Log in

Relevant bibliographies by topics / Platinum (111) / Journal articles

Journal articles on the topic 'Platinum (111)'

To see the other types of publications on this topic, follow the link: Platinum (111).

Author: Grafiati

Published: 11 March 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Platinum (111).'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Fecher, G. H., J. Bansmann, Ch Grünewald, A. Oelsner, Ch Ostertag, and G. Schönhense. "Oxidation of rubidium at platinum (111)." Surface Science 307-309 (April 1994): 70–75. http://dx.doi.org/10.1016/0039-6028(94)90372-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Kern, Klaus, Rudolf David, Robert L. Palmer, George Comsa, and Talat S. Rahman. "Surface phonon dispersion of platinum (111)." Physical Review B 33, no. 6 (March 15, 1986): 4334–37. http://dx.doi.org/10.1103/physrevb.33.4334.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Maurice, Vincent, and Christian Minot. "Theoretical investigation of the mechanisms for olefinic hydrogenation on platinum(110) and platinum(111) surfaces." Journal of Physical Chemistry 94, no. 23 (November 1990): 8579–88. http://dx.doi.org/10.1021/j100386a018.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Jo, Sam K., and John M. White. "Correlation of photoelectron yields and photodissociation rates of chloromethane on platinum(111) and carbon-covered platinum(111)." Journal of Physical Chemistry 94, no. 17 (August 1990): 6852–54. http://dx.doi.org/10.1021/j100380a057.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Komine, Nobuyuki, Tomoko Ishiwata, Jun-ya Kasahara, Erino Matsumoto, Masafumi Hirano, and Sanshiro Komiya. "Synthesis and organic group transfer of organodiplatinum complex with a 1,2-bis(diphenylphosphino)ethane ligand." Canadian Journal of Chemistry 87, no. 1 (January 1, 2009): 176–82. http://dx.doi.org/10.1139/v08-111.

Full text

Abstract:

A series of homometallic alkyl- and phenyldinuclear complexes containing one platinum–platinum bond, (dppe)RPt–Pt(η5-Cp)(CO) (R = Me, Et, CH2CMe3, Ph), have been prepared by oxidative addition of the Pt–C bond of PtR(η5-Cp) to Pt(styrene)(dppe), and were characterized by spectroscopic methods and (or) X-ray structure analysis. The geometry at Pt with a dppe ligand is square planar, and the carbonyl and Cp ligand of the Pt(η5-Cp)(CO) moiety lie orthogonal to the coordination plane of former platinum. Competitive organic group transfer reactions along the Pt–Pt bond in these complexes took place to give PtR(η5-Cp)(CO) and PtR(η1-Cp)(dppe) on thermolysis. Alkyl or aryl transfer from Pt with a dppe ligand were enhanced by addition of olefin, whereas treatment with CO and tertiary phosphine ligands causes Cp transfer from Pt(η5-Cp)(CO).Key words: organoplatinum–platinum complex, organic group transfer.

APA, Harvard, Vancouver, ISO, and other styles

6

Garbe, J., and J. Kirschner. "Spin-dependent photoemission intensities from platinum (111)." Physical Review B 39, no. 14 (May 15, 1989): 9859–64. http://dx.doi.org/10.1103/physrevb.39.9859.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Jiang, L. Q., and Bruce E. Koel. "Hydrocarbon trapping and condensation on platinum (111)." Journal of Physical Chemistry 96, no. 22 (October 1992): 8694–97. http://dx.doi.org/10.1021/j100201a008.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Diebold, Ulrike, Lanping Zhang, John F. Anderson, and Pawel Mrozek. "Surface segregation of silicon in platinum(111)." Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films 14, no. 3 (May 1996): 1679–83. http://dx.doi.org/10.1116/1.580318.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Tachibana, Takeshi, Yoshihiro Yokota, Koichi Miyata, Takashi Onishi, Koji Kobashi, Masayoshi Tarutani, Yoshizo Takai, Ryuichi Shimizu, and Yoshihiro Shintani. "Diamond films heteroepitaxially grown on platinum (111)." Physical Review B 56, no. 24 (December 15, 1997): 15967–81. http://dx.doi.org/10.1103/physrevb.56.15967.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Tachibana, Takeshi, Yoshihiro Yokota, Koichi Miyata, Koji Kobashi, and Yoshihiro Shintani. "Heteroepitaxial diamond growth process on platinum (111)." Diamond and Related Materials 6, no. 2-4 (March 1997): 266–71. http://dx.doi.org/10.1016/s0925-9635(96)00733-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Arulmozhi, Nakkiran, Thomas J. P. Hersbach, and Marc T. M. Koper. "Nanoscale morphological evolution of monocrystalline Pt surfaces during cathodic corrosion." Proceedings of the National Academy of Sciences 117, no. 51 (December 7, 2020): 32267–77. http://dx.doi.org/10.1073/pnas.2017086117.

