Ultrahigh Vacuum

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Mark C. Hersam - One of the best experts on this subject based on the ideXlab platform.

  • Ultrahigh Vacuum self assembly of rotationally commensurate c8 btbt mos2 graphene mixed dimensional heterostructures
    Chemistry of Materials, 2019
    Co-Authors: Xiaolong Liu, Itamar Balla, Vinod K Sangwan, Hakan Usta, Antonio Facchetti, Tobin J Marks, Mark C. Hersam
    Abstract:

    Mixed-dimensional van der Waals heterostructures combine the advantages of nanomaterials with qualitatively distinct properties such as the extended bandstructures and high charge carrier mobilities of inorganic two-dimensional materials and the discrete orbital energy levels and strong optical absorption of zero-dimensional organic molecules. The synergistic interplay between nanomaterials of distinct dimensionality has enabled a variety of unique applications such as antiambipolar transistors, sensitized photodetectors, and gate-tunable photovoltaics. Because the performance of mixed-dimensional heterostructure devices depends sensitively on the buried interfacial structure, it is of great interest to identify materials and chemistries that naturally form highly ordered heterointerfaces. Toward this end, here we demonstrate Ultrahigh Vacuum self-assembly of 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT) monolayers onto epitaxial MoS2/graphene heterostructures. With molecular-resolution scan...

  • Ultrahigh Vacuum Self-Assembly of Rotationally Commensurate C8-BTBT/MoS2/Graphene Mixed-Dimensional Heterostructures
    2019
    Co-Authors: Xiaolong Liu, Itamar Balla, Vinod K Sangwan, Hakan Usta, Antonio Facchetti, Tobin J Marks, Mark C. Hersam
    Abstract:

    Mixed-dimensional van der Waals heterostructures combine the advantages of nanomaterials with qualitatively distinct properties such as the extended bandstructures and high charge carrier mobilities of inorganic two-dimensional materials and the discrete orbital energy levels and strong optical absorption of zero-dimensional organic molecules. The synergistic interplay between nanomaterials of distinct dimensionality has enabled a variety of unique applications such as antiambipolar transistors, sensitized photodetectors, and gate-tunable photovoltaics. Because the performance of mixed-dimensional heterostructure devices depends sensitively on the buried interfacial structure, it is of great interest to identify materials and chemistries that naturally form highly ordered heterointerfaces. Toward this end, here we demonstrate Ultrahigh Vacuum self-assembly of 2,7-dioctyl[1]­benzothieno­[3,2-b]­[1]­benzothiophene (C8-BTBT) monolayers onto epitaxial MoS2/graphene heterostructures. With molecular-resolution scanning tunneling microscopy and spectroscopy, the resulting C8-BTBT/MoS2/graphene mixed-dimensional heterostructures are found to be rotationally commensurate with well-defined physical and electronic structures. It is further shown that the self-assembled C8-BTBT monolayers are insensitive to the structural defects and electronic perturbations of the underlying MoS2 substrate, which provides significant processing latitude. For these reasons, this work will facilitate ongoing efforts to utilize organic/MoS2/graphene mixed-dimensional heterostructures for electronic, optoelectronic, and photovoltaic applications

  • probing intermolecular vibrational symmetry breaking in self assembled monolayers with Ultrahigh Vacuum tip enhanced raman spectroscopy
    Journal of the American Chemical Society, 2017
    Co-Authors: Naihao Chiang, Eric A. Pozzi, Nan Jiang, Mark C. Hersam, Tamar Seideman, George C. Schatz, Lindsey R Madison, Michael R Wasielewski, Mark A Ratner, Richard P Van Duyne
    Abstract:

    Ultrahigh Vacuum tip-enhanced Raman spectroscopy (UHV-TERS) combines the atomic-scale imaging capability of scanning probe microscopy with the single-molecule chemical sensitivity and structural specificity of surface-enhanced Raman spectroscopy. Here, we use these techniques in combination with theory to reveal insights into the influence of intermolecular interactions on the vibrational spectra of a N-N′-bis(2,6-diisopropylphenyl)-perylene-3,4:9,10-bis(dicarboximide) (PDI) self-assembled monolayer adsorbed on single-crystal Ag substrates at room temperature. In particular, we have revealed the lifting of a vibrational degeneracy of a mode of PDI on Ag(111) and Ag(100) surfaces, with the most strongly perturbed mode being that associated with the largest vibrational amplitude on the periphery of the molecule. This work demonstrates that UHV-TERS enables direct measurement of molecule–molecule interaction at nanoscale. We anticipate that this information will advance the fundamental understanding of the m...

