000 | 03124nlm1a2200457 4500 | ||
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001 | 663392 | ||
005 | 20231030041853.0 | ||
035 | _a(RuTPU)RU\TPU\network\34561 | ||
035 | _aRU\TPU\network\33500 | ||
090 | _a663392 | ||
100 | _a20210209a2019 k y0engy50 ba | ||
101 | 0 | _aeng | |
102 | _aUS | ||
135 | _adrcn ---uucaa | ||
181 | 0 | _ai | |
182 | 0 | _ab | |
200 | 1 |
_aHelicene-SPP-Based Chiral Plasmonic Hybrid Structure: Toward Direct Enantiomers SERS Discrimination _fE. Kalachyova, O. A. Guselnikova, R. Elashnikov [et al.] |
|
203 |
_aText _celectronic |
||
300 | _aTitle screen | ||
330 | _aAchieving chiral plasmon response based on the combination of achiral plasmonic nanostructures with highly chiral surrounding medium represents an attractive way for creation of hybrid optically active plasmonic materials. In this work, we present an attractive design and fabrication of chiral plasmon substrates based on a surface plasmon-polariton-supported structure coupled with extremely optically active helicene enantiomers. Such approach allows us to excite chiral plasmon waves and to design optically active surface-enhanced Raman spectroscopy substrates. Its further combination with standard Raman spectroscopy makes possible enantioselective detection/recognition of optical enantiomers with detection limits below those of standard spectral techniques. The chiral optical response of new plasmonic system was observed and controlled by the optical rotation of helicenes. Without necessity of previous chiral separation or implementation of sophisticated experimental equipment, we were able to estimate the concentration of enantiomers in their mixture by using left- or right-handed chiral plasmon substrates. | ||
333 | _aРежим доступа: по договору с организацией-держателем ресурса | ||
461 | _tACS Applied Materials and Interfaces | ||
463 |
_tVol. 11, iss. 1 _v[P. 1555–1562] _d2019 |
||
610 | 1 | _aэлектронный ресурс | |
610 | 1 | _aтруды учёных ТПУ | |
610 | 1 | _acircular plasmon | |
610 | 1 | _ahelicene | |
610 | 1 | _asurface plasmon-polariton | |
610 | 1 | _achiral SERS | |
610 | 1 | _aenantiomers recognition | |
610 | 1 | _aплазмоны | |
701 | 1 |
_aKalachyova _bE. _cchemical engineer _cassistant of Tomsk Polytechnic University _f1987- _gEvgeniya _2stltpush _3(RuTPU)RU\TPU\pers\39642 |
|
701 | 1 |
_aGuselnikova _bO. A. _cchemist _cengineer of Tomsk Polytechnic University _f1992- _gOlga Andreevna _2stltpush _3(RuTPU)RU\TPU\pers\34478 |
|
701 | 1 |
_aElashnikov _bR. _gRoman |
|
701 | 1 |
_aPanov _bI. _gIllia |
|
701 | 1 |
_aZadny _bJa. _gJaroslav |
|
701 | 1 |
_aCirkva _bV. _gVladimir |
|
712 | 0 | 2 |
_aНациональный исследовательский Томский политехнический университет _bИсследовательская школа химических и биомедицинских технологий _c(2017- ) _h8120 _2stltpush _3(RuTPU)RU\TPU\col\23537 |
801 | 2 |
_aRU _b63413507 _c20210209 _gRCR |
|
856 | 4 | _uhttps://doi.org/10.1021/acsami.8b15520 | |
942 | _cCF |