Nano Letters Journal Impact Factor & Information

Publisher: American Chemical Society, American Chemical Society

Journal description

A central forum for scientists involved in nanoscale research, among a wide range of disciplines that include physical and materials chemistry, biotechnology, and applied physics. Nano Letters reports on fundamental research in all branches of the theory and practice of nanoscience and nanotechnology. It will provide rapid disclosure of the key elements of a study, publishing preliminary, experimental, and theoretical results on the physical, chemical, and biological phenomena, processes and applications of structures within the nanoscale range. Areas of interest include: Synthesis and processing of organic, inorganic, and hybrid nanosized materials by physical, chemical, and biological methods; Modeling and simulation of synthetic, assembly, and interaction processes; Characterization of unique size properties; Realization and application of novel nanostructures and nanodevices. This is the second letters journal launched by ACS, following the 1999 release of Organic Letters, and charged with the same mission: To rapidly communicate preliminary significant research results.

Current impact factor: 13.59

Impact Factor Rankings

2015 Impact Factor Available summer 2016
2014 Impact Factor 13.592
2013 Impact Factor 12.94
2012 Impact Factor 13.025
2011 Impact Factor 13.198
2010 Impact Factor 12.186
2009 Impact Factor 9.991
2008 Impact Factor 10.371
2007 Impact Factor 9.627
2006 Impact Factor 9.96
2005 Impact Factor 9.847
2004 Impact Factor 8.449
2003 Impact Factor 6.144
2002 Impact Factor 5.033

Impact factor over time

Impact factor

Additional details

5-year impact 14.89
Cited half-life 4.90
Immediacy index 2.55
Eigenfactor 0.36
Article influence 4.89
Website Nano Letters website
Other titles Nano letters (Online), Nano letters
ISSN 1530-6992
OCLC 44445939
Material type Document, Periodical, Internet resource
Document type Internet Resource, Computer File, Journal / Magazine / Newspaper

Publisher details

American Chemical Society

  • Pre-print
    • Author cannot archive a pre-print version
  • Restrictions
    • Must obtain written permission from Editor
    • Must not violate ACS ethical Guidelines
  • Post-print
    • Author cannot archive a post-print version
  • Restrictions
    • If mandated by funding agency or employer/ institution
    • If mandated to deposit before 12 months, must obtain waiver from Institution/Funding agency or use AuthorChoice
    • 12 months embargo
  • Conditions
    • On author's personal website, pre-print servers, institutional website, institutional repositories or subject repositories
    • Non-Commercial
    • Must be accompanied by set statement (see policy)
    • Must link to publisher version
    • Publisher's version/PDF cannot be used
    • If mandated sooner than 12 months, must obtain waiver from Editors or use AuthorChoice
    • Reviewed on 07/08/2014
  • Classification
    ​ white

