Evidence of the Core–Shell Structure of (Photo)magnetic CoFe Prussian Blue Analogue Nanoparticles and Peculiar Behavior of the Surface Species

2018 ◽  
Vol 140 (32) ◽  
pp. 10332-10343 ◽  
Author(s):  
Amélie Bordage ◽  
Robinson Moulin ◽  
Emiliano Fonda ◽  
Giulia Fornasieri ◽  
Eric Rivière ◽  
...  
Keyword(s):  
Prussian Blue ◽  
Shell Structure ◽  
Core Shell ◽  
Surface Species ◽  
Prussian Blue Analogue ◽  
The Core ◽  
Core Shell Structure ◽  
Peculiar Behavior

scholarly journals A SERS Study of Charge Transfer Process in Au Nanorod–MBA@Cu2O Assemblies: Effect of Length to Diameter Ratio of Au Nanorods

Nanomaterials ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 867
Author(s):  
Lin Guo ◽  
Zhu Mao ◽  
Sila Jin ◽  
Lin Zhu ◽  
Junqi Zhao ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Shell Structure ◽  
Shell Structures ◽  
Core Shell ◽  
Absorption Bands ◽  
Au Nanorods ◽  
The Core ◽  
Band Position ◽  
Surface Enhanced Raman ◽  
Core Shell Structure

Surface-enhanced Raman scattering (SERS) is a powerful tool in charge transfer (CT) process research. By analyzing the relative intensity of the characteristic bands in the bridging molecules, one can obtain detailed information about the CT between two materials. Herein, we synthesized a series of Au nanorods (NRs) with different length-to-diameter ratios (L/Ds) and used these Au NRs to prepare a series of core–shell structures with the same Cu2O thicknesses to form Au NR–4-mercaptobenzoic acid (MBA)@Cu2O core–shell structures. Surface plasmon resonance (SPR) absorption bands were adjusted by tuning the L/Ds of Au NR cores in these assemblies. SERS spectra of the core-shell structure were obtained under 633 and 785 nm laser excitations, and on the basis of the differences in the relative band strengths of these SERS spectra detected with the as-synthesized assemblies, we calculated the CT degree of the core–shell structure. We explored whether the Cu2O conduction band and valence band position and the SPR absorption band position together affect the CT process in the core–shell structure. In this work, we found that the specific surface area of the Au NRs could influence the CT process in Au NR–MBA@Cu2O core–shell structures, which has rarely been discussed before.

Construction of MOFs-Shell Porous Materials and Performance Study in Selective Adsorption and Separation of Benzene Pollutants

2021 ◽  
Author(s):  
Yu Qiao ◽  
Na Lv ◽  
Dong Li ◽  
Hongji Li ◽  
Xiangxin Xue ◽  
...  
Keyword(s):  
Porous Materials ◽  
Shell Structure ◽  
Selective Adsorption ◽  
Core Shell ◽  
Architecture Design ◽  
Performance Study ◽  
The Core ◽  
Core Shell Structure ◽  
And Performance ◽  
Sacrificial Agent

Metastable Cu2O is an attractive material for the architecture design of integrated nanomaterials. In this context, Cu2O was used as the sacrificial agent to form the core-shell structure of Cu2O@HKUST-1...

Preparation of polyacrylamide microspheres with core–shell structure via surface-initiated atom transfer radical polymerization

RSC Advances ◽  
2016 ◽  
Vol 6 (94) ◽  
pp. 91463-91467 ◽  
Author(s):  
Peng Zhang ◽  
Shixun Bai ◽  
Shilan Chen ◽  
Dandan Li ◽  
Zhenfu Jia ◽  
...  
Keyword(s):  
Atom Transfer Radical Polymerization ◽  
Radical Polymerization ◽  
Shell Structure ◽  
Core Shell ◽  
Atom Transfer ◽  
The Core ◽  
Core Shell Structure

Well defined core–shell microspheres were prepared by surface-initiated atom transfer radical polymerization with pre-crosslinked polyacrylamide as the core and non-crosslinked polyacrylamide as the shell.

Core–shell stability of nanoparticles plays an important role for overcoming the intestinal mucus and epithelium barrier

2016 ◽  
Vol 4 (35) ◽  
pp. 5831-5841 ◽  
Author(s):  
Min Liu ◽  
Lei Wu ◽  
Xi Zhu ◽  
Wei Shan ◽  
Lian Li ◽  
...  
Keyword(s):  
Shell Structure ◽  
Core Shell ◽  
The Core ◽  
Shell Stability ◽  
Intestinal Mucus ◽  
Core Shell Structure ◽  
The Stability

The stability of the core–shell structure plays an important role in the nanoparticles ability to overcome both the mucus and epithelium absorption barrier.

