Sergey Novikov

Dr. Sergey Novikov

Centre of Advanced Studies, Moscow, Moskva, Russia
orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
20 June 2012 in Nano Letters
Verified
Journal Article
Closed access
Andrey B. EvlyukhinAndrey B. Evlyukhin
Andrey B. Evlyukhin
SNSergey Novikov
Sergey Novikov
UZUrs Zywietz
Urs Zywietz
RERené Eriksen
René Eriksen
CRCarsten Reinhardt
Carsten Reinhardt
Boris ChichkovBoris Chichkov
Boris Chichkov

8 February 2021 in Nature Communications
Verified
Journal Article
Open access
PDF file
GEGeorgy Ermolaev
Georgy Ermolaev
DGDmitriy Grudinin
Dmitriy Grudinin
YSY. V. Stebunov
Y. V. Stebunov
KVKirill Voronin
Kirill Voronin
VKV. G. Kravets
V. G. Kravets
Valentyn S. VolkovValentyn S. Volkov
Valentyn S. Volkov
Large optical anisotropy observed in a broad spectral range is of paramount importance for efficient light manipulation in countless devices. Although a giant anisotropy has been recently observed in the mid-infrared wavelength range, for visible and near-infrared spectral intervals, the problem remains acute with the highest reported birefringence values of 0.8 in BaTiS3 and h-BN crystals. This issue inspired an intensive search for giant optical anisotropy among natural and artificial materials. Here, we demonstrate that layered transition metal dichalcogenides (TMDCs) provide an answer to this quest owing to their fundamental differences between intralayer strong covalent bonding and weak interlayer van der Waals interaction. To do this, we made correlative far- and near-field characterizations validated by first-principle calculations that reveal a huge birefringence of 1.5 in the infrared and 3 in the visible light for MoS2. Our findings demonstrate that this remarkable anisotropy allows for tackling the diffraction limit enabling an avenue for on-chip next-generation photonics.

1 January 2012 in Nature Communications
Verified
Journal Article
Open access
PDF file
TSThomas Søndergaard
Thomas Søndergaard
SNSergey Novikov
Sergey Novikov
THTobias Holmgaard
Tobias Holmgaard
RERené Eriksen
René Eriksen
JBJonas Beermann
Jonas Beermann
SBSergey Bozhevolnyi
Sergey Bozhevolnyi
Excitation of localized and delocalized surface plasmon resonances can be used for turning excellent reflectors of visible light, such as gold and silver, into efficient absorbers, whose wavelength, polarization or angular bandwidths are however necessarily limited owing to the resonant nature of surface plasmon excitations involved. Nonresonant absorption has so far been achieved by using combined nano- and micro-structural surface modifications and with composite materials involving metal nanoparticles embedded in dielectric layers. Here we realize nonresonant light absorption in a well-defined geometry by using ultra-sharp convex metal grooves via adiabatic nanofocusing of gap surface plasmon modes excited by scattering off subwavelength-sized wedges. We demonstrate experimentally that two-dimensional arrays of sharp convex grooves in gold ensure efficient (>87%) broadband (450–850 nm) absorption of unpolarized light, reaching an average level of 96%. Efficient absorption of visible light by nanostructured metal surfaces open new exciting perspectives within plasmonics, especially for thermophotovoltaics.

10 July 2020 in npj 2D Materials and Applications
Verified
Journal Article
Open access
PDF file
GEGeorgy Ermolaev
Georgy Ermolaev
YSYury V. Stebunov
Yury V. Stebunov
AVAndrey A. Vyshnevyy
Andrey A. Vyshnevyy
DTDmitriy Tatarkin
Dmitriy Tatarkin
DYDmitry Yakubovsky
Dmitry Yakubovsky
VVValentyn S. Volkov
Valentyn S. Volkov
Layered semiconductors such as transition metal dichalcogenides (TMDs) offer endless possibilities for designing modern photonic and optoelectronic components. However, their optical engineering is still a challenging task owing to multiple obstacles, including the absence of a rapid, contactless, and the reliable method to obtain their dielectric function as well as to evaluate in situ the changes in optical constants and exciton binding energies. Here, we present an advanced approach based on ellipsometry measurements for retrieval of dielectric functions and the excitonic properties of both monolayer and bulk TMDs. Using this method, we conduct a detailed study of monolayer MoS2 and its bulk crystal in the broad spectral range (290–3300 nm). In the near- and mid-infrared ranges, both configurations appear to have no optical absorption and possess an extremely high dielectric permittivity making them favorable for lossless subwavelength photonics. In addition, the proposed approach opens a possibility to observe a previously unreported peak in the dielectric function of monolayer MoS2 induced by the use of perylene-3,4,9,10-tetracarboxylic acid tetrapotassium salt (PTAS) seeding promoters for MoS2 synthesis and thus enables its applications in chemical and biological sensing. Therefore, this technique as a whole offers a state-of-the-art metrological tool for next-generation TMD-based devices.

24 July 2015 in Nanotechnology
Verified
Journal Article
Closed access
JLJudith Langer
Judith Langer
SNSergey Novikov
Sergey Novikov
LLLuis M Liz-Marzán
Luis M Liz-Marzán
Nanoparticles are widely used in various fields of science and technology as well as in everyday life. In particular, gold and silver nanoparticles display unique optical properties that render them extremely attractive for various applications. In this review, we focus on the use of noble metal nanoparticles as plasmonic nanosensors with extremely high sensitivity, even reaching single molecule detection. Sensors based on plasmon resonance shifts, as well as the use of surface-enhanced Raman scattering and surface-enhanced fluorescence, will be considered in this work.

2 May 2014 in Small
Verified
Journal Article
Closed access
PDF file
LPLakshminarayana Polavarapu
Lakshminarayana Polavarapu
APAndrea La Porta
Andrea La Porta
SNSergey Novikov
Sergey Novikov
MCMarc Coronado‐Puchau
Marc Coronado‐Puchau
LLLuis M. Liz‐Marzán
Luis M. Liz‐Marzán