre-Olivier, Autran, Capucine, Sassoye, Cyril, Aymonier, Aurea, Varela, Marina, Parras, Christel, Laberty-Robert
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摘要

尽管具有有趣的光学、磁性和氧化还原特性,但含有五价锰(Mn5+)的无机材料非常罕见,并且永远无法被设计为形状控制晶体,这限制了调整性能的能力。在此,我们探索了具有控制含水量的氢氧化碱混合物,即流体通量,以展示Mn(V)氧化物的相,形状和纳米结构控制。我们证明了KSrMnVO4、Sr5(MnVO4)3OH和SrMnIVO3的形态与氢氧化盐的含水量、锶含量和碱阳离子的性质有关。然后,我们提供了水在实现形状和纳米结构控制中的关键作用的证据,我们将其与水与羟基磷灰石Sr5(MnVO4)3OH的特定晶体面的优先相互作用以及水对前驱体在缺水流体中的溶解度的影响联系起来。然后,我们证明纳米结构的Mn(V)羟基磷灰石具有酸碱氧化还原稳定性窗口,能够在强氧化条件下进行电化学操作。通过将流体助熔剂的基本知识与结晶机制相关联,这项工作揭示了流体助熔剂为晶体形状、大小和性质控制提供的可能性。
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Crystallization of manganese (V) oxides by hydroflux synthesis: Control of anisotropic growth and electrochemical stability
Despite intriguing optical, magnetic, and redox properties, inorganic materials containing pentavalent manganese (Mn5+) are rare and could never be designed as shape-controlled crystals, which limits the ability to tune properties. Herein, we explore alkali hydroxide mixtures with controlled water content, namely hydrofluxes, to demonstrate phase, shape, and nanostructure control of Mn(V) oxides. We demonstrate speciation among KSrMnVO4, Sr5(MnVO4)3OH, and SrMnIVO3 with the water content, the strontium content, and the nature of the alkali cation of the hydroxide salt. We then provide evidence of the key role of water in enabling shape and nanostructure control, which we relate to the preferential interaction of water with specific crystal facets of the hydroxyapatite Sr5(MnVO4)3OH, and to the impact of water on precursor solubility in water-poor hydrofluxes. We then show that nanostructured Mn(V) hydroxyapatite possesses an acid-base redox stability window enabling electrochemical operation in strongly oxidative conditions. By correlating fundamental knowledge of hydrofluxes with crystallization mechanisms, this work sheds light on the possibilities offered by hydrofluxes for crystal shape, size and property control.
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