  • Probing Intermolecular Vibrational Symmetry Breaking in Self-Assembled Monolayers with Ultrahigh Vacuum Tip-Enhanced Raman Spectroscopy
    2017
    Co-Authors: Naihao Chiang, Eric A. Pozzi, Nan Jiang, Mark C. Hersam, Tamar Seideman, George C. Schatz, Lindsey R Madison, Michael R Wasielewski, Mark A Ratner, Richard P Van Duyne
    Abstract:

    Ultrahigh Vacuum tip-enhanced Raman spectroscopy (UHV-TERS) combines the atomic-scale imaging capability of scanning probe microscopy with the single-molecule chemical sensitivity and structural specificity of surface-enhanced Raman spectroscopy. Here, we use these techniques in combination with theory to reveal insights into the influence of intermolecular interactions on the vibrational spectra of a N-N′-bis­(2,6-diisopropylphenyl)-perylene-3,4:9,10-bis­(dicarboximide) (PDI) self-assembled monolayer adsorbed on single-crystal Ag substrates at room temperature. In particular, we have revealed the lifting of a vibrational degeneracy of a mode of PDI on Ag(111) and Ag(100) surfaces, with the most strongly perturbed mode being that associated with the largest vibrational amplitude on the periphery of the molecule. This work demonstrates that UHV-TERS enables direct measurement of molecule–molecule interaction at nanoscale. We anticipate that this information will advance the fundamental understanding of the most important effect of intermolecular interactions on the vibrational modes of surface-bound molecules

  • Ultrahigh-Vacuum Tip-Enhanced Raman Spectroscopy
    Chemical reviews, 2016
    Co-Authors: Eric A. Pozzi, Nan Jiang, Tamar Seideman, Guillaume Goubert, Naihao Chiang, Craig T. Chapman, Michael O. Mcanally, Anne Isabelle Henry, George C. Schatz, Mark C. Hersam
    Abstract:

    Molecule–surface interactions and processes are at the heart of many technologies, including heterogeneous catalysis, organic photovoltaics, and nanoelectronics, yet they are rarely well understood at the molecular level. Given the inhomogeneous nature of surfaces, molecular properties often vary among individual surface sites, information that is lost in ensemble-averaged techniques. In order to access such site-resolved behavior, a technique must possess lateral resolution comparable to the size of surface sites under study, analytical power capable of examining chemical properties, and single-molecule sensitivity. Tip-enhanced Raman spectroscopy (TERS), wherein light is confined and amplified at the apex of a nanoscale plasmonic probe, meets these criteria. In Ultrahigh Vacuum (UHV), TERS can be performed in pristine environments, allowing for molecular-resolution imaging, low-temperature operation, minimized tip and molecular degradation, and improved stability in the presence of ultrafast irradiation...

Kentaro Kyuno - One of the best experts on this subject based on the ideXlab platform.

Masashi Iwatsuki - One of the best experts on this subject based on the ideXlab platform.

Seongju Park - One of the best experts on this subject based on the ideXlab platform.

  • effects of step graded alxga1 xn interlayer on properties of gan grown on si 111 using Ultrahigh Vacuum chemical vapor deposition
    Applied Physics Letters, 2001
    Co-Authors: Minho Kim, Hyon Chol Kang, Do Young Noh, Seongju Park
    Abstract:

    We report the growth of high-quality GaN on a Si(111) substrate using a five step-graded AlxGa1−xN (x=0.87–0.07) interlayer between GaN epilayer and AlN buffer layer by Ultrahigh Vacuum chemical vapor deposition. The crack density and the surface roughness of the GaN layer grown on the graded AlxGa1−xN interlayer were substantially reduced, compared to those of GaN grown on an AlN buffer layer. Significant improvement in the structural and optical properties of the GaN layer was also achieved by the use of a graded interlayer. These results are attributed to the decrease of the lattice mismatch between GaN and AlN layer, and the reduction of the thermal stress by the graded interlayer.

