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Author	Kirilenko, D.A.; Brunkov, P.N.
Title	Measuring the height-to-height correlation function of corrugation in suspended graphene			Type	A1 Journal article
Year	2016	Publication	Ultramicroscopy	Abbreviated Journal	Ultramicroscopy
Volume	165	Issue	165	Pages	1-7
Keywords	A1 Journal article; Electron Microscopy for Materials Science (EMAT);
Abstract	Nanocorrugation of 2D crystals is an important phenomenon since it affects their electronic and mechanical properties. The corrugation may have various sources; one of them is flexural phonons that, in particular, are responsible for the thermal conductivity of graphene. A study of corrugation of just the suspended graphene can reveal much of valuable information on the physics of this complicated phenomenon. At the same time, the suspended crystal nanorelief can hardly be measured directly because of high flexibility of the 2D crystal. Moreover, the relief portion related to rapid out-of-plane oscillations (flexural phonons) is also inaccessible by such measurements. Here we present a technique for measuring the Fourier components of the height-height correlation function H(q) of suspended graphene which includes the effect of flexural phonons. The technique is based on the analysis of electron diffraction patterns. The H(q) is measured in the range of wavevectors q approximately 0.4-4.5nm(-1). At the upper limit of this range H(q) does follow the T/kappaq(4) law. So, we measured the value of suspended graphene bending rigidity kappa=1.2+/-0.4eV at ambient temperature T approximately 300K. At intermediate wave vectors, H(q) follows a slightly weaker exponent than theoretically predicted q(-3.15) but is closer to the results of the molecular dynamics simulation. At low wave vectors, the dependence becomes even weaker, which may be a sign of influence of charge carriers on the dynamics of undulations longer than 10nm. The technique presented can be used for studying physics of flexural phonons in other 2D materials.
Address	Ioffe Institute, Politekhnicheskaya ul. 26, 194021 St-Petersburg, Russia; ITMO University, Kronverksky pr. 49, 197101 St. Petersburg, Russia
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language	English	Wos	000375946200001	Publication Date	2016-03-28
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0304-3991	ISBN		Additional Links
Impact Factor	2.843	Times cited	3	Open Access
Notes	D.K. thanks the RFBR (Grant no. 16-32-60165) for the partial support of this research. The work was carried out in part at the Joint Research Center “Material Science and Characterization in Advanced Technologies” (St-Petersburg, Russia) under the financial support from the Ministry of Education and Science of the Russian Federation (Agreement 14.621.21.0007, 04.12.2014, id RFMEFI62114X0007, the use of the Jeol JEM-2100F microscope) and at EMAT, Universiteit Antwerpen (Antwerpen, Belgium), (the use of the FEI Tecnai G2 microscope).			Approved	Most recent IF: 2.843
Call Number	EMAT @ emat @			Serial	4124
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Author	Kirilenko, D.A.; Dideykin, A.T.; Aleksenskiy, A.E.; Sitnikova, A.A.; Konnikov, S.G.; Vul', A.Y.
Title	One-step synthesis of a suspended ultrathin graphene oxide film: Application in transmission electron microscopy			Type	A1 Journal article
Year	2015	Publication	Micron	Abbreviated Journal	Micron
Volume	68	Issue	68	Pages	23-26
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Ultrathin graphene films find their use as advantageous support for nano- and biomaterials investigations. Thin film causes a very slight deterioration to measured signals, thus providing more details of the object's structure at nanoscale. The ultimate thinness of graphene works in the best way for this purpose. However, obtaining suspended thin film of a large-area, which is convenient for applications, is often a relatively complicated and time-consuming task. Here we present a one-step 1-min technique for synthesis of an extremely thin (about 1-2 nm) continuous film suspended over cells of a conventional copper grid (50-400 mu m mesh). This technique enables us to acquire a large-area film which is water-resistant, stable in organic solvents and can act as a support when studying nanoparticles or biomaterials. Moreover, the very mechanism of the film formation can be interesting from the point of view of other applications of ultrathin graphene oxide papers. (C) 2014 Elsevier Ltd. All rights reserved.
Address
Corporate Author				Thesis
Publisher		Place of Publication	Oxford	Editor
Language		Wos	000348016500004	Publication Date	2014-08-30
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0968-4328;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	1.98	Times cited	13	Open Access
Notes				Approved	Most recent IF: 1.98; 2015 IF: 1.988
Call Number	c:irua:123800			Serial	2467
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Author	Kirilenko, D.A.