Characterization of Fe3O4@CS@NMDP magnetic nanoparticles with core–shell structure prepared by chemical cross-linking method

2017 ◽  
Vol 10 (05) ◽  
pp. 1750056 ◽  
Author(s):  
Huiping Shao ◽  
Jiangcong Qi ◽  
Tao Lin ◽  
Yuling Zhou ◽  
Fucheng Yu
Keyword(s):  
Magnetic Nanoparticles ◽  
Shell Structure ◽  
High Performance ◽  
Cross Linking ◽  
Composite Particles ◽  
Core Shell ◽  
The Core ◽  
Targeting Delivery ◽  
Core Shell Structure ◽  
Chemical Cross Linking

The core–shell structure composite magnetic nanoparticles (NPs), Fe3O4@chitosan@nimodipine (Fe3O4@CS@NMDP), were successfully synthesized by a chemical cross-linking method in this paper. NMDP is widely used for cardiovascular and cerebrovascular disease prevention and treatment, while CS is of biocompatibility. The composite particles were characterized by an X-ray diffractometer (XRD), a Fourier transform infrared spectroscopy (FT-IR), a transmission electron microscopy (TEM), a vibrating sample magnetometers (VSM) and a high performance liquid chromatography (HPLC). The results show that the size of the core–shell structure composite particles is ranging from 12[Formula: see text]nm to 20[Formula: see text]nm and the coating thickness of NMDP is about 2[Formula: see text]nm. The saturation magnetization of core–shell composite NPs is 46.7[Formula: see text]emu/g, which indicates a good potential application for treating cancer by magnetic target delivery. The release percentage of the NMDP can reach 57.6% in a short time of 20[Formula: see text]min in the PBS, and to 100% in a time of 60[Formula: see text]min, which indicates the availability of Fe3O4@CS@NMDP composite NPs for targeting delivery treatment.

The use of galvanic displacement in synthesizing Pt(Cu) catalysts with the core-shell structure

2010 ◽  
Vol 46 (10) ◽  
pp. 1189-1197 ◽  
Author(s):  
B. I. Podlovchenko ◽  
T. D. Gladysheva ◽  
A. Yu. Filatov ◽  
L. V. Yashina
Keyword(s):  
Shell Structure ◽  
Core Shell ◽  
Galvanic Displacement ◽  
The Core ◽  
Cu Catalysts ◽  
Core Shell Structure

Seed-mediated synthesis of bimetallic ruthenium–platinum nanoparticles efficient in cinnamaldehyde selective hydrogenation

2014 ◽  
Vol 43 (24) ◽  
pp. 9283-9295 ◽  
Author(s):  
Xueqiang Qi ◽  
M. Rosa Axet ◽  
Karine Philippot ◽  
Pierre Lecante ◽  
Philippe Serp
Keyword(s):  
Selective Hydrogenation ◽  
Platinum Nanoparticles ◽  
Shell Structure ◽  
Core Shell ◽  
The Core ◽  
Core Shell Structure ◽  
Seed Mediated

The two-step synthesis of small ruthenium–platinum nanoparticles leads to the formation of a core–shell structure. The catalytic results provide supplementary evidence of the core–shell structure.

A cosolvency effect on tunable thermosensitive core–shell nanoparticle gels

Soft Matter ◽  
2015 ◽  
Vol 11 (19) ◽  
pp. 3936-3945 ◽  
Author(s):  
Sang Min Lee ◽  
Young Chan Bae
Keyword(s):  
Transition Temperature ◽  
Shell Structure ◽  
Core Shell ◽  
The Core ◽  
Volume Transition ◽  
Core Shell Structure ◽  
Propanol Solution

Schematic depiction of a core–shell structure composed of the PMMA core and the PHEMA shell, and the influence of three co-solvents on the volume transition temperature of the core–shell gels in 1-propanol solution.

Design of PP/EPDM/NBR TPVs with tunable mechanical properties via regulating the core-shell structure

2020 ◽  
Vol 90 ◽  
pp. 106767
Author(s):  
Tao Peng ◽  
Fei Lv ◽  
Zhou Gong ◽  
Liming Cao ◽  
Xuesong Yan ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Shell Structure ◽  
Core Shell ◽  
The Core ◽  
Core Shell Structure ◽  
Tunable Mechanical Properties

Strain engineering of metal-based nanomaterials for energy electrocatalysis

2019 ◽  
Vol 48 (12) ◽  
pp. 3265-3278 ◽  
Author(s):  
Zhonghong Xia ◽  
Shaojun Guo
Keyword(s):  
Solid Solution ◽  
Shell Structure ◽  
Strain Engineering ◽  
Solid Solution Alloy ◽  
Core Shell ◽  
The Core ◽  
Multiple Defects ◽  
Recent Advances ◽  
Core Shell Structure ◽  
Induced Structure

This work presents recent advances in strain engineering via the core–shell structure, solid solution alloy and multiple defects-induced structure.

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