Self‐Assembly of Biocompatible FeSe Hollow Nanostructures and 2D CuFeSe Nanosheets with One‐ and Two‐Photon Luminescence Properties

Small ◽  
2019 ◽  
Vol 15 (31) ◽  
pp. 1900627 ◽  
Author(s):  
Yang Deng ◽  
Dianqi Li ◽  
Xingming Ning ◽  
Dongxu Zhang ◽  
Shouting Zhang ◽  
...  
2013 ◽  
Vol 19 (34) ◽  
pp. 11279-11286 ◽  
Author(s):  
Shu-Ran Zhang ◽  
Dong-Ying Du ◽  
Ke Tan ◽  
Jun-Sheng Qin ◽  
Hui-Qing Dong ◽  
...  

2010 ◽  
Vol 114 (17) ◽  
pp. 8084-8088 ◽  
Author(s):  
Xiao Ming Yin ◽  
Cheng Chao Li ◽  
Ming Zhang ◽  
Quan Yi Hao ◽  
Shuang Liu ◽  
...  

2015 ◽  
Vol 185 ◽  
pp. 249-266 ◽  
Author(s):  
Christopher M. Lemon ◽  
Daniel G. Nocera

Whereas a variety of covalent conjugation strategies have been utilized to prepare quantum dot (QD)-based nanosensors, supramolecular approaches of self-assembly have been underexplored. A major advantage of self-assembly is the ability to circumvent laborious synthetic efforts attendant to covalent conjugation of a chemosensor to functionalized QDs. Here, we combine a CdSe/ZnS core–shell QD with gold(iii) corroles using both self-assembly and micelle encapsulation to form QD nanosensors. Appreciable spectral overlap between QD emission and corrole absorption results in efficient Förster resonance energy transfer (FRET), which may be initiated by one- or two-photon excitation. The triplet state of the gold(iii) corroles is quenched by molecular oxygen, enabling these constructs to function as optical O2 sensors, which is useful for the metabolic profiling of tumours. The photophysical properties, including QD and corrole lifetimes, FRET efficiency, and O2 sensitivity, have been determined for each construct. The relative merits of each conjugation strategy are assessed with regard to their implementation as sensors.


1983 ◽  
Vol 93 (1) ◽  
pp. 89-96 ◽  
Author(s):  
C. Linares ◽  
P. Jung ◽  
G. Boulon ◽  
F. Gaume

2017 ◽  
Vol 49 ◽  
pp. 85-97
Author(s):  
Bo Pang ◽  
Xiang Xi Meng ◽  
Yang Long Hou ◽  
Hong Fang Sun ◽  
Qiu Shi Ren

The synthesis of anisotropic branched gold nanoparticles remines to be challenging as their arm number and arm length could hardly be controlled, greatly limited their biomedical application. We report the large-scale high-yield synthesis of PdCu@Au tripods, and, for the first time, their two-photon luminescence properties with quantitative characterization of the two-photon action cross section as well as quantum yield. By introducing nitrogen protection to the synthesis of the PdCu bimetallic cores, this approach eliminates the oxidative etching caused by oxygen in the air, providing a 2.5 times higher synthetic yield of 70.4 %, which enables the large-scale preparation of PdCu@Au at ca. 380 mg per batch. By the conformal coating of PdCu bimetallic cores, the PdCu@Au tripods are prepared with a purity of >90 % with average arm length 45.3 ± 5.6 nm that is ideal for biomedical applications. The PdCu@Au tripods demonstrate a much brighter two-photon luminescence than that from Au nanorods, with a 3.6 ± 0.9 times larger two-photon action cross section and comparable quantum yield. Our result also shows the two-photon luminescence property of PdCu@Au tripods could be tuned by their distinct localized surface plasmon resonance property and, in turn, the different amount of Au coating. This tunability could be explained by the recently-proposed two-step excitation mechanism of two-photon luminescence in Au nanoparticle. The folate-targeted in vitro two-photon luminescence imaging of MDA-MB-435 breast cancer cells were also demonstrated to show the great potential using PdCu@Au tripods as novel multi-functional platforms for cancer theranostics.


2015 ◽  
Vol 112 (15) ◽  
pp. 4546-4551 ◽  
Author(s):  
Angel Martinez ◽  
Leonardo Hermosillo ◽  
Mykola Tasinkevych ◽  
Ivan I. Smalyukh

Geometric shape and topology of constituent particles can alter many colloidal properties such as Brownian motion, self-assembly, and phase behavior. Thus far, only single-component building blocks of colloids with connected surfaces have been studied, although topological colloids, with constituent particles shaped as freestanding knots and handlebodies of different genus, have been recently introduced. Here we develop a topological class of colloids shaped as multicomponent links. Using two-photon photopolymerization, we fabricate colloidal microparticle analogs of the classic examples of links studied in the field of topology, the Hopf and Solomon links, which we disperse in nematic fluids that possess orientational ordering of anisotropic rod-like molecules. The surfaces of these particles are treated to impose tangential or perpendicular boundary conditions for the alignment of liquid crystal molecules, so that they generate a host of topologically nontrivial field and defect structures in the dispersing nematic medium, resulting in an elastic coupling between the linked constituents. The interplay between the topologies of surfaces of linked colloids and the molecular alignment field of the nematic host reveals that linking of particle rings with perpendicular boundary conditions is commonly accompanied by linking of closed singular defect loops, laying the foundations for fabricating complex composite materials with interlinking-based structural organization.


2021 ◽  
Vol 18 (10) ◽  
pp. 106003
Author(s):  
Jun Dai ◽  
Zhengguo Li ◽  
Yi Zhang ◽  
Yongzhu Chen ◽  
Xing Zhu ◽  
...  

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