Retrieval of B1 phase from high-pressure B2 phase for CdO nanoparticles by electronic excitations in Cd_xZn_1−xO composite thin films

• Arkaprava Das,
• Marcin Zając and
• Carla Bittencourt

Beilstein J. Nanotechnol. 2025, 16, 551–560, doi:10.3762/bjnano.16.43

• electrostatic repulsion among charged ions, which exceeds the chemical bond energy of the host lattice, ultimately leading to amorphization. The second model incorporates the concept of radial energy distribution to account for track formation. Within the framework of the inelastic thermal spike model, energy

• 120 MeV silver ion irradiation. The subsequent two coupled differential equations describe the energy distribution within the electronic and lattice subsystems, framed within cylindrical geometry, and represent the transient thermal process involved: Equation 2 corresponds to the energy transfer to

Investigation on drag reduction on rotating blade surfaces with microtextures

• Qinsong Zhu,
• Chen Zhang,
• Fuhang Yu and
• Yan Xu

Beilstein J. Nanotechnol. 2024, 15, 833–853, doi:10.3762/bjnano.15.70

• left corner of each panel. (a) Static pressure and (b) turbulent kinetic energy distribution of blade surfaces with different groove parameters. Influence of (a) height, (b) width, and (c) spacing of microtextures on drag reduction performance. The effect of microtexture on (a) turbulent kinetic energy

Electron-induced ligand loss from iron tetracarbonyl methyl acrylate

• Hlib Lyshchuk,
• Atul Chaudhary,
• Thomas F. M. Luxford,
• Miloš Ranković,
• Jaroslav Kočišek,
• Juraj Fedor,
• Lisa McElwee-White and
• Pamir Nag

Beilstein J. Nanotechnol. 2024, 15, 797–807, doi:10.3762/bjnano.15.66

• beam is produced from a directly heated yttrium-coated iridium cathode, and a trochoidal electron monochromator is used to narrow down the electron energy distribution and to produce a quasi-monochromatic electron beam. A gas-phase effusive beam was produced by introducing the liquid Fe(CO)4MA sample

Level set simulation of focused ion beam sputtering of a multilayer substrate

• Alexander V. Rumyantsev,
• Nikolai I. Borgardt,
• Roman L. Volkov and
• Yuri A. Chaplygin

Beilstein J. Nanotechnol. 2024, 15, 733–742, doi:10.3762/bjnano.15.61

• the sputtered atoms possess rather low energy with the peak value close to the surface binding energy [31], the sputtering of materials induced by these particles was assumed to be negligible. The energy distribution of sputtered atoms also was ignored in the description of their sticking to the

• functions where and are angular and energy distribution functions normalized to unity. Since backscattered ions have a sufficiently wide energy range, their impact on the sample surface causes additional sputtering of the target atoms. Similarly to [24], the function was applied for calculating the

• underestimation of the depths of the experimentally fabricated structures. The energy distribution functions for incident angles θ > 70° were found by SDTrimSP simulations by dividing the energy range of backscattered ions into intervals with a step of 3 keV and calculating the normalized number of particles

Investigating ripple pattern formation and damage profiles in Si and Ge induced by 100 keV Ar⁺ ion beam: a comparative study

• Indra Sulania,
• Harpreet Sondhi,
• Tanuj Kumar,
• Sunil Ojha,
• G R Umapathy,
• Ambuj Mishra,
• Ambuj Tripathi,
• Richa Krishna,
• Devesh Kumar Avasthi and
• Yogendra Kumar Mishra

Beilstein J. Nanotechnol. 2024, 15, 367–375, doi:10.3762/bjnano.15.33

• and energy of the incoming ion and on the mass of the target atom. It may be expressed as the spatial distribution of the energy transferred/deposited within the target [27][28]. Sometimes the energy distribution on the target atoms at the surface may be sufficient to overcome binding energies so as

• processes (i.e., thermal diffusion and ion-induced diffusion) [32]. This approach is based on the linear cascade model and Gaussian approximation of energy distribution as developed by Sigmund [26] to describe ion–atom collisions inside the target. Rutherford backscattering spectrometry (RBS) studies in the