Publications in this journal

  • Shaked Rosenne · Eran Grinvald · Elijah Shirman · Lior Neeman · Sounak Dutta · Omri Bar-Elli · Regev Ben-Zvi · Eitan Oksenberg · Petr Milko · Vyacheslav Kalchenko · Haim Weissman · Dan Oron · Boris Rybtchinski
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    ABSTRACT: Facile molecular self-assembly affords a new family of organic nanocrystals that, counterintuitively, exhibit a significant nonlinear optical response (second harmonic generation, SHG) despite the relatively small molecular dipole moment of the constituent molecules. The nanocrystals are self-assembled in aqueous media from simple mono-substituted perylenediimide (PDI) molecular building blocks. Control over the crystal dimensions can be achieved via modification of the assembly conditions. The combination of a simple fabrication process with the ability to generate soluble SHG nanocrystals with tunable sizes may open new avenues in the area of organic SHG materials.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02010
  • Binh-Minh Nguyen · Brian S Swartzentruber · Yun Goo Ro · Shadi A Dayeh
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    ABSTRACT: Knowledge of nanoscale hetero-epitaxy is continually evolving as advances in material synthesis reveal new mechanisms that have not been theoretically predicted and are different than what is known about planar structures. In addition to a wide range of potential applications, core/shell nanowire structures offer a useful template to investigate hetero-epitaxy at the atomistic scale. We show that the growth of a Ge shell on a Si core can be tuned from the theoretically predicted island growth mode to a conformal, crystalline, and smooth shell by careful adjustment of growth parameters in a narrow growth window that has not been explored before. In the latter growth mode, Ge adatoms preferentially nucleate islands on the {113} facets of the Si core, which outgrow over the {220} facets. Islands on the low-energy {111} facets appear to have a nucleation delay compared to the {113} islands, however they eventually coalesce to form a crystalline conformal shell. Synthesis of epitaxial and conformal Si/Ge/Si core/multi-shell structures enables us to fabricate unique cylindrical ring nanowire field-effect transistors, which we demonstrate to have steeper on/off characteristics than conventional core/shell nanowire transistors.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02313
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    ABSTRACT: Identification of relevant reaction pathways in ever more complex composite materials and nanostructures poses a central challenge to computational materials discovery. Efficient global structure search, tailored to identify chemically-relevant intermediates, could provide the necessary first-principles atomistic insight to enable a rational process design. In this work we modify a common feature of global geometry optimization schemes by employing automatically-generated collective curvilinear coordinates. The similarity of these coordinates to molecular vibrations enhances the generation of chemically meaningful trial structures for covalently bound systems. In the application to hydrogenated Si clusters we concomitantly observe a significantly increased efficiency in identifying low-energy structures and exploit it for an extensive sampling of potential products of silicon-cluster soft landing on Si(001) surfaces.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b03388
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    ABSTRACT: The direct growth of III-V nanostructures on silicon has shown great promise in the integration of optoelectronics with silicon-based technologies. Our previous work showed that scaling up nanostructures to micro-size while maintaining high quality heterogeneous integration opens a pathway towards a complete photonic integrated circuit and high-efficiency cost-effective solar cells. In this paper, we present a thorough material study of novel metastable InP micropillars monolithically grown on silicon, focusing on two enabling aspects of this technology - the stress relaxation mechanism at the heterogeneous interface and the microstructure surface quality. Aberration-corrected transmission electron microscopy studies show that InP grows directly on silicon without any amorphous layer in between. A set of periodic dislocations is found at the hetero-interface, relaxing the 8% lattice mismatch between InP and Si. Single crystalline InP can therefore grow on top of the fully relaxed template, yielding high-quality micropillars with diameters expanding beyond 1µm. An interesting power-dependence trend of carrier recombination lifetimes was captured for these InP micropillars at room temperature, for the first time for micro/nano-structures. By simply combining internal quantum efficiency with carrier lifetime, we revealed the recombination dynamics of non-radiative and radiative portions separately. A very low surface recombination velocity of 1.1×10(3) cm/sec was obtained. In addition, we experimentally estimated the radiative recombination B coefficient of 2.0×10(-10) cm(3)/sec for pure wurtzite-phased InP. These values are comparable with those obtained from InP bulk. Exceeding the limits of conventional nanowires, our InP micropillars combine the strengths of both nanostructures and bulk materials, and will provide an avenue in heterogeneous integration of III-V semiconductor materials onto silicon platforms.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02869
