Modification of Synthetic Valleriite Surface with Gold Nanoparticles: The Roles of Specific Adsorption and Zeta Potential

IF 1.4 4区 化学 Q4 CHEMISTRY, PHYSICAL
A. A. Karacharov, M. N. Likhatski, R. V. Borisov, E. V. Tomashevich, S. A. Vorobyev, S. M. Zharkov
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引用次数: 0

Abstract

Layered two-dimensional materials, whose properties dramatically differ from their bulk precursors, are of great theoretical and applied importance. Recently, a layered 2D material, an analog of a natural mineral, valleriite, in which quasi-monoatomic Cu−Fe−S sheets alternate with brucite-like ones, has been prepared using a simple hydrothermal synthesis procedure. The features of the electronic structure of these materials make it possible to propose them as new materials for a wide field of applications such as (electro)photocatalysis, high-capacity batteries, etc. In this work, nanocomposite materials have been prepared via immobilization of gold nanoparticles (AuNPs) from citrate hydrosols on the surface of the synthesized valleriites having different compositions of hydroxide layers, which control the surface charge density. According to X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), energy-dispersive X-ray microanalysis (EDX), and selected area electron diffraction (SAED) data, AuNPs are immobilized on valleriite nanoflakes, which have lateral sizes of 150–200 nm and thicknesses of several tens of nanometers, as isolated metal nanoparticles with an average diameter of 11 nm. A small amount of aggregates indicates a high affinity of AuNPs for the valleriite surface. The amounts of immobilized gold are the same on all studied valleriites (~0.2%). This finding may be related to the simultaneous sorption of free citrate ions from the AuNP hydrosols, with these ions, according to zeta potential measurements, charging the surfaces of all studied valleriite samples to nearly the same negative value of –40 mV. According to the XPS data, the AuNPs immobilization markedly decreases the magnesium and oxygen contents on the surfaces of the synthesized valleriites due to the partial degradation/dissolution of the brucite layer. In addition, the amount of Fe3+ ions bound to OH groups decreases with a simultaneous increase in the fraction of Fe3+–O species. The TEM data have confirmed the preservation of the layered structure of valleriites after the immobilization of AuNPs.

Abstract Image

用金纳米颗粒修饰合成白云石表面:特定吸附力和 Zeta 电位的作用
摘要层状二维材料的性质与其块体前体有很大不同,具有重要的理论和应用价值。最近,利用一种简单的水热合成方法制备了一种层状二维材料,它是一种天然矿物 valleriite 的类似物,在这种材料中,准原子 Cu-Fe-S 片与类青金石片交替出现。这些材料的电子结构特点使其有可能作为新材料广泛应用于(电)光催化、高容量电池等领域。在这项工作中,通过将柠檬酸盐水溶液中的金纳米颗粒(AuNPs)固定在具有不同氢氧化物层组成的合成瓦勒里石表面,制备了纳米复合材料。根据 X 射线光电子能谱 (XPS)、透射电子显微镜 (TEM)、能量色散 X 射线显微分析 (EDX) 和选区电子衍射 (SAED) 数据,AuNPs 作为平均直径为 11 nm 的孤立金属纳米颗粒固定在侧向尺寸为 150-200 nm、厚度为几十nm 的白云石纳米片上。少量的聚集体表明 AuNPs 与叶绿石表面的亲和力很高。在所有研究的叶绿石上,固定化金的数量相同(约为 0.2%)。这一发现可能与 AuNP 水溶液中同时吸附了游离柠檬酸根离子有关,根据 zeta 电位测量结果,这些离子在所有研究的叶鳞片岩样品表面充电到几乎相同的负值 -40 mV。根据 XPS 数据,由于青金石层的部分降解/溶解,固定 AuNPs 显著降低了合成白云石表面的镁和氧含量。此外,与 OH 基团结合的 Fe3+ 离子数量减少,Fe3+-O 物种的比例也同时增加。TEM 数据证实,在固定 AuNPs 后,白云母的层状结构得以保留。
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来源期刊
Colloid Journal
Colloid Journal 化学-物理化学
CiteScore
2.20
自引率
18.20%
发文量
36
审稿时长
6-12 weeks
期刊介绍: Colloid Journal (Kolloidnyi Zhurnal) is the only journal in Russia that publishes the results of research in the area of chemical science dealing with the disperse state of matter and surface phenomena in disperse systems. The journal covers experimental and theoretical works on a great variety of colloid and surface phenomena: the structure and properties of interfaces; adsorption phenomena and structure of adsorption layers of surfactants; capillary phenomena; wetting films; wetting and spreading; and detergency. The formation of colloid systems, their molecular-kinetic and optical properties, surface forces, interaction of colloidal particles, stabilization, and criteria of stability loss of different disperse systems (lyosols and aerosols, suspensions, emulsions, foams, and micellar systems) are also topics of the journal. Colloid Journal also includes the phenomena of electro- and diffusiophoresis, electro- and thermoosmosis, and capillary and reverse osmosis, i.e., phenomena dealing with the existence of diffusion layers of molecules and ions in the vicinity of the interface.
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