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具有二氧化硅层作为矿物氧化还原缓冲层的FeO@SiO@C-Ni杂化物的可控组成和结构

Controllable Compositions and Structures of FeO@SiO@C-Ni Hybrids with a Silica Layer as a Mineral Redox Buffer.

作者信息

Ding Lei, Yang Liting, Xu Jingli, Zheng Jing, Zhang Min

机构信息

College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai 201620, China.

Department of Mechanical, Aerospace & Biomedical Engineering, UT Space Institute, University of Tennessee, Knoxville 37388, Tennessee, United States.

出版信息

Inorg Chem. 2021 Jun 21;60(12):8880-8889. doi: 10.1021/acs.inorgchem.1c00778. Epub 2021 May 27.

DOI:10.1021/acs.inorgchem.1c00778
PMID:34044538
Abstract

Mineral redox buffer is a vital concept in geology that can be applied to modulate hybrid compositions and generate nanostructures with expected morphology. Here, combining a dual coating of an inorganic silica and organic resorcinol-formaldehyde-Ni (RF-Ni) layer on α-FeO spindles with a subsequent calcination process, core-shell FeO@SiO@C-Ni composites with multicompositional structures were fabricated as efficient catalysts for 4-nitrophenol (4-NP) reduction. Notably, the silica layer as a redox buffer between hematite cores and the RF-Ni shell played a crucial role in modulating the compositions and structures of the FeO@SiO@C-Ni. Without the silica layer, FeO-Ni/C composites with Ni nanoparticles trapped into the FeO cores were generated. Moreover, a significant impact of the calcination temperature on morphologies and compositions of the FeO@SiO@C-Ni catalysts along with their catalytic performances has been verified. As a result, the catalyst annealed at 500 °C exhibited a high magnetic property and optimized morphology with high-density small nickel nanoparticles (∼11.6 nm), showing remarkably enhanced catalytic activity compared to the FeO-Ni/C composites and excellent recyclability with a high conservation of about 92%. Furthermore, this synthetic strategy shows significant potential to modulate the nanostructures and phases of other multivalent metal oxide nanocomposites.

摘要

矿物氧化还原缓冲剂是地质学中的一个重要概念,可用于调节混合成分并生成具有预期形态的纳米结构。在此,通过在α-FeO纺锤体上结合无机二氧化硅和有机间苯二酚-甲醛-Ni(RF-Ni)层的双层涂层,并随后进行煅烧过程,制备了具有多组分结构的核壳型FeO@SiO@C-Ni复合材料,作为4-硝基苯酚(4-NP)还原的高效催化剂。值得注意的是,作为赤铁矿核与RF-Ni壳之间的氧化还原缓冲剂的二氧化硅层在调节FeO@SiO@C-Ni的组成和结构方面起着关键作用。没有二氧化硅层时,会生成Ni纳米颗粒被困在FeO核中的FeO-Ni/C复合材料。此外,已证实煅烧温度对FeO@SiO@C-Ni催化剂的形态和组成及其催化性能有显著影响。结果,在500℃退火的催化剂表现出高磁性和优化的形态,具有高密度的小镍纳米颗粒(约11.6nm),与FeO-Ni/C复合材料相比,催化活性显著增强,并且具有约92%的高保留率的优异可回收性。此外,这种合成策略在调节其他多价金属氧化物纳米复合材料的纳米结构和相方面显示出巨大潜力。

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