Title	Electron diffraction measurement of the binding rigidity of free-standing graphene			Type	A1 Journal article
Year	2013	Publication	Technical physics letters	Abbreviated Journal	Tech Phys Lett+
Volume	39	Issue	4	Pages	325-328
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	A method for measuring the binding rigidity of free-standing graphene from the dependence of the short-wavelength spectral range of transverse structural fluctuations of a crystal is proposed. The fluctuation spectrum is measured according to the variation in electron-diffraction patterns derived in a transmission electron microscope while tilting the sample.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000319162600003	Publication Date	2013-05-16
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	1063-7850;1090-6533;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	0.771	Times cited	3	Open Access
Notes				Approved	Most recent IF: 0.771; 2013 IF: 0.583
Call Number	UA @ lucian @ c:irua:109031			Serial	920
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Author	Trofimova, E.Y.; Kurdyukov, D.A.; Yakovlev, S.A.; Kirilenko, D.A.; Kukushkina, Y.A.; Nashchekin, A.V.; Sitnikova, A.A.; Yagovkina, M.A.; Golubev, V.G.
Title	Monodisperse spherical mesoporous silica particles : fast synthesis procedure and fabrication of photonic-crystal films			Type	A1 Journal article
Year	2013	Publication	Nanotechnology	Abbreviated Journal	Nanotechnology
Volume	24	Issue	15	Pages	155601-155611
Keywords	A1 Journal article; Engineering sciences. Technology; Electron microscopy for materials research (EMAT)
Abstract	A procedure for the synthesis of monodisperse spherical mesoporous silica particles (MSMSPs) via the controlled coagulation of silica/surfactant clusters into spherical aggregates with mean diameters of 250-1500 nm has been developed. The synthesis is fast (taking less than 1 h) because identical clusters are simultaneously formed in the reaction mixture. The results of microscopic, x-ray diffraction, adsorption and optical measurements allowed us to conclude that the clusters are similar to 15 nm in size and have hexagonally packed cylindrical pore channels. The channel diameters in MSMSPs obtained with cethyltrimethylammonium bromide and decyltrimethylammonium bromide as structure-directing agents were 3.1 +/- 0.15 and 2.3 +/- 0.12 nm, respectively. The specific surface area and the pore volume of MSMSP were, depending on synthesis conditions, 480-1095 m(2) g(-1) and 0.50-0.65 cm(3) g(-1). The MSMSP were used to grow opal-like photonic-crystal films possessing a hierarchical macro-mesoporous structure, with pores within and between the particles. A selective filling of mesopore channels with glycerol, based on the difference between the capillary pressures in macro- and mesopores, was demonstrated. It is shown that this approach makes it possible to control the photonic bandgap position in mesoporous opal films by varying the degree of mesopore filling with glycerol. Online supplementary data available from stacks.iop.org/Nano/24/155601/mmedia
Address
Corporate Author				Thesis
Publisher		Place of Publication	Bristol	Editor
Language		Wos	000316988700009	Publication Date	2013-03-22
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0957-4484;1361-6528;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.44	Times cited	49	Open Access
Notes				Approved	Most recent IF: 3.44; 2013 IF: 3.672
Call Number	UA @ lucian @ c:irua:108462			Serial	2191
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Author	Kuznetsov, A.S.; Lu, Y.-G.; Turner, S.; Shestakov, M.V.; Tikhomirov, V.K.; Kirilenko, D.; Verbeeck, J.; Baranov, A.N.; Moshchalkov, V.V.