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    ABSTRACT: The relationship between photostability and conformation of 2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylene vinylene (MEH-PPV) conjugated polymers was studied via excitation polarization modulation depth (M) measurements. Upon partial photobleaching, M distributions of collapsed, highly ordered MEH-PPV molecules shifted towards lower values. Conversely, M distributions of MEH-PPV molecules with random coil conformations moved towards higher values after partial photobleaching. Monte Carlo simulations of randomly distributed dipole moments along polymer chains subjected to partial photobleaching revealed that a statistical effect leads to an increase in peak M value. Decreases in M values seen experimentally in the population of MEH-PPV molecules with high M values, however, are due to conformation-dependent photostability within single MEH-PPV polymers. We show that while folded MEH-PPV molecules are relatively more photostable than extended MEH-PPV molecules in an ensemble, extended portions of particular molecules are more photostable than folded domains within single MEH-PPV molecules.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b03409
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    ABSTRACT: We demonstrate two-color nano-emitters that enable the selection of the dominant emitting wavelength by varying the polarization of excitation light. The nano-emitters were fabricated via surface plasmon-triggered two-photon polymerization. By using two polymerizable solutions with different quantum dots, emitters of different colors can be positioned selectively in different orientations in the close vicinity of the metal nanoparticles. The dominant emission wavelength of the metal/polymer anisotropic hybrid nano-emitter can thus be selected by altering the incident polarization.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02962
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    ABSTRACT: The development of synthetic nanomotors for technological applications in particular for life science and nanomedicine is a key focus of current basic research. However, it has been challenging to make active nanosystems based on biocompatible materials consuming nontoxic fuels for providing self-propulsion. Here, we fabricate self-propelled Janus nanomotors based on hollow mesoporous silica nanoparticles (HMSNPs), which are powered by biocatalytic reactions of three different enzymes: catalase, urease, and glucose oxidase (GOx). The active motion is characterized by a mean-square displacement (MSD) analysis of optical video recordings and confirmed by dynamic light scattering (DLS) measurements. We found that the apparent diffusion coefficient was enhanced by up to 83%. In addition, using optical tweezers, we directly measured a holding force of 64 ± 16 fN, which was necessary to counteract the effective self-propulsion force generated by a single nanomotor. The successful demonstration of biocompatible enzyme-powered active nanomotors using biologically benign fuels has a great potential for future biomedical applications.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b03100
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    ABSTRACT: An IR-driven photocatalytic water splitting system based on WO2-NaxWO3 (x > 0.25) hybrid conductor materials was established for the first time; this system can be directly applied in sea water. The WO2-NaxWO3 (x > 0.25) hybrid conductor material was readily prepared by a high-temperature reduction process of semiconductor NaxWO3 (x < 0.25) nanowire bundles. A novel ladder-type carrier transfer process is suggested for the established IR-driven photocatalytic water splitting system.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b01581
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    ABSTRACT: The development of advanced stimuli-responsive systems for medicine, catalysis or technology requires compartmentalized reaction spaces with triggered activity. Only very few stimuli-responsive systems preserve the compartment architecture, and none allows a triggered activity in situ. We present here a biomimetic strategy to molecular transmembrane transport by engineering synthetic membranes equipped with channel proteins so that they are stimuli-responsive. Nanoreactors with triggered activity were designed by simultaneously encapsulating an enzyme inside polymer compartments, and inserting protein “gates” in the membrane. The outer membrane protein F (OmpF) porin was chemically modified with a pH-responsive molecular cap to serve as “gate” producing pH-driven molecular flow through the membrane, and control the in situ enzymatic activity. This strategy provides complex reaction spaces necessary in “smart” medicine and for biomimetic engineering of artificial cells.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b03386
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    ABSTRACT: Recently, there has been much interest in the extraction of hot electrons generated from surface plasmon decay as this process can be used to achieve additional bandwidth for both photodetectors and photovoltaics. Hot electrons are typically injected into semiconductors over a Schottky barrier between the metal and semiconductor, enabling generation of photocurrent with below bandgap photon illumination. As a two-dimensional semiconductor single and few layer molybdenum disulfide (MoS2) has been demonstrated to exhibit internal photogain and therefore becomes an attractive hot electron acceptor. Here, we investigate hot electron-based photodetection in a device consisting of bilayer MoS2 integrated with a plasmonic antenna array. We demonstrate sub-bandgap photocurrent originating from the injection of hot electrons into MoS2 as well as photoamplification that yields a photogain of 10(5). The large photogain results in a photoresponsivity of 5.2 A/W, which is far above similar silicon-based hot electron photodetectors in which no photoamplification is present. This technique is expected to have potential use in future ultra-compact near-infrared photodetection and optical memory devices.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02866