A combined gas-phase dissociative ionization, dissociative electron attachment and deposition study on the potential FEBID precursor [Au(CH₃)₂Cl]₂

• Elif Bilgilisoy,
• Ali Kamali,
• Thomas Xaver Gentner,
• Gerd Ballmann,
• Sjoerd Harder,
• Hans-Peter Steinrück,
• Hubertus Marbach and
• Oddur Ingólfsson

Beilstein J. Nanotechnol. 2023, 14, 1178–1199, doi:10.3762/bjnano.14.98

• hydrochloric acid and/or chloromethane plays an important role in these fragmentation processes. In FEBID, the effective damage yield [28][49] for a specific precursor will be a convolution of the energy distribution of the electrons involved (i.e., of the primary, secondary, and inelastic scattered electrons

Plasmonic nanotechnology for photothermal applications – an evaluation

• A. R. Indhu,
• L. Keerthana and
• Gnanaprakash Dharmalingam

Beilstein J. Nanotechnol. 2023, 14, 380–419, doi:10.3762/bjnano.14.33

• ultimate conversion of electron scattering into heat. The energy distribution of hot carriers (which decides the relaxation times) depends on the electronic band structure [78], particle size, density of states, and the geometry of nanoparticles [79]. Figure 12 shows the vast differences in the population

High–low Kelvin probe force spectroscopy for measuring the interface state density

• Ryo Izumi,
• Masato Miyazaki,
• Yan Jun Li and
• Yasuhiro Sugawara

Beilstein J. Nanotechnol. 2023, 14, 175–189, doi:10.3762/bjnano.14.18

• by the CPD, is applied to the semiconductor sample. Therefore, the surface potential of the semiconductor is fixed at a certain energy, and only the surface state near the Fermi level of the surface is reflected in CPD measurements, making measurement of the energy distribution of the interface

• states within the bandgap difficult. Thus, a method for measuring the energy distribution of the interface states must be developed. Kelvin probe force spectroscopy (KPFS) or electrostatic force spectroscopy is a technique that enables energy spectroscopy of interface states in the semiconductor bandgap

• the localized energy levels of insulating layers on semiconductor surfaces has been reported to be feasible [22]. Therefore, we can expect that the KPFS method described above can be combined with high–low KPFM to measure the energy distribution of the interface states. In this study, we propose high

Impact of device design on the electronic and optoelectronic properties of integrated Ru-terpyridine complexes

• Max Mennicken,
• Sophia Katharina Peter,
• Corinna Kaulen,
• Ulrich Simon and
• Silvia Karthäuser

Beilstein J. Nanotechnol. 2022, 13, 219–229, doi:10.3762/bjnano.13.16

• -complex wire devices and decline with ascending voltage from EA = 75 meV at 0.1 V to 64 meV at 1 V (see also Supporting Information File 1, Figure S7). This small decline in EA can be attributed to the broadening of the electron energy distribution at the Fermi level, that is, the temperature-dependent

Low-energy electron interaction and focused electron beam-induced deposition of molybdenum hexacarbonyl (Mo(CO)₆)

• Po-Yuan Shih,
• Maicol Cipriani,
• Christian Felix Hermanns,
• Jens Oster,
• Klaus Edinger,
• Armin Gölzhäuser and
• Oddur Ingólfsson

Beilstein J. Nanotechnol. 2022, 13, 182–191, doi:10.3762/bjnano.13.13

• electrons (SEs) are produced [8][9]. Usually, the energy distribution of these SEs has a peak intensity well below 10 eV, with contributions close to 0 eV and falls rapidly off towards higher energies [9][10]. The secondary electrons are very reactive species, and in fact, the decomposition of the precursor

• -induced processes. The secondary electron energy distribution is not largely influenced by the primary electron energy [10]. However, in a W(CO)6 FEBID deposition at 5 keV, Mulders et al. [59] reported close to 37 atom % of W and C and about 27% O at room temperature. At about 150 °C, they reported about

Irradiation-driven molecular dynamics simulation of the FEBID process for Pt(PF₃)₄

• Alexey Prosvetov,
• Alexey V. Verkhovtsev,
• Gennady Sushko and
• Andrey V. Solov’yov