Title	Preparation, structural and optical characterization of nanocrystalline ZnO doped with luminescent Ag-nanoclusters			Type	A1 Journal article
Year	2012	Publication	Optical materials express	Abbreviated Journal	Opt Mater Express
Volume	2	Issue	6	Pages	723-734
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Nanocrystalline ZnO doped with Ag-nanoclusters has been synthesized by a salt solid state reaction. Three overlapping broad emission bands due to the Ag nanoclusters have been detected at about 570, 750 and 900 nm. These emission bands are excited by an energy transfer from the exciton state of the ZnO host when pumped in the wavelength range from 250 to 400 nm. The 900 nm emission band shows characteristic orbital splitting into three components pointing out that the anisotropic crystalline wurtzite host of ZnO is responsible for this feature. Heat-treatment and temperature dependence studies confirm the origin of these emission bands. An energy level diagram for the emission process and a model for Ag nanoclusters sites are suggested. The emission of nanocrystalline ZnO doped with Ag nanoclusters may be applied for white light generation, displays driven by UV light, down-convertors for solar cells and luminescent lamps.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000304953700004	Publication Date	2012-04-30
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	2159-3930;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	2.591	Times cited		Open Access
Notes	We are grateful to the Methusalem Funding of Flemish Government for the support of this work. Y.-G. L. and S. T. acknowledge funding from the Fund for Scientific Research Flanders (FWO) for a postdoctoral grant and under grant number G056810N. The microscope used in this study was partially financed by the Hercules Foundation. J.V. acknowledges funding from the European Research Council under the 7th Framework Program (FP7), ERC grant No246791 – COUNTATOMS and ERC Starting Grant 278510 VORTEX. The authors acknowledge the guidance of Prof. G. Van Tendeloo, EMAT Antwerpen University, in transmission electron microscopy study in this work. ECASJO_;			Approved	Most recent IF: 2.591; 2012 IF: 2.616
Call Number	UA @ lucian @ c:irua:97709UA @ admin @ c:irua:97709			Serial	2707
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Author	Tikhomirov, V.K.; Rodríguez, V.D.; Méndez-Ramos, J.; del- Castillo, J.; Kirilenko, D.; Van Tendeloo, G.; Moshchalkov, V.V.
Title	Optimizing Er/Yb ratio and content in Er-Yb co-doped glass-ceramics for enhancement of the up- and down-conversion luminescence			Type	A1 Journal article
Year	2012	Publication	Solar energy materials and solar cells	Abbreviated Journal	Sol Energ Mat Sol C
Volume	100	Issue		Pages	209-215
Keywords	A1 Journal article; Engineering sciences. Technology; Electron microscopy for materials research (EMAT)
Abstract	Er3+Yb3+ co-doped transparent glass-ceramics with varying Er/Yb content and ratio have been prepared. High quantum yields for up- and down-conversion luminescence by energy transfer from Yb3+ to Er3+ and from Er3+ to Yb3+, respectively, have been detected and optimized with respect to the Er/Yb content and ratio, and proposed in particular for up- and down-conversion of solar spectrum for enhancement of the efficiency of solar cells. The rise and decay kinetics for the population of the excited levels of Er3+ and Yb3+ have been studied and fit. Based on these experimental data, the mechanisms for the energy transfers have been suggested with emphasis on the optimized Er/Yb content and ratio for enhancement of the efficiency of the Er3+↔Yb3+ energy transfers.
Address
Corporate Author				Thesis
Publisher		Place of Publication	Amsterdam	Editor
Language		Wos	000303034700030	Publication Date	2012-02-04
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0927-0248;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	4.784	Times cited	66	Open Access
Notes	Fwo			Approved	Most recent IF: 4.784; 2012 IF: 4.630
Call Number	UA @ lucian @ c:irua:97392			Serial	2493
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Author	Tikhomirov, V.K.; Vosch, T.; Fron, E.; Rodríguez, V.D.; Velázquez, J.J.; Kirilenko, D.; Van Tendeloo, G.; Hofkens, J.; Van der Auweraer, M.; Moshchalkov, V.V.
Title	Luminescence of oxyfluoride glasses co-doped with Ag nanoclusters and Yb³⁺ ions			Type	A1 Journal article
Year	2012	Publication	RSC advances	Abbreviated Journal	Rsc Adv
Volume	2	Issue	4	Pages	1496-1501
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Bulk oxyfluoride glasses co-doped with Ag nanoclusters and Yb3+ ions have been prepared by a melt quenching technique. When excited in the absorption band of the Ag nanoclusters between 300 to 500 nm, these glasses emit a broad band characteristic of the Ag nanoclusters between 400 to 750 nm as well as an emission band between 900 to 1100 nm, originating from Yb3+ ions. The intensity ratio of the Yb3+/Ag emission bands increases with the Ag doping level at a fixed concentration of Yb3+, indicating the presence of energy transfer mechanism from the Ag nanoclusters to the Yb3+ ions. Comparison of time-resolved decay kinetics of the luminescence in the respectively Ag nanocluster-Yb3+ co-doped and single Ag nanocluster doped glasses, hints towards an energy transfer from the red and infrared emitting Ag nanoclusters to the Yb3+ ions.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000299695300038	Publication Date	2011-12-19
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	2046-2069;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.108	Times cited	46	Open Access
Notes	Fwo; Iap			Approved	Most recent IF: 3.108; 2012 IF: 2.562
Call Number	UA @ lucian @ c:irua:96239			Serial	1856
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Author	Kuznetsov, A.S.; Cuong, N.T.; Tikhomirov, V.K.; Jivanescu, M.; Stesmans, A.; Chibotaru, L.F.; Velázquez, J.J.; Rodríguez, V.D.; Kirilenko, D.; Van Tendeloo, G.; Moshchalkov, V.V.