  • growth of high quality gan on si 111 substrate by Ultrahigh Vacuum chemical vapor deposition
    Applied Physics Letters, 2001
    Co-Authors: Minho Kim, Young Churl Bang, Naeman Park, Cheljong Choi, Tae Yeon Seong, Seongju Park
    Abstract:

    An Ultrahigh Vacuum chemical vapor deposition (UHVCVD) system was employed to grow high-quality GaN on a Si (111) substrate using a thin AlN buffer layer. X-ray diffraction, high-resolution electron microscopy (HREM), and photoluminescence (PL) data indicate that a single crystalline GaN layer with a wurtzite structure was epitaxially grown on a silicon substrate. The full width at half maximum (FWHM) of the x-ray rocking curve for the GaN (0002) diffraction was 16.7 arc min. A cross-sectional HREM image showed an amorphous SiNx layer at the Si/AlN interface, as well as stacking faults and inversion domain boundaries in the GaN epilayer. An intense PL emission line, which is associated with the recombination of the donor bound exciton, was observed at 10 K PL spectra (FWHM=6.8 meV) and a strong band edge emission was obtained (FWHM=33 meV) as well, even at room temperature. These results indicate that high-quality GaN can be grown on Si (111) substrates using a UHVCVD growth method.

Nan Jiang - One of the best experts on this subject based on the ideXlab platform.

  • angstrom scale chemical analysis of metal supported trans and cis regioisomers by Ultrahigh Vacuum tip enhanced raman mapping
    Nano Letters, 2019
    Co-Authors: Sayantan Mahapatra, Yingying Ning, Jeremy F Schultz, Junlong Zhang, Nan Jiang
    Abstract:

    Real space chemical analysis of two structurally very similar components, that is, regioisomers lies at the heart of heterogeneous catalysis reactions, modern-age electronic devices, and various other surface related problems in surface science and nanotechnology. One of the big challenges in surface chemistry is to identify different surface adsorbed molecules and analyze their chemical properties individually. Herein, we report a topological and chemical analysis of two regioisomers, trans- and cis-tetrakispentafluorophenylporphodilactone (trans- and cis-H2F20TPPDL) molecules by high-resolution scanning tunneling microscopy, and Ultrahigh Vacuum tip-enhanced Raman spectroscopy (UHV-TERS). Both isomeric structures are investigated individually on Ag(100) at liquid nitrogen temperature. Following that, we have successfully distinguished these two regioisomeric molecules simultaneously through TERS with an angstrom scale (8 A) spatial resolution. Also, the two-component organic heterojunction has been char...

  • probing intermolecular vibrational symmetry breaking in self assembled monolayers with Ultrahigh Vacuum tip enhanced raman spectroscopy
    Journal of the American Chemical Society, 2017
    Co-Authors: Naihao Chiang, Eric A. Pozzi, Nan Jiang, Mark C. Hersam, Tamar Seideman, George C. Schatz, Lindsey R Madison, Michael R Wasielewski, Mark A Ratner, Richard P Van Duyne
    Abstract:

    Ultrahigh Vacuum tip-enhanced Raman spectroscopy (UHV-TERS) combines the atomic-scale imaging capability of scanning probe microscopy with the single-molecule chemical sensitivity and structural specificity of surface-enhanced Raman spectroscopy. Here, we use these techniques in combination with theory to reveal insights into the influence of intermolecular interactions on the vibrational spectra of a N-N′-bis(2,6-diisopropylphenyl)-perylene-3,4:9,10-bis(dicarboximide) (PDI) self-assembled monolayer adsorbed on single-crystal Ag substrates at room temperature. In particular, we have revealed the lifting of a vibrational degeneracy of a mode of PDI on Ag(111) and Ag(100) surfaces, with the most strongly perturbed mode being that associated with the largest vibrational amplitude on the periphery of the molecule. This work demonstrates that UHV-TERS enables direct measurement of molecule–molecule interaction at nanoscale. We anticipate that this information will advance the fundamental understanding of the m...

