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Photochemical Synthesis and Catalytic Applicationsof Gold Nanoplates Fabricated Using Quercetin Diphosphate Macromolecules

机译:光化学合成及催化应用槲皮素二磷酸大分子制备金纳米板的制备

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摘要

The demand for safer design and synthesis of gold nanoparticles (AuNPs) is on the increase with the ultimate goal of producing clean nanomaterials for biological applications. We hereby present a rapid, greener, and photochemical synthesis of gold nanoplates with sizes ranging from 10 to 200 nm using water-soluble quercetin diphosphate (QDP) macromolecules. The synthesis was achieved in water without the use of surfactants, reducing agents, or polymers. The edge length of the triangular nanoplates ranged from 50 to 1200 nm. Furthermore, the reduction of methylene blue was used to investigate the catalytic activity of AuNPs. The catalytic activity of triangular AuNPs was three times higher than that of the spherical AuNPs based on kinetic rate constants (k). The rate constants were 3.44 × 10–2 and 1.11 × 10–2 s–1 for triangular and spherical AuNPs, respectively. The X-ray diffraction data of gold nanoplates synthesized by this method exhibited that the nanocrystals were mainly dominated by (111) facets which are in agreement to the nanoplates synthesized by usingthermal and chemical approaches. The calculated relative diffractionpeak intensity of (200), (220), and (311) in comparison with (111)was found to be 0.35, 0.17, and 0.15, respectively, which were lowerthan the corresponding standard values (JCPDS 04-0784). For example,(200)/(111) = 0.35 compared to 0.52 obtained from the standard (JCPDS04-0784), indicating that the gold nanoplates are dominated by (111)facets. The calculated lattice from selected area electron diffractiondata of the as-synthesized and after 1 year nanoplates was 4.060 and4.088 Å, respectively. Our calculations were found to be in agreementwith 4.078 Å for face-centered cubic gold (JCPDS 04-0784) andliterature values of 4.07 Å. The computed QDP–Au complexdemonstrated that the reduction process took place in the B ring ofQDP. This approach contributes immensely to promoting the ideals ofsustainable nanotechnology by eradicating the use of hazardous andtoxic organic solvents.
机译:对安全设计和合成金纳米颗粒(AuNPs)的需求正在增长,其最终目标是生产用于生物应用的清洁纳米材料。我们在此提出使用水溶性槲皮素二磷酸(QDP)大分子快速,更绿色和光化学合成尺寸从10到200 nm的金纳米板。合成是在水中完成的,无需使用表面活性剂,还原剂或聚合物。三角形纳米板的边缘长度范围为50至1200 nm。此外,亚甲基蓝的还原被用来研究AuNPs的催化活性。基于动力学速率常数(k),三角形AuNPs的催化活性是球形AuNPs的三倍。三角形和球形AuNP的速率常数分别为3.44×10 –2 和1.11×10 –2 s -1 。通过该方法合成的金纳米板的X射线衍射数据表明,纳米晶体主要由(111)面支配,这与通过使用该方法合成的纳米板一致。热化学方法。计算的相对衍射与(111)相比(200),(220)和(311)的峰值强度被发现分别为0.35、0.17和0.15,这是较低的比相应的标准值(JCPDS 04-0784)高。例如,(200)/(111)= 0.35,而从标准(JCPDS04-0784),表明金纳米板主要由(111)方面。根据选定区域电子衍射计算出的晶格合成后和1年后纳米板的数据为4.060和分别为4.088Å。我们的计算结果是一致的具有4.078Å的面心立方金(JCPDS 04-0784)和文献值为4.07Å。计算的QDP–Au复数证明还原过程发生在B环QDP。这种方法极大地促进了人们的理想通过消除有害和有害物质的使用来实现可持续的纳米技术有毒的有机溶剂。

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