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    ABSTRACT: Titanium dioxide (TiO2) has been extensively investigated as photoanode for water oxidation, as it is believed to be one of the most stable photoanode materials. Yet, we surprisingly found that TiO2 photoanodes (rutile nanowire, anatase nanotube and P25 nanoparticle film) suffered from substantial photocurrent decay in neutral (Na2SO4) as well as basic (KOH) electrolyte solution. Photoelectrochemical measurements togehter with electron microscopy studies performed on rutile TiO2 nanowire photoanode show that the photocurrent decay is due to photo-hole induced corrosion, which competes with water oxidation reaction. Further studies reveal that photocurrent decay profile in neutral and basic solutions are fundamentally different. Notably, the structural reconstruction of nanowire surface occurs simultaneously with the corrosion of TiO2 in KOH solution resulting in the formation of an amorphous layer of titanium hydroxide, which slows down the photocorrosion. Based on this discovery, we demonstrate that the photoelectrochemical stability of TiO2 photoanode can be significantly improved by intentionally coating an amorphous layer of titanium hydroxide on the nanowire surface. The pre-treated TiO2 photaonode exhibits an excellent photocurrent retention rate of 97% after testing in KOH solution for 72 hours, while in comparison the untreated sample lost 20% of photocurrent in 12 hours under the same measurement conditions. This work provides new insights in understanding of the photoelectrochemical stability of bare TiO2 photoanodes.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b03114
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    ABSTRACT: Intercalation of C60 molecules at the graphene-substrate interface by annealing leads to amorphous and crystalline intercalated structures. A comparison of topography and electronic structure with wrinkles and moiré patterns confirms intercalation. The intercalated molecules imprint a local strain/deformation on the graphene layer, whose magnitude is controlled by the intermolecular distance. The crystalline intercalated structure exhibits a superlattice peak in the local density of states. This work provides control of local strain in graphene.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02851
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    ABSTRACT: Electrostatically tunable negative differential resistance (NDR) is demonstrated in monolithic metal-semiconductor-metal (Al-Ge-Al) nanowire (NW) heterostructures integrated in back-gated field-effect transistors (FETs). Unambiguous signatures of NDR even at room temperature are attributed to intervalley electron transfer. At yet higher electric fields, impact ionization leads to an exponential increase of the current in the ⟨111⟩ oriented Ge NW segments. Modulation of the transfer rates, manifested as a large tunability of the peak-to-valley ratio (PVR) and the onset of impact ionization is achieved by the combined influences of electrostatic gating, geometric confinement, and heterojunction shape on hot electron transfer and by electron-electron scattering rates that can be altered by varying the charge carrier concentration in the NW FETs.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b03169
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    ABSTRACT: Carbon allotropes are subject of intense investigations for their superb structural, electronic, and chemical properties, but not for topological band properties because of the lack of strong spin-orbit coupling (SOC). Here, we show that conjugated p orbital interactions, common to most carbon allotropes, can in principle produce a new type of topological band structure, forming the so-called Weyl-like semimetal in the absence of SOC. Taking a structurally stable interpenetrated graphene network (IGN) as example, we show, by first-principles calculations and tight-binding modeling, that its Fermi surface is made of two symmetry-protected Weyl-like loops with linear dispersion along perpendicular directions. These loops are reduced to Weyl-like points upon breaking of the inversion symmetry. Because of the topological properties of these band-structure anomalies, remarkably, at a surface terminated by vacuum there emerges a flat band in the loops case and two Fermi arcs in the points case. These topological carbon materials may also find applications in the fields of catalysts.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02978
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    ABSTRACT: With increasing interest in GaN based devices, the control and evaluation of doping are becoming more and more important. We have studied the structural and electrical properties of a series of Si-doped GaN nanowires (NWs) grown by molecular beam epitaxy (MBE) with a typical dimension of 2-3 µm in length, and 20-200 nm in radius. In particular, high resolution energy dispersive X-ray spectroscopy (EDX) has illustrated a higher Si incorporation in NWs than that in two-dimensional (2D) layers and Si segregation at the edge of the NW with the highest doping. Moreover, direct transport measurements on single NWs have shown a controlled doping with resistivity from 102 to 10-3 Ω.cm, and a carrier concentration from 1017 to 1020 cm-3. Field effect transistor (FET) measurements combined with finite element simulation by NextNano3 software have put in evidence the high mobility of carriers in the non-intentionally doped (NID) NWs.
    Nano Letters 10/2015; DOI:10.1021/acs.nanolett.5b02634