Beilstein J. Nanotechnol. 2021, 12, 1151–1172, doi:10.3762/bjnano.12.86

• evaluated by means of analytical models [41]. The obtained spatial and energetic distributions of PE, SE, and BSE are tabulated. The spatial distribution of electrons is defined on a cubic grid covering the whole simulation box; the grid consists of voxels with the size of 1 nm. The energy distribution of

Controlling the electronic and physical coupling on dielectric thin films

• Philipp Hurdax,
• Michael Hollerer,
• Larissa Egger,
• Georg Koller,
• Xiaosheng Yang,
• Anja Haags,
• Serguei Soubatch,
• Frank Stefan Tautz,
• Mathias Richter,
• Alexander Gottwald,
• Peter Puschnig,
• Martin Sterrer and
• Michael G. Ramsey

Beilstein J. Nanotechnol. 2020, 11, 1492–1503, doi:10.3762/bjnano.11.132

• function decrease and, therefore, the desorption of charged molecules happens already within the desorption regime of the neutral molecules. This might be explained by the spontaneous discharging as a result of the thermal energy distribution, enabling desorption as a neutral molecule. Conclusion While

Fabrication of Ag-modified hollow titania spheres via controlled silver diffusion in Ag–TiO₂ core–shell nanostructures

• Bartosz Bartosewicz,
• Malwina Liszewska,
• Bogusław Budner,
• Marta Michalska-Domańska,
• Krzysztof Kopczyński and
• Bartłomiej J. Jankiewicz

Beilstein J. Nanotechnol. 2020, 11, 141–146, doi:10.3762/bjnano.11.12

• hollow nanostructures show a broad and relatively strong absorption in the whole investigated spectral range, which corresponds to over 60% of the energy in the solar energy distribution [29]. The changes observed in the optical properties of the Ag-modified TiO2 HSs compared to Ag@TiO2 CSNs are related

Graphynes: an alternative lightweight solution for shock protection

• Kang Xia,
• Haifei Zhan,
• Aimin Ji,
• Jianli Shao,
• Yuantong Gu and
• Zhiyong Li

Beilstein J. Nanotechnol. 2019, 10, 1588–1595, doi:10.3762/bjnano.10.154

• panel), and the corresponding kinetic energy distribution pattern (right panel). The insert in the left panel shows the formation of initial cracks at the impact area; (b) stress distribution pattern right after perforation at 5.0 ps; and (c) the final atomic configuration at 6.4 ps. Impact deformation

• of different GYs under an impact velocity of 2 km/s. (a, b) Atomic configurations of β-GY: (a) von Mises atomic stress distribution pattern at a simulation time of 2.0 ps (left panel), and the corresponding kinetic energy distribution pattern (right panel); the insert in the left panel shows the

• formation of initial cracks at the impact area; and (b) final atomic configuration after 4.9 ps. (c, d) Atomic configurations of γ-GY: (c) von Mises atomic stress distribution pattern at a simulation time of 20 ps (left panel), and the corresponding kinetic energy distribution pattern (right panel); the

Energy distribution in an ensemble of nanoparticles and its consequences

• Dieter Vollath

Beilstein J. Nanotechnol. 2019, 10, 1452–1457, doi:10.3762/bjnano.10.143

• properties of such an “isothermal” ensemble can be predicted. The width of the energy distribution decreases with increasing particle size. This particle size dependence of the energy per particle controls phase fluctuations in the vicinity of the transformation temperature. Additionally, applying the

• quantity determining the width of the energy distribution is the heat capacity of the particles. For these calculations, bulk data for the heat capacity were successfully applied. This leads to the conclusion that the data for heat capacity of nanoparticles are very close to the bulk values. Keywords

• : energy distribution; isothermal ensemble; nanoparticle ensemble; normal distribution; particle size distribution; temperature distribution; Introduction General theoretical considerations about ensembles of nanoparticles assume that the ensemble is isothermal. To connect these theoretical considerations

Charged particle single nanometre manufacturing

• Philip D. Prewett,
• Cornelis W. Hagen,
• Claudia Lenk,
• Steve Lenk,
• Marcus Kaestner,
• Tzvetan Ivanov,
• Ahmad Ahmad,
• Ivo W. Rangelow,
• Xiaoqing Shi,
• Stuart A. Boden,
• Alex P. G. Robinson,
• Dongxu Yang,
• Sangeetha Hari,
• Marijke Scotuzzi and
• Ejaz Huq

