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Multiferroic Core-Shell Nanofibers, Assembly in a Magnetic Field, and Studies on Magneto-Electric Interactions.多铁性核壳纳米纤维、在磁场中的组装以及磁电相互作用研究
Materials (Basel). 2017 Dec 23;11(1):18. doi: 10.3390/ma11010018.
2
DNA as a powerful tool for morphology control, spatial positioning, and dynamic assembly of nanoparticles.DNA作为控制纳米颗粒形态、空间定位和动态组装的强大工具。
Acc Chem Res. 2014 Jun 17;47(6):1881-90. doi: 10.1021/ar500081k. Epub 2014 May 28.
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Strategies for optimizing DNA hybridization on surfaces.优化表面DNA杂交的策略。
Anal Biochem. 2014 Jan 1;444:41-6. doi: 10.1016/j.ab.2013.09.032. Epub 2013 Oct 9.
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An exceptionally simple strategy for DNA-functionalized up-conversion nanoparticles as biocompatible agents for nanoassembly, DNA delivery, and imaging.一种非常简单的策略,用于将 DNA 功能化的上转换纳米粒子作为用于纳米组装、DNA 传递和成像的生物相容试剂。
J Am Chem Soc. 2013 Feb 20;135(7):2411-4. doi: 10.1021/ja310432u. Epub 2013 Feb 7.
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Tuning and assembling metal nanostructures with DNA.利用 DNA 对金属纳米结构进行调谐和组装。
Chem Commun (Camb). 2013 Apr 4;49(26):2597-609. doi: 10.1039/c2cc37536b.
6
Probing the local strain-mediated magnetoelectric coupling in multiferroic nanocomposites by magnetic field-assisted piezoresponse force microscopy.磁场辅助压电力显微镜研究多铁性纳米复合材料中局域应变介导的磁电耦合。
Nanoscale. 2012 May 21;4(10):3218-27. doi: 10.1039/c2nr00064d. Epub 2012 Apr 20.
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Ordered arrays of multiferroic epitaxial nanostructures.多铁性外延纳米结构的有序阵列
Nano Rev. 2011;2. doi: 10.3402/nano.v2i0.7364. Epub 2011 Oct 4.
8
Recent progress in multiferroic magnetoelectric composites: from bulk to thin films.多铁性磁电复合材料的最新进展:从体相到薄膜。
Adv Mater. 2011 Mar 4;23(9):1062-87. doi: 10.1002/adma.201003636. Epub 2011 Feb 4.
9
Magnetoelectric coupling effects in multiferroic complex oxide composite structures.多铁复合氧化物复合材料中的磁电耦合效应。
Adv Mater. 2010 Jul 20;22(26-27):2900-18. doi: 10.1002/adma.200904326.
10
Polyvalent oligonucleotide iron oxide nanoparticle "click" conjugates.多价寡核苷酸氧化铁纳米粒子“点击”偶联物。
Nano Lett. 2010 Apr 14;10(4):1477-80. doi: 10.1021/nl100477m.

使用DNA功能化纳米粒子的多铁性核壳复合材料的自组装。

Self-assembly of multiferroic core-shell composites using DNA functionalized nanoparticles.

作者信息

Banerjee Atanu, Zhang Jitao, Zhou Peng, Tuppil Koushik, Sreenivasulu Gollapudi, Qu Hongwei, Zhang Tianjin, Timilsina Roshan, Chavez Ferman A, Srinivasan Gopalan

机构信息

Department of Chemistry, Oakland University, Rochester, MI 48309-4401, United States.

Department of Physics, Oakland University, Rochester, MI 48309-4401, United States.

出版信息

J Magn Magn Mater. 2018 Aug 15;460:424-431. doi: 10.1016/j.jmmm.2018.03.075. Epub 2018 Apr 4.

DOI:10.1016/j.jmmm.2018.03.075
PMID:33981128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8112619/
Abstract

Ferrite-ferroelectric core-shell nanoparticles were prepared by deoxyribonucleic acid (DNA) assisted self-assembly and the strained mediated magneto-electric (ME) interactions between the ferroic phases were studied. The nanoparticle type and size were varied and the DNA linker sequence was also varied. Two kinds of particles, one with 600 nm barium titanate (BTO) core and 200 nm nickel ferrite (NFO) shell and another with 200 nm BTO core and 50 nm nickel cobalt ferrite (NCFO) shell were prepared. The particles were linked by three different oligomeric DNA containing 19, 18 or 30 base pairs. The core-shell structure was evident from electron microscopy and scanning microwave microscopy images. Films and disks of the core-shell particles were assembled in a magnetic field and used for measurements of low frequency ME voltage coefficient (MEVC) and magnet-dielectric effect. The MEVC data on films indicate that particles assembled with DNA with 30 base pairs exhibit the strongest ME coupling suggesting a more fully integrated heterogenous nanocomposite and the weakest interaction for DNA with 18 base pairs. These results indicate that the longer linker region in DNA is the key factor for forming better composites. This result may be due to the irregular shape of the nanoparticles. Longer DNA strands would be able to bridge better generating more linkages. Shorter strands would not able to bridge the irregularly shaped particles as well and therefore result in linkages and less heterogeneity in the composites.

摘要

通过脱氧核糖核酸(DNA)辅助自组装制备了铁氧体-铁电核壳纳米颗粒,并研究了铁电相之间的应变介导磁电(ME)相互作用。改变了纳米颗粒的类型和尺寸,也改变了DNA连接子序列。制备了两种颗粒,一种是具有600 nm钛酸钡(BTO)核和200 nm镍铁氧体(NFO)壳的颗粒,另一种是具有200 nm BTO核和50 nm镍钴铁氧体(NCFO)壳的颗粒。这些颗粒通过三种不同的含有19、18或30个碱基对的寡聚DNA连接。核壳结构在电子显微镜和扫描微波显微镜图像中很明显。核壳颗粒的薄膜和圆盘在磁场中组装,并用于测量低频ME电压系数(MEVC)和磁介电效应。薄膜的MEVC数据表明,用30个碱基对的DNA组装的颗粒表现出最强的ME耦合,表明形成了更完全整合的异质纳米复合材料,而用18个碱基对的DNA表现出最弱的相互作用。这些结果表明,DNA中较长的连接区域是形成更好复合材料的关键因素。这一结果可能是由于纳米颗粒的不规则形状。较长的DNA链能够更好地桥接,产生更多的连接。较短的链则不能很好地桥接不规则形状的颗粒,因此导致连接减少,复合材料中的异质性降低。

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