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    ABSTRACT: Despite the utmost importance and decades of experimental studies on fatigue in metallic glasses (MGs), there has been so far little or no atomic-level understanding of the mechanisms involved. Here we perform molecular dynamics simulations of tension-compression fatigue in Cu50Zr50 MGs under strain-controlled cyclic loading. It is shown that the shear band (SB) initiation under cyclic loading is distinctly different from that under monotonic loading. Under cyclic loading, SB initiation takes place when aggregates of shear transformation zones (STZs) accumulating at the MG surface reach a critical size comparable to the SB width, and the accumulation of STZs follows a power law with rate depending on the applied strain. It is further shown that almost the entire fatigue life of nanoscale MGs under low cycle fatigue is spent in the SB-initiation stage, similar to that of crystalline materials. Furthermore, a qualitative investigation of the effect of cycling frequency on the fatigue behavior of MGs suggests that higher cycling frequency leads to more cycles to failure. The present study sheds light on the fundamental fatigue mechanisms of MGs that could be useful in developing strategies for their engineering applications.
    Nano Letters 09/2015; DOI:10.1021/acs.nanolett.5b03045
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    ABSTRACT: The Stochastic Variational Method (SVM) is used to show that the effective mass model correctly estimates the binding energies of excitons and trions, but fails to predict the experimental binding energy of the biexciton. Using high-accuracy variational calculations, it is demonstrated that the biexciton binding energy in transition metal dichalcogenides is smaller than the trion binding energy, contradicting experimental findings. It is also shown that the biexciton has bound excited states and the binding energy of the $L=0$ excited state is in very good agreement with experimental data. This excited state corresponds to an hole attached to a negative trion and may be a possible resolution of the discrepancy between theory and experiment.
    Nano Letters 09/2015; DOI:10.1021/acs.nanolett.5b03009
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    ABSTRACT: Two-dimensional (2D) molybdenum disulfide (MoS2) has attracted significant attention recently due to its direct bandgap semiconducting characteristics. Experimental studies on monolayer MoS2 show that S vacancy concentration varies greatly; while recent theoretical studies show that the formation energy of S vacancy is high and thus its concentration should be low. We perform density functional theory calculations to study the structures and energetics of vacancy and interstitial in both grain boundary (GB) and grain interior (GI) in monolayer MoS2 and uncover an anomalous formation pathway for dislocation-double S vacancy (V2S) complexes in MoS2. In this pathway, a (5|7) defect in an S-polar GB energetically favorably converts to a (4|6) defect, which possesses a duality: dislocation and double S vacancy. Its dislocation character allows it to glide into GI through thermal activation at high temperatures, bringing the double vacancy with it. Our findings here not only explain why VS is predominant in exfoliated 2D MoS2 and V2S is predominant in CVD-grown 2D MoS2, but also reproduce GB patterns in CVD-grown MoS2. The new pathway for sulfur vacancy formation revealed here provides important insights and guidelines for controlling the quality of monolayer MoS2.
    Nano Letters 09/2015; DOI:10.1021/acs.nanolett.5b02769
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    ABSTRACT: We report on the first demonstration of InAs1-xSbx nanowires grown by catalyst-free selective-area metal-organic chemical vapor deposition (SA-MOCVD). Antimony composition as high as 15% is achieved, with strong photoluminescence at all compositions. The quality of the material is assessed by comparing the photoluminescence (PL) peak full-width at half-max (FWHM) of the nanowires to that of epitaxially grown InAsSb thin films on InAs. We find that the FWHM of the nanowires is only a few meV broader than epitaxial films, and a similar trend of relatively constant FWHM for increasing antimony composition is observed. Furthermore, the PL peak energy shows a strong dependence on temperature, suggesting wave-vector conserving transitions are responsible for the observed PL in spite of lattice mismatched growth on InAs substrate. This study shows that high-quality InAsSb nanowires can be grown by SA-MOCVD on lattice mismatched substrate, resulting in material suitable for infrared detectors and high performance nanoelectronic devices.
    Nano Letters 09/2015; DOI:10.1021/acs.nanolett.5b02389
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    ABSTRACT: Atomic force microscopy (AFM)-based single-molecule force spectroscopy (SMFS) is widely used to mechanically measure the folding and unfolding of proteins. However, the temporal resolution of a standard commercial cantilever is 50-1,000 mus, masking rapid transitions and short-lived intermediates. Recently, SMFS with 0.7-mus temporal resolution was achieved using an ultrashort (L = 9 microm) cantilever on a custom-built, high-speed AFM. By micromachining such cantilevers with a focused ion beam, we optimized them for SMFS rather than tapping-mode imaging. To enhance usability and throughput, we detected the modified cantilevers on a commercial AFM retrofitted with a detection laser system featuring a 3-mum circular spot size. Moreover, individual cantilevers were reused over multiple days. The improved capabilities of the modified cantilevers for SMFS were showcased by unfolding a polyprotein, a popular biophysical assay. Specifically, these cantilevers maintained a 1-mus response time while eliminating cantilever ringing (Q 0.5). We therefore expect such cantilevers, along with the instrumentational improvements to detect them on a commercial AFM, to accelerate high-precision AFM-based SMFS studies.
    Nano Letters 09/2015; DOI:10.1021/acs.nanolett.5b03166