In-plane anisotropic Raman response of layered In2Te5 semiconductor

2021 ◽  
Vol 118 (18) ◽  
pp. 182105
Author(s):  
Yulan Zhou ◽  
Weike Wang ◽  
Liang Li ◽  
Penglai Gong ◽  
Dongsheng Tang
Keyword(s):  
Author(s):  
Alexander Konetschny ◽  
Marcel Weinhold ◽  
Christian Heiliger ◽  
Matthias Thomas Elm ◽  
Peter J. Klar

Square-shaped Ce0.8Gd0.2O2 (GDC) membranes are prepared by microstructuring techniques from (111)-oriented, polycrystalline GDC thin films. The strain state of the membranes is investigated by micro-Raman mapping using polarized excitation light....


2006 ◽  
Vol 26 (14) ◽  
pp. 2855-2859 ◽  
Author(s):  
Jan Petzelt ◽  
Tetyana Ostapchuk ◽  
Ivan Gregora ◽  
Maxim Savinov ◽  
Dagmar Chvostova ◽  
...  

2015 ◽  
Vol 54 (6) ◽  
pp. 219-224 ◽  
Author(s):  
Elena Buixaderas ◽  
Christelle Kadlec ◽  
Premysl Vaněk ◽  
Silvo Drnovšek ◽  
Hana Uršič ◽  
...  

2013 ◽  
Vol 536 ◽  
pp. 142-146 ◽  
Author(s):  
C. Camerlingo ◽  
M.P. Lisitskiy ◽  
L. De Stefano ◽  
I. Rea ◽  
I. Delfino ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2181
Author(s):  
Ryan D. Mellor ◽  
Andreas G. Schätzlein ◽  
Ijeoma F. Uchegbu

Gold nanoparticles (AuNPs) are used experimentally for non-invasive in vivo Raman monitoring because they show a strong absorbance in the phototherapeutic window (650–850 nm), a feature that is accompanied by a particle size in excess of 100 nm. However, these AuNPs cannot be used clinically because they are likely to persist in mammalian systems and resist excretion. In this work, clustered ultrasmall (sub-5 nm) AuNP constructs for in vivo Raman diagnostic monitoring, which are also suitable for mammalian excretion, were synthesized and characterized. Sub-5 nm octadecyl amine (ODA)-coated AuNPs were clustered using a labile dithiol linker: ethylene glycol bis-mercaptoacetate (EGBMA). Upon clustering via a controlled reaction and finally coating with a polymeric amphiphile, a strong absorbance in the phototherapeutic window was demonstrated, thus showing the potential suitability of the construct for non-invasive in vivo detection and monitoring. The clusters, when labelled with a biphenyl-4-thiol (BPT) Raman tag, were shown to elicit a specific Raman response in plasma and to disaggregate back to sub-5 nm particles under physiological conditions (37 °C, 0.8 mM glutathione, pH 7.4). These data demonstrate the potential of these new AuNP clusters (Raman NanoTheranostics—RaNT) for in vivo applications while being in the excretable size window.


2001 ◽  
Vol 64 (18) ◽  
Author(s):  
J. Petzelt ◽  
T. Ostapchuk ◽  
I. Gregora ◽  
I. Rychetský ◽  
S. Hoffmann-Eifert ◽  
...  

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Yoad Michael ◽  
Leon Bello ◽  
Michael Rosenbluh ◽  
Avi Pe’er

Abstract The sensitivity of classical Raman spectroscopy methods, such as coherent anti-stokes Raman spectroscopy (CARS) or stimulated Raman spectroscopy (SRS), is ultimately limited by shot-noise from the stimulating fields. We present the complete theoretical analysis of a squeezing-enhanced version of Raman spectroscopy that overcomes the shot-noise limit of sensitivity with enhancement of the Raman signal and inherent background suppression, while remaining fully compatible with standard Raman spectroscopy methods. By incorporating the Raman sample between two phase-sensitive parametric amplifiers that squeeze the light along orthogonal quadrature axes, the typical intensity measurement of the Raman response is converted into a quantum-limited, super-sensitive estimation of phase. The resonant Raman response in the sample induces a phase shift to signal-idler frequency-pairs within the fingerprint spectrum of the molecule, resulting in amplification of the resonant Raman signal by the squeezing factor of the parametric amplifiers, whereas the non-resonant background is annihilated by destructive interference. Seeding the interferometer with classical coherent light stimulates the Raman signal further without increasing the background, effectively forming squeezing-enhanced versions of CARS and SRS, where the quantum enhancement is achieved on top of the classical stimulation.


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