Beilstein J. Nanotechnol. 2018, 9, 2855–2882, doi:10.3762/bjnano.9.266

• distribution, β being the standard deviation of the “backscattered” energy distribution and η being the ratio of forward scattered energy deposited to “backscattered” energy deposition in the resist. For values of R1 >> α, Equation 2 may be approximated to a linear relationship between ln Q and R12 (Equation 3

• being the exposure dose required to clear out the resist from the centre of the doughnut due to the proximity effect, Qp being the threshold dose required for full clearance of the resist, R1 being the inner radius of the doughnut, α being the standard deviation of the forward-scattered deposited energy

Effective sensor properties and sensitivity considerations of a dynamic co-resonantly coupled cantilever sensor

• Julia Körner

Beilstein J. Nanotechnol. 2018, 9, 2546–2560, doi:10.3762/bjnano.9.237

• . Furthermore, a slight asymmetry can be found in the curve which is due to the very different properties of the individual subsystems, and, consequently, leads to an asymmetric energy distribution in the coupled system which is reflected in the effective sensor properties. That is not only the case for the

Tunable fractional Fourier transform implementation of electronic wave functions in atomically thin materials

• Daniela Dragoman

Beilstein J. Nanotechnol. 2018, 9, 1828–1833, doi:10.3762/bjnano.9.174

• , i.e., if Ψ(x,y) = Ψ(x)exp(iκy), in the same potential energy distribution, such that the wave function is a solution of the equation where vF ≈ c/300 is the Fermi velocity. From Equation 6 it follows that, for slowly varying potential energy distributions, as assumed above, for which both components

• now unidentified, manifestation of the Berry phase in graphene [9][16]. Please note that for both, 2DEGs and graphene, Lα does not depend on the wave-vector component along the y direction, but only on the energy and the parameters of the potential energy distribution. This means that the wave

• simpler technological solution to achieve a parabolic potential energy distribution relies on segmented gate electrodes, composed of several metallic stripes with identical or different widths, as shown in Figure 2a and Figure 2b, respectively; the distance between electrodes, d, is assumed constant. In

Electron interactions with the heteronuclear carbonyl precursor H₂FeRu₃(CO)₁₃ and comparison with HFeCo₃(CO)₁₂: from fundamental gas phase and surface science studies to focused electron beam induced deposition

• Ragesh Kumar T P,
• Paul Weirich,
• Lukas Hrachowina,
• Marc Hanefeld,
• Ragnar Bjornsson,
• Helgi Rafn Hrodmarsson,
• Sven Barth,
• D. Howard Fairbrother,
• Michael Huth and
• Oddur Ingólfsson

Beilstein J. Nanotechnol. 2018, 9, 555–579, doi:10.3762/bjnano.9.53

• 0 eV (Figure 4a). At the PBE0/ma-def2-TZVP level of theory the threshold for this channel is found to be 1.2 eV, and we thus attribute this low intensity contribution to the high energy tail of the Maxwell–Boltzmann inner energy distribution at the current experimental conditions, T = 338 to 343 K

Electron interaction with copper(II) carboxylate compounds

• Michal Lacko,
• Peter Papp,
• Iwona B. Szymańska,
• Edward Szłyk and
• Štefan Matejčík

Beilstein J. Nanotechnol. 2018, 9, 384–398, doi:10.3762/bjnano.9.38

• electron ionization (EI), dissociative ionization (DI) [17][18][19] processes. Their kinetic energy is only a few eV, with energy distribution determined by the type of wafer and energy of primary beam [20][21]. Thorman et al. have compared gas phase and surface data on low energy electron interactions

Response under low-energy electron irradiation of a thin film of a potential copper precursor for focused electron beam induced deposition (FEBID)

• Leo Sala,
• Iwona B. Szymańska,
• Céline Dablemont,
• Anne Lafosse and
• Lionel Amiaud

