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负载单(镍、金)和双金属(镍-金)纳米颗粒的ZnAlO混合氧化物作为用于环境修复的阳光驱动光催化剂

Mono-(Ni, Au) and Bimetallic (Ni-Au) Nanoparticles-Loaded ZnAlO Mixed Oxides as Sunlight-Driven Photocatalysts for Environmental Remediation.

作者信息

Pavel Monica, Cretu Liubovi, Negrila Catalin, Culita Daniela C, Vasile Anca, State Razvan, Balint Ioan, Papa Florica

机构信息

"Ilie Murgulescu" Institute of Physical Chemistry of the Romanian Academy, 202 Spl. Independentei, 060021 Bucharest, Romania.

National Institute of Material Physics, P.O. Box MG 7, 077125 Magurele, Romania.

出版信息

Molecules. 2025 Aug 2;30(15):3249. doi: 10.3390/molecules30153249.

Abstract

A facile and versatile strategy to obtain NPs@ZnAlO nanocomposite materials, comprising controlled-size nanoparticles (NPs) within a ZnAlO matrix is reported. The mono-(Au, Ni) and bimetallic (Ni-Au) NPs serving as an active phase were prepared by the polyol-alkaline method, while the ZnAlO support was obtained via the thermal decomposition of its corresponding layered double hydroxide (LDH) precursors. X-ray diffraction (XRD) patterns confirmed the successful fabrication of the nanocomposites, including the synthesis of the metallic NPs, the formation of LDH-like structure, and the subsequent transformation to ZnO phase upon LDH calcination. The obtained nanostructures confirmed the nanoplate-like morphology inherited from the original LDH precursors, which tended to aggregate after the addition of gold NPs. According to the UV-Vis spectroscopy, loading NPs onto the ZnAlO support enhanced the light absorption and reduced the band gap energy. ATR-DRIFT spectroscopy, H-TPR measurements, and XPS analysis provided information about the functional groups, surface composition, and reducibility of the materials. The catalytic performance of the developed nanostructures was evaluated by the photodegradation of bisphenol A (BPA), under simulated solar irradiation. The conversion of BPA over the bimetallic Ni-Au@ZnAlO reached up to 95% after 180 min of irradiation, exceeding the monometallic Ni@ZnAlO and Au@ZnAlO catalysts. Its enhanced activity was correlated with good dispersion of the bimetals, narrower band gap, and efficient charge carrier separation of the photo-induced e/h pairs.

摘要

报道了一种简便通用的策略来制备NPs@ZnAlO纳米复合材料,该材料在ZnAlO基质中包含尺寸可控的纳米颗粒(NPs)。通过多元醇-碱法制备了作为活性相的单金属(Au、Ni)和双金属(Ni-Au)纳米颗粒,而ZnAlO载体则通过其相应层状双氢氧化物(LDH)前驱体的热分解获得。X射线衍射(XRD)图谱证实了纳米复合材料的成功制备,包括金属纳米颗粒的合成、类LDH结构的形成以及LDH煅烧后向ZnO相的后续转变。所获得的纳米结构证实了继承自原始LDH前驱体的纳米片状形态,在添加金纳米颗粒后这些纳米片趋于聚集。根据紫外-可见光谱,将纳米颗粒负载到ZnAlO载体上增强了光吸收并降低了带隙能量。衰减全反射-漫反射红外傅里叶变换光谱(ATR-DRIFT)、程序升温还原(H-TPR)测量和X射线光电子能谱(XPS)分析提供了有关材料官能团、表面组成和还原性的信息。在模拟太阳辐射下,通过双酚A(BPA)的光降解评估了所开发纳米结构的催化性能。在照射180分钟后,双金属Ni-Au@ZnAlO上BPA的转化率高达95%,超过了单金属Ni@ZnAlO和Au@ZnAlO催化剂。其增强的活性与双金属的良好分散、较窄的带隙以及光生电子/空穴对的有效电荷载流子分离有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37fb/12348654/9af52f8bb77a/molecules-30-03249-g001.jpg

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