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首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Porous Two-Dimensional Nanosheets Converted from Layered Double Hydroxides and Their Applications in Electrocatalytic Water Splitting
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Porous Two-Dimensional Nanosheets Converted from Layered Double Hydroxides and Their Applications in Electrocatalytic Water Splitting

机译:层状双氢氧化物转化的多孔二维纳米片及其在电催化水分解中的应用

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Porous materials are of particular interest due to their high surface area and rich edge sites, which are favorable for applications such as catalysis. Although there are well-established strategies for synthesizing porous metal oxides (e.g., by annealing the corresponding metal hydroxides), facile and scalable routes to porous metal hydroxides and metal chalcogenides are lacking. Here, we report a simple and general strategy to synthesize porous nanosheets of metal hydroxides by selectively etching layered double hydroxide (LDH) nanoplate precursors that contain amphoteric metal and to further convert them into porous metal chalcogenides by a solution method. Using NiGa LDH as an example, we show that the thin nanoplates with high surface accessibility facilitate the topotactic conversion of NiGa LDH to beta-Ni(OH), and further to NiSe, with porous texture while preserving the sheet-like morphology. The converted beta-Ni(OH), and NiSe2 are highly active for electrocatalytic oxygen evolution reaction and hydrogen evolution reaction (HER), respectively, which demonstrates the applications of such high surface area porous nanostructures with rich edge sites. Particularly, the porous NiSe2 nanosheets exhibited excellent catalytic activity toward HER with low onset overpotential, small Tafel slope, and good stability under both acidic and alkaline conditions. Overall electrochemical water splitting experiments using these porous beta-Ni(OH)(2) and NiSe, nanosheets were further demonstrated. Our work presents a new strategy to prepare porous nanomaterials and to further enhance their catalytic and other applications.
机译:多孔材料由于其高的表面积和丰富的边缘位置而特别受到关注,这对于诸如催化的应用是有利的。尽管已经有成熟的合成多孔金属氧化物的策略(例如,通过退火相应的金属氢氧化物),但是仍然缺乏到多孔金属氢氧化物和金属硫属化物的简便且可扩展的途径。在这里,我们报告了一种简单而通用的策略,即通过选择性蚀刻包含两性金属的层状双氢氧化物(LDH)纳米板前体,然后通过溶液法将其进一步转化为多孔金属硫属元素化物,来合成金属氢氧化物的多孔纳米片。以NiGa LDH为例,我们表明具有高表面可及性的薄纳米板有助于NiGa LDH的全向立构转化为β-Ni(OH),并进一步转化为NiSe,具有多孔结构,同时保留了片状形态。转化的β-Ni(OH)和NiSe2分别对电催化的析氧反应和析氢反应(HER)具有高活性,这证明了这种具有高边缘位点的高表面积多孔纳米结构的应用。特别地,多孔NiSe 2纳米片对HER表现出优异的催化活性,具有低的起始过电势,小的Tafel斜率以及在酸性和碱性条件下的良好稳定性。进一步证明了使用这些多孔β-Ni(OH)(2)和NiSe纳米片的整体电化学水分解实验。我们的工作提出了一种制备多孔纳米材料并进一步增强其催化和其他应用的新策略。

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