Title	Effect of heat-treatment on luminescence and structure of Ag nanoclusters doped oxyfluoride glasses and implication for fiber drawing			Type	A1 Journal article
Year	2012	Publication	Optical materials	Abbreviated Journal	Opt Mater
Volume	34	Issue	4	Pages	616-621
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	The effect of heat treatment on the structure and luminescence of Ag nanoclusters doped oxyfluoride glasses was studied and the implication for drawing the corresponding fibers doped with luminescent Ag nanoclusters has been proposed. The heat treatment results, first, in condensation of the Ag nanoclusters into larger Ag nanoparticles and loss of Ag luminescence, and further heat treatment results in precipitation of a luminescent-loss nano- and microcrystalline Ag phases onto the surface of the glass. Thus, the oxyfluoride fiber doped with luminescent Ag nanoclusters was pulled from the viscous glass melt and its attenuation loss was 0.19 dB/cm in the red part of the spectrum; i.e. near to the maximum of Ag nanoclusters luminescence band. The nucleation centers for the Ag nanoclusters in oxyfluoride glasses have been suggested to be the fluorine vacancies and their nanoclusters.
Address
Corporate Author				Thesis
Publisher		Place of Publication	Amsterdam	Editor
Language		Wos	000300124500006	Publication Date	2011-10-18
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0925-3467;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	2.238	Times cited	25	Open Access
Notes	Methusalem			Approved	Most recent IF: 2.238; 2012 IF: 1.918
Call Number	UA @ lucian @ c:irua:93632			Serial	811
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Author	Kirilenko, D.
Title	Characterization of graphene by electron diffraction			Type	Doctoral thesis
Year	2012	Publication		Abbreviated Journal
Volume		Issue		Pages
Keywords	Doctoral thesis; Electron microscopy for materials research (EMAT)
Abstract
Address
Corporate Author				Thesis
Publisher		Place of Publication	Antwerpen	Editor
Language		Wos		Publication Date	0000-00-00
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN		ISBN		Additional Links	UA library record
Impact Factor		Times cited		Open Access
Notes				Approved	Most recent IF: NA
Call Number	UA @ lucian @ c:irua:98834			Serial	323
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Author	Kirilenko, D.A.; Dideykin, A.T.; Van Tendeloo, G.
Title	Measuring the corrugation amplitude of suspended and supported graphene			Type	A1 Journal article
Year	2011	Publication	Physical review : B : condensed matter and materials physics	Abbreviated Journal	Phys Rev B
Volume	84	Issue	23	Pages	235417-235417,5
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Nanoscale corrugation is a fundamental property of graphene arising from its low-dimensional nature. It places a fundamental limit to the conductivity of graphene and influences its properties. However the degree of the influence of the corrugation has not been well established because of the little knowledge about its spectrum in suspended graphene. We present a transmission electron microscopy technique that enables us to measure the average corrugation height and length. We applied the technique also to measure the temperature dependence of the corrugation. The difference in corrugation between suspended and supported graphene has been illustrated.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000297764700003	Publication Date	2011-12-03
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	1098-0121;1550-235X;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.836	Times cited	31	Open Access
Notes				Approved	Most recent IF: 3.836; 2011 IF: 3.691
Call Number	UA @ lucian @ c:irua:93629			Serial	1971
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Author	Shestakov, M.V.; Tikhomirov, V.K.; Kirilenko, D.; Kuznetsov, A.S.; Chibotaru, L.F.; Baranov, A.N.; Van Tendeloo, G.; Moshchalkov, V.V.
