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A general chemical transformation route to two-dimensional mesoporous metal selenide nanomaterials by acidification of a ZnSe–amine lamellar hybrid at room temperature

机译:ZnSe-胺层状杂化物在室温下酸化成二维介孔金属硒化物纳米材料的一般化学转化途径

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摘要

Two-dimensional inorganic nanomaterials have drawn much attention due to their excellent properties and wide applications associated with unique 2D structures. However, an efficient and versatile chemical synthesis method using ambient conditions for 2D nanomaterials, especially with secondary structures (e.g. mesopores), has still not been reported. Herein, we report a versatile method to synthesize a family of ultrathin and mesoporous nanosheets of metal selenides based on a precursor so-called “red Se remaining Zn” (RSRZ). The principle of our synthesis is based on a template-assisted chemical transformation process via acidification of inorganic–organic hybrid ZnSe(DETA)0.5 nanosheets (DETA: diethylenetriamine). An appropriate amount of acid was added into an aqueous dispersion of ZnSe(DETA)0.5 nanosheets under air for activation. The acidification induced chemical transformation mechanism was studied by tracking the acidification process. This acid controlled reactivity of lamellar hybrids allows it to be possible to capture the highly reactive intermediates, which will provide a new platform for the synthesis of various mesoporous metal selenides.
机译:二维无机纳米材料因其出色的性能和与独特2D结构相关的广泛应用而备受关注。然而,尚未报道使用环境条件的2D纳米材料,特别是具有二级结构(例如中孔)的有效且通用的化学合成方法。本文中,我们报道了一种基于前体所谓的“剩余红硒”(RSRZ)的金属硒化物超薄和介孔纳米片家族的通用方法。我们的合成原理是基于模板辅助化学转化过程,该过程通过无机-有机杂化ZnSe(DETA)0.5纳米片(DETA:二亚乙基三胺)的酸化而实现。在空气下将适量的酸加入到ZnSe(DETA)0.5纳米片的水分散液中进行活化。通过跟踪酸化过程研究了酸化诱导的化学转化机理。层状杂化物的这种酸控制的反应性使其可以捕获高反应性的中间体,这将为合成各种介孔金属硒化物提供新的平台。

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