  • Probing Intermolecular Vibrational Symmetry Breaking in Self-Assembled Monolayers with Ultrahigh Vacuum Tip-Enhanced Raman Spectroscopy
    2017
    Co-Authors: Naihao Chiang, Eric A. Pozzi, Nan Jiang, Mark C. Hersam, Tamar Seideman, George C. Schatz, Lindsey R Madison, Michael R Wasielewski, Mark A Ratner, Richard P Van Duyne
    Abstract:

    Ultrahigh Vacuum tip-enhanced Raman spectroscopy (UHV-TERS) combines the atomic-scale imaging capability of scanning probe microscopy with the single-molecule chemical sensitivity and structural specificity of surface-enhanced Raman spectroscopy. Here, we use these techniques in combination with theory to reveal insights into the influence of intermolecular interactions on the vibrational spectra of a N-N′-bis­(2,6-diisopropylphenyl)-perylene-3,4:9,10-bis­(dicarboximide) (PDI) self-assembled monolayer adsorbed on single-crystal Ag substrates at room temperature. In particular, we have revealed the lifting of a vibrational degeneracy of a mode of PDI on Ag(111) and Ag(100) surfaces, with the most strongly perturbed mode being that associated with the largest vibrational amplitude on the periphery of the molecule. This work demonstrates that UHV-TERS enables direct measurement of molecule–molecule interaction at nanoscale. We anticipate that this information will advance the fundamental understanding of the most important effect of intermolecular interactions on the vibrational modes of surface-bound molecules

  • Ultrahigh-Vacuum Tip-Enhanced Raman Spectroscopy
    Chemical reviews, 2016
    Co-Authors: Eric A. Pozzi, Nan Jiang, Tamar Seideman, Guillaume Goubert, Naihao Chiang, Craig T. Chapman, Michael O. Mcanally, Anne Isabelle Henry, George C. Schatz, Mark C. Hersam
    Abstract:

    Molecule–surface interactions and processes are at the heart of many technologies, including heterogeneous catalysis, organic photovoltaics, and nanoelectronics, yet they are rarely well understood at the molecular level. Given the inhomogeneous nature of surfaces, molecular properties often vary among individual surface sites, information that is lost in ensemble-averaged techniques. In order to access such site-resolved behavior, a technique must possess lateral resolution comparable to the size of surface sites under study, analytical power capable of examining chemical properties, and single-molecule sensitivity. Tip-enhanced Raman spectroscopy (TERS), wherein light is confined and amplified at the apex of a nanoscale plasmonic probe, meets these criteria. In Ultrahigh Vacuum (UHV), TERS can be performed in pristine environments, allowing for molecular-resolution imaging, low-temperature operation, minimized tip and molecular degradation, and improved stability in the presence of ultrafast irradiation...

  • conformational contrast of surface mediated molecular switches yields angstrom scale spatial resolution in Ultrahigh Vacuum tip enhanced raman spectroscopy
    Nano Letters, 2016
    Co-Authors: Naihao Chiang, Eric A. Pozzi, Nan Jiang, Mark C. Hersam, Tamar Seideman, Guillaume Goubert, Dhabih V Chulhai, Xing Chen, Xu Chen, Lasse Jensen
    Abstract:

    Tip-enhanced Raman spectroscopy (TERS) combines the ability of scanning probe microscopy (SPM) to resolve atomic-scale surface features with the single-molecule chemical sensitivity of surface-enhanced Raman spectroscopy (SERS). Here, we report additional insights into the nature of the conformational dynamics of a free-base porphyrin at room temperature adsorbed on a metal surface. We have interrogated the conformational switch between two metastable surface-mediated isomers of meso-tetrakis(3,5-ditertiarybutylphenyl)-porphyrin (H2TBPP) on a Cu(111) surface. At room temperature, the barrier between the porphyrin ring buckled up/down conformations of the H2TBPP-Cu(111) system is easily overcome, and a 2.6 A lateral resolution by simultaneous TERS and STM analysis is achieved under Ultrahigh Vacuum (UHV) conditions. This work demonstrates the first UHV-TERS on Cu(111) and shows TERS can unambiguously distinguish the conformational differences between neighboring molecules with Angstrom-scale spatial resolu...