Title	Quantum cutting in Li (770 nm) and Yb (1000 nm) co-dopant emission bands by energy transfer from the ZnO nano-crystalline host			Type	A1 Journal article
Year	2011	Publication	Optics express	Abbreviated Journal	Opt Express
Volume	19	Issue	17	Pages	15955-15964
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Li-Yb co-doped nano-crystalline ZnO has been synthesized by a method of thermal growth from the salt mixtures. X-ray diffraction, transmission electron microscopy, atomic absorption spectroscopy and optical spectroscopy confirm the doping and indicate that the dopants may form Li-Li and Yb3+-Li based nanoclusters. When pumped into the conduction and exciton absorption bands of ZnO between 250 to 425 nm, broad emission bands of about 100 nm half-height-width are excited around 770 and 1000 nm, due to Li and Yb dopants, respectively. These emission bands are activated by energy transfer from the ZnO host mostly by quantum cutting processes, which generate pairs of quanta in Li (770 nm) and Yb (1000 nm) emission bands, respectively, out of one quantum absorbed by the ZnO host. These quantum cutting phenomena have great potential for application in the down-conversion layers coupled to the Si solar cells.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000293894900033	Publication Date	2011-08-04
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	1094-4087;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.307	Times cited	19	Open Access
Notes	FWO; Methusalem			Approved	Most recent IF: 3.307; 2011 IF: 3.587
Call Number	UA @ lucian @ c:irua:92428			Serial	2776
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Author	Hezareh, T.; Razavi, F.S.; Kremer, R.K.; Habermeier, H.-U.; Lebedev, O.I.; Kirilenko, D.; Van Tendeloo, G.
Title	Effect of PbZr_0.52Ti_0.48O₃ thin layer on structure, electronic and magnetic properties of La_0.65Sr_0.35MnO₃ and La_0.65Ca_0.30MnO₃ thin-films			Type	A1 Journal article
Year	2011	Publication	Journal of applied physics	Abbreviated Journal	J Appl Phys
Volume	109	Issue	11	Pages	113707,1-113707,8
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Epitaxial thin film heterostructures of high dielectric PbZr<sub>1-x</sub>Ti<sub>x</sub>O<sub>3</sub> (PZT) and La<sub>1-x</sub>A<sub>x</sub>MnO<sub>3</sub> (A-divalent alkaline earth metals such as Sr (LSMO) and Ca (LCMO)) were grown on SrTiO<sub>3</sub> substrates and their structure, temperature dependence of electrical resistivity, and magnetization were investigated as a function of the thickness of the LSMO(LCMO) layer. The microstructures of the samples were analyzed by TEM. By applying an electric field across the PZT layer, we applied a ferrodistortive pressure on the manganite layer and studied the correlations between lattice distortion and electric transport and magnetic properties of the CMR materials.
Address
Corporate Author				Thesis
Publisher	American Institute of Physics	Place of Publication	New York, N.Y.	Editor
Language		Wos	000292214700069	Publication Date	2011-06-06
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0021-8979;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	2.068	Times cited	4	Open Access
Notes				Approved	Most recent IF: 2.068; 2011 IF: 2.168
Call Number	UA @ lucian @ c:irua:90964			Serial	843
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Author	Lin, H.; Ohta, T.; Paul, A.; Hutchison, J.A.; Kirilenko, D.; Lebedev, O.; Van Tendeloo, G.; Hofkens, J.; Uji-i, H.
Title	Light-assisted nucleation of silver nanowires during polyol synthesis			Type	A1 Journal article
Year	2011	Publication	Journal of photochemistry and photobiology: A: chemistry	Abbreviated Journal	J Photoch Photobio A
Volume	221	Issue	2/3	Pages	220-223
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	This report describes the effect of light irradiation on the synthesis of silver nanowires by the well-known polyol method. High quality nanowires are produced in high yields when the reaction suspension is irradiated with 400500 nm light during the nucleation stage. These studies suggest that light accelerates the formation of the nanoparticle seeds most appropriate for nanowire growth.