Beilstein J. Nanotechnol. 2018, 9, 57–65, doi:10.3762/bjnano.9.8

• dependence on the energy is more structured in condensed phase, with three maxima at 3, 5 and 9 eV for the F− desorption from condensed C2F6. Here, the 1.5 eV peak dominates the ESD curves for both CF3 and CF3CF2 desorption in the low-energy range. Considering the energy distribution of the secondary

• importance under FEBID conditions, considering that the energy distribution for secondary electrons emitted in the direct vicinity of the irradiation spot strongly peaks in the range of 1–5 eV, and can take part in the whole dissociation process. The effective cross section for CF3 release from the complex

Interactions of low-energy electrons with the FEBID precursor chromium hexacarbonyl (Cr(CO)₆)

• Jusuf M. Khreis,
• João Ameixa,
• Filipe Ferreira da Silva and
• Stephan Denifl

Beilstein J. Nanotechnol. 2017, 8, 2583–2590, doi:10.3762/bjnano.8.258

• the desired metal, with the formation of non-defined deposits on the surface. When high-energy electrons interact with the surface, a cascade of low-energy electrons (LEE) and backscattered electrons are generated. Many chemical reactions can be triggered by those secondary electrons with an energy

• distribution characterised by a substantial fraction close to the ionization energy of FEBID precursors, peaking well below 10 eV and extending with appreciable intensities down to 0 eV [4]. The quality of the formed nanostructures is controlled and influenced by the interactions of the secondary and

Amplified cross-linking efficiency of self-assembled monolayers through targeted dissociative electron attachment for the production of carbon nanomembranes

• Sascha Koch,
• Christopher D. Kaiser,
• Paul Penner,
• Michael Barclay,
• Lena Frommeyer,
• Daniel Emmrich,
• Patrick Stohmann,
• Tarek Abu-Husein,
• Andreas Terfort,
• D. Howard Fairbrother,
• Oddur Ingólfsson and
• Armin Gölzhäuser

Beilstein J. Nanotechnol. 2017, 8, 2562–2571, doi:10.3762/bjnano.8.256

• ). The cross-linking may be induced directly by the primary electrons, where electron exposure is used in the cross-linking step. However, as mentioned above, backscattered and secondary electrons may also play a considerable role [18]. Typically, the energy distribution of such secondary electron peaks

• (Figure 1), however, can be traced back to the internal energy distribution in these molecules at the experimental temperature, that is, the formation of Cl− and Br− below their thermochemical threshold is attributed to the high energy tail of the respective Maxwell–Boltzmann distribution of internal

•  1, must thus be attributed to the high energy tail of the internal energy distribution of the respective biphenyls at the current experimental temperature. Comparing the relative electron dose dependence of the dehalogenation process in the SAMs (Figure 2) and the relative cross sections for this

Electron beam induced deposition of silacyclohexane and dichlorosilacyclohexane: the role of dissociative ionization and dissociative electron attachment in the deposition process

• Ragesh Kumar T P,
• Sangeetha Hari,
• Krishna K Damodaran,
• Oddur Ingólfsson and
• Cornelis W. Hagen

Beilstein J. Nanotechnol. 2017, 8, 2376–2388, doi:10.3762/bjnano.8.237

• , generating a flux of secondary electrons on the surface of objects with high aspect ratio as these are grown [8][9]. The energy distribution of the secondary electrons produced depends largely on the nature of the substrate [10][11], but also on the primary electron energy. However, it normally has similar

Comprehensive investigation of the electronic excitation of W(CO)₆ by photoabsorption and theoretical analysis in the energy region from 3.9 to 10.8 eV

• Mónica Mendes,
• Khrystyna Regeta,
• Filipe Ferreira da Silva,
• Nykola C. Jones,
• Søren Vrønning Hoffmann,
• Gustavo García,
• Chantal Daniel and
• Paulo Limão-Vieira

Beilstein J. Nanotechnol. 2017, 8, 2208–2218, doi:10.3762/bjnano.8.220

• statistical bond breaking, the former reminiscent of a repulsive dissociation character by the translational energy distribution of the first CO ligand, the latter correctly modelled by statistical product energy distributions [33]. High-resolution VUV photoabsorption spectrum of W(CO)6 in the photon energy