Address
Corporate Author				Thesis
Publisher		Place of Publication	Lausanne	Editor
Language		Wos	000293813800018	Publication Date	2011-04-19
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	1010-6030;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	2.625	Times cited	24	Open Access
Notes	Fwo; Iap			Approved	Most recent IF: 2.625; 2011 IF: 2.421
Call Number	UA @ lucian @ c:irua:91262			Serial	1818
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Author	Razdobarin, A.G.; Mukhin, E.E.; Semenov, V.V.; Tolstyakov, S.Y.; Kochergin, M.M.; Kurskiev, G.S.; Podushnikova, K.A.; Kirilenko, D.A.; Sitnikova, A.A.; Konovalov, V.G.; Solodovchenko, S.I.; Nekhaieva, O.M.; Skorik, O.A.; Bondarenko, V.N.; Voitsenya, V.S.;
Title	Diagnostic mirrors with transparent protection layer for ITER			Type	A1 Journal article
Year	2011	Publication	Fusion engineering and design	Abbreviated Journal	Fusion Eng Des
Volume	86	Issue	6-8	Pages	1341-1344
Keywords	A1 Journal article; Engineering sciences. Technology; Electron microscopy for materials research (EMAT)
Abstract	Fast degradation of in-vessel optics is one of the most serious problems for all optical diagnostics in ITER. To provide the resistance to mechanical and thermal stresses along with a high stability of optical characteristics under deposition-dominated conditions we suggest using high-reflective metallic (Ag or Al) film mirrors coated on silicon substrate and protected with thin oxide film in the divertor Thomson Scattering (TS) diagnostics. The mirrors coated with Al2O3 and ZrO2 films were tested under irradiation by deuterium ions. The experimental results on the oxide films sputtering are discussed in the context of their applicability for the first mirror protection in ITER.
Address
Corporate Author				Thesis
Publisher	Elsevier science sa	Place of Publication	Amsterdam	Editor
Language		Wos	000297426500203	Publication Date	2011-03-17
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0920-3796;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	1.319	Times cited	6	Open Access
Notes				Approved	Most recent IF: 1.319; 2011 IF: 1.490
Call Number	UA @ lucian @ c:irua:93631			Serial	686
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Author	Dideykin, A.; Aleksenskiy, A.E.; Kirilenko, D.; Brunkov, P.; Goncharov, V.; Baidakova, M.; Sakseev, D.; Vul', A.Y.
Title	Monolayer graphene from graphite oxide			Type	A1 Journal article
Year	2011	Publication	Diamond and related materials	Abbreviated Journal	Diam Relat Mater
Volume	20	Issue	2	Pages	105-108
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Graphene, a new carbon material, is attracting presently an increasing research interest. It stems from the unique electrical and mechanical properties of graphene predicted by theory. Experimental studies of graphene are, however, severely curtailed by a lack of an appropriate technique for its preparation. Mechanical cleavage of graphite proved to be ineffective, since it yields only very small (a few microns in size) particles of monolayer graphene. The rapidly developing approach based on chemical exfoliation of graphite produces large-area coatings composed primarily of arbitrarily oriented multilayer graphene particles. We have developed a technique for preparation of monolayer graphene sheets involving liquid exfoliation of crystalline graphite, which includes synthesis of graphite oxide by deep oxidation as an intermediate stage. Electron diffraction traces, as well as the variation of diffracted intensities with local orientation of graphene sheets, AFM, and HRTEM images testify to a remarkably good monolayer structure of the graphite oxide particles obtained by our technique. These results open a way to setting up high-efficiency production of monolayer graphene sheets appropriate for electrical and optical measurements and fabrication of structures for use in the field of applications.
Address
Corporate Author				Thesis
Publisher		Place of Publication	Amsterdam	Editor
Language		Wos	000288145500010	Publication Date	2010-10-31
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0925-9635;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	2.561	Times cited	48	Open Access
Notes				Approved	Most recent IF: 2.561; 2011 IF: 1.913
Call Number	UA @ lucian @ c:irua:88791			Serial	2193
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Author	Tikhomirov, V.K.; Rodriguez, V.D.; Kutznetsov, D.; Kirilenko, D.; Van Tendeloo, G.; Moshchalkov, V.V.
Title	Preparation and luminescence of bulk oxyfluoride glasses doped with Ag nanoclusters			Type	A1 Journal article
Year	2010	Publication	Optics express	Abbreviated Journal	Opt Express
Volume	18	Issue	21	Pages	22032-22040
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Bulk oxyfluoride glasses doped with Ag nanoclusters have been prepared using the melt quenching technique. When pumped in the absorption band of Ag nanoclusters between 300 to 500 nm, these glasses emit a very broad luminescence band covering all the visible range with a weak tail extending into the near infrared. The maximum of the luminescence band and its color shifts to the blue with a shortening of the excitation wavelength and an increasing ratio of oxide to fluoride components, resulting in white color luminescence at a particular ratio of oxide to fluoride; with a quantum yield above 20%.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000283686500057	Publication Date	2010-10-04
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	1094-4087;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.307	Times cited	74	Open Access
Notes	Methusalem			Approved	Most recent IF: 3.307; 2010 IF: 3.753
Call Number	UA @ lucian @ c:irua:85802			Serial	2698
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Author	van den Heuvel, W.; Tikhomirov, V.K.; Kirilenko, D.; Schildermans, N.; Chibotaru, L.F.; Vanacken, J.; Gredin, P.; Mortier, M.; Van Tendeloo, G.; Moshchalkov, V.V.
Title	Ultralow blocking temperature and breakdown of the giant spin model in Er³⁺-doped nanoparticles			Type	A1 Journal article
Year	2010	Publication	Physical review : B : condensed matter and materials physics	Abbreviated Journal	Phys Rev B
Volume	82	Issue	9	Pages	094421-094421,8
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	The magnetization of luminescent Er3+-doped PbF2 nanoparticles (formula Er0.3Pb0.7F2.3) has been studied. Despite the high concentration of the doping Er3+ ions and relatively large size (8 nm) of these nanoparticles we have found no deviation between field-cooled and zero-field-cooled magnetization curves down to T=0.35 K, which points out an ultralow blocking temperature for the reversal of magnetization. We also have found strongly deviating magnetization curves M(H/T) for different temperatures T. These results altogether show that the investigated nanoparticles are not superparamagnetic, but rather each Er3+ ion in these nanoparticles is found in a paramagnetic state down to very low temperatures, which implies the breakdown of the Néel-Brown giant spin model in the case of these nanoparticles. Calculations of magnetization within a paramagnetic model of noninteracting Er3+ ions completely support this conclusion. Due to the ultralow blocking temperature, these nanoparticles have a potential for magnetic field-induced nanoscale refrigeration with an option of their optical localization and temperature control.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000281773300005	Publication Date	2010-09-13
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	1098-0121;1550-235X;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.836	Times cited	11	Open Access
Notes	Fwo			Approved	Most recent IF: 3.836; 2010 IF: 3.774
Call Number	UA @ lucian @ c:irua:85423			Serial	3796
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Author	Gehrke, K.; Moshnyaga, V.; Samwer, K.; Lebedev, O.I.; Verbeeck, J.; Kirilenko, D.; Van Tendeloo, G.
Title	Interface controlled electronic variations in correlated heterostructures			Type	A1 Journal article
Year	2010	Publication	Physical review : B : condensed matter and materials physics	Abbreviated Journal	Phys Rev B
Volume	82	Issue	11	Pages	113101,1-113101,4
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	An interface modification of (LaCa)MnO3-BaTiO3 superlattices was found to massively influence magnetic and magnetotransport properties. Moreover it determines the crystal structure of the manganite layers, changing it from orthorhombic (Pnma) for the conventional superlattice (cSL), to rhombohedral (R3̅ c) for the modified one (mSL). While the cSL shows extremely nonlinear ac transport, the mSL is an electrically homogeneous material. The observations go beyond an oversimplified picture of dead interface layers and evidence the importance of electronic correlations at perovskite interfaces.
Address
Corporate Author				Thesis
Publisher		Place of Publication		Editor
Language		Wos	000281643200001	Publication Date	2010-09-07
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	1098-0121;1550-235X;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.836	Times cited	9	Open Access
Notes	This work was supported by DFG via SFB 602, TPA2.			Approved	Most recent IF: 3.836; 2010 IF: 3.774
Call Number	UA @ lucian @ c:irua:84249UA @ admin @ c:irua:84249			Serial	1691
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Author	Chen, L.; Kirilenko, D.; Stesmans, A.; Nguyen, X.S.; Binnemans, K.; Goderis, B.; Vanacken, J.; Lebedev, O.; Van Tendeloo, G.; Moshchalkov, V.V.
Title	Symmetry and electronic states of Mn²⁺ in ZnS nanowires with mixed hexagonal and cubic stacking			Type	A1 Journal article
Year	2010	Publication	Applied physics letters	Abbreviated Journal	Appl Phys Lett
Volume	97	Issue	4	Pages	041918,1-041918,3
Keywords	A1 Journal article; Electron microscopy for materials research (EMAT)
Abstract	Electron spin resonance and electronic spectroscopy techniques were used to study the symmetry and electronic structure of Mn2+ dopants in solvothermally synthesized ZnS nanowires. The average diameter of ∼ 5 nm leads to the observable quantum confinement effects in the photoluminescence excitation spectra. The results clearly demonstrate the three symmetry locations of Mn2+ incorporation. Together with the inferred Mn2+ center densities, these data indicate a much higher efficiency of Mn2+ substitution in the nanowire sample with about two times larger diameter.
Address
Corporate Author				Thesis
Publisher	American Institute of Physics	Place of Publication	New York, N.Y.	Editor
Language		Wos	000281059200038	Publication Date	2010-08-02
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0003-6951;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	3.411	Times cited	5	Open Access
Notes	Methusalem			Approved	Most recent IF: 3.411; 2010 IF: 3.841
Call Number	UA @ lucian @ c:irua:84869			Serial	3403
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Author	Razdobarin, A.G.; Mukhin, E.E.; Semenov, V.V.; Yu.Tolstyakov, S.; Kochergin, M.M.; Kurskiev, G.S.; Podushnikova, K.A.; Kirilenko, D.A.; Sitnikova, A.A.; Gorodetsky, А.Е.; Bukhovets, V.L.; Zalavutdinov, R.K.; Zakharov, А.P.; Arkhipov, I.I.; Voitsenya, V.S.; Bondarenko, V.N.; Konovalov, V.G.; Ryzhkov, I.V.;
Title	High reflective mirrors for in-vessel applications in ITER			Type	A1 Journal article
Year	2010	Publication	Nuclear instruments and methods in physics research : A: accelerators, spectrometers, detectors and associated equipment	Abbreviated Journal	Nucl Instrum Meth A
Volume	623	Issue	2	Pages	809-811
Keywords	A1 Journal article; Engineering sciences. Technology; Electron microscopy for materials research (EMAT)
Abstract	The structure and surface morphology of aluminum and silver mirrors covered with protective dielectric oxide layer were studied by means of TEM and SEM. The presence of needle-like pores throughout the thickness of the ZrO(2) film and bubble-like pores in Al(2)O(3) was observed. The test for resistivity to deuterium ion bombardment shows that the exposition to a fluence of similar to 2 x 10(20) ions/cm(2) with the ion energy of 40-50 eV results in appearance of blisters on the surface of mirrors covered wit h Al(2)O(3). For the mirrors protected with ZrO(2) no noticeable changes in surface morphology and reflectivity were found even after order of magnitude higher ion fluence. The effect of different porous structures on blistering phenomena is discussed. (C) 2010 Elsevier B.V. All rights reserved.
Address
Corporate Author				Thesis
Publisher	Elsevier Science	Place of Publication	Amsterdam	Editor
Language		Wos	000284343600041	Publication Date	2010-04-22
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0168-9002;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	1.362	Times cited	4	Open Access
Notes				Approved	Most recent IF: 1.362; 2010 IF: 1.142
Call Number	UA @ lucian @ c:irua:95545			Serial	1442
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Author	Afanasov, I.M.; Shornikova, O.N.; Kirilenko, D.A.; Vlasov, I.I.; Zhang, L.; Verbeeck, J.; Avdeev, V.V.; Van Tendeloo, G.
Title	Graphite structural transformations during intercalation by HNO₃ and exfoliation			Type	L1 Letter to the editor
Year	2010	Publication	Carbon	Abbreviated Journal	Carbon
Volume	48	Issue	6	Pages	1862-1865
Keywords	L1 Letter to the editor; Electron microscopy for materials research (EMAT)
Abstract	Expandable graphite of two types was synthesized by (1) hydrolysis of graphite nitrate of II stage and (2) anodic polarization of graphite in 60% HNO3. Exfoliated graphite samples were produced by thermal shock of expandable graphite samples in air at 900 °C. A comparative study of microstructural distinctions of both expandable and exfoliated graphite samples was carried out using X-ray diffraction, Raman spectroscopy, electron energy loss spectroscopy and high resolution transmission electron microscopy.
Address
Corporate Author				Thesis
Publisher		Place of Publication	Oxford	Editor
Language		Wos	000276132800021	Publication Date	2010-02-02
Series Editor		Series Title		Abbreviated Series Title
Series Volume		Series Issue		Edition
ISSN	0008-6223;	ISBN		Additional Links	UA library record; WoS full record; WoS citing articles
Impact Factor	6.337	Times cited	43	Open Access
Notes				Approved	Most recent IF: 6.337; 2010 IF: 4.896
Call Number	UA @ lucian @ c:irua:82315UA @ admin @ c:irua:82315			Serial	1379
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