Full text

Abstract:

This paper studies the cathodic corrosion of a spherical single crystal of platinum in an aqueous alkaline electrolyte, to map out the detailed facet dependence of the corrosion structures forming during this still largely unexplored electrochemical phenomenon. We find that anisotropic corrosion of the platinum electrode takes place in different stages. Initially, corrosion etch pits are formed, which reflect the local symmetry of the surface: square pits on (100) facets, triangular pits on (111) facets, and rectangular pits on (110) facets. We hypothesize that these etch pits are formed through a ternary metal hydride corrosion intermediate. In contrast to anodic corrosion, the (111) facet corrodes the fastest, and the (110) facet corrodes the slowest. For cathodic corrosion on the (100) facet and on higher-index surfaces close to the (100) plane, the etch pit destabilizes in a second growth stage, by etching faster in the (111) direction, leading to arms in the etch pit, yielding a concave octagon-shaped pit. In a third growth stage, these arms develop side arms, leading to a structure that strongly resembles a self-similar diffusion-limited growth pattern, with strongly preferred growth directions.

APA, Harvard, Vancouver, ISO, and other styles

12

Wieghold, Sarah, Lea Nienhaus, Armin Siebel, Maximilian Krause, Patricia Wand, Martin Gruebele, Ueli Heiz, and Friedrich Esch. "Au(111)-supported Platinum Nanoparticles: Ripening and Activity." MRS Advances 2, no. 8 (2017): 439–44. http://dx.doi.org/10.1557/adv.2017.75.

Full text

Abstract:

ABSTRACTThe recent spotlight on supported nanoparticles (NPs) has attracted attention in the field of catalysis and fuel cell technology. Supported NPs can be used as model catalysts to gain a fundamental understanding of the catalytic properties at the interface. Here, especially the wet-chemical preparation of platinum NPs in alkaline ethylene glycol is a powerful approach to synthesize stable particles with a narrow size distribution in the nanometer regime. We combine high resolution imaging by scanning tunneling microscopy with electrochemical characterization by cyclic voltammetry to gain insights into the underlying degradation mechanism of supported platinum NPs, paving the way toward a rational design of supported catalysts with controlled activity and stability.

APA, Harvard, Vancouver, ISO, and other styles

13

yokota, Y., and H. Hashimoto. "Formation process of silicide at Pt-Si (111) interface." Proceedings, annual meeting, Electron Microscopy Society of America 46 (1988): 484–85. http://dx.doi.org/10.1017/s0424820100104480.

Full text

Abstract:

The initial stage of the reaction process forming the platinum silicide at Pt/Si (111) interfaces have been investigated by a high resolution electron microscope in both “flat-on” [1] and “cross-sectional” mode.First, platinum of 11 nm thickness was deposited on a Si (111) wafer. For observing the specimen in “flat-on” mode, the top surface and edge of the specimen were covered by paraffin and etched chemically using CP-4 reagent from backside. The specimen for observing in “cross-sectional” mode was prepared as follows. The Si wafer was cut into slips of 3mm width. After stacking 4 to 6 slips together with epoxy resin, the stacks were sliced to a thickness of 0.3-0.4mm by a diamond saw. The slices were mechanically polished to a thickness lower than 0.05mm and then thinned by Ar ion beam.The formation process of platinum silicide (PtSi) was observed in a cross-sectional specimen.

APA, Harvard, Vancouver, ISO, and other styles

14

Janssens, T. V. W., and F. Zaera. "Chemistry of Ethylidene Moieties on Platinum Surfaces: 1,1-Diiodoethane on Pt(111)." Journal of Physical Chemistry 100, no. 33 (January 1996): 14118–29. http://dx.doi.org/10.1021/jp960910w.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Pašti, Igor A., Nemanja M. Gavrilov, and Slavko V. Mentus. "Hydrogen Adsorption on Palladium and Platinum Overlayers: DFT Study." Advances in Physical Chemistry 2011 (July 10, 2011): 1–8. http://dx.doi.org/10.1155/2011/305634.

Full text

Abstract:

Hydrogen adsorption on twenty different palladium and platinum overlayer surfaces with (111) crystallographic orientation was studied by means of periodic DFT calculations on the GGA-PBE level. Palladium and platinum overlayers here denote either the Pd and Pt mono- and bilayers deposited over (111) crystallographic plane of Pd, Pt, Cu, and Au monocrystals or the (111) crystallographic plane of Pd and Pt monocrystals with inserted one-atom-thick surface underlayer of Pd, Pt, Cu, and Au. The attention was focused on the bond lengths, hydrogen adsorption energetics, mobility of adsorbed hydrogen, and surface reactivity toward hydrogen electrode reactions. Both the ligand and strain effects were considered, found to lead to a significant modification of the electronic structure of Pd and Pt overlayers, described through the position of the d-band center, and tuning of the hydrogen adsorption energy in the range that covers approximately 120 kJmol−1. Mobility of hydrogen adsorbed on studied overlayers was found to be determined by hydrogen-metal binding energy. Obtained results regarding Pd layers on Pt(111) and Au(111) surfaces, in conjunction with some of the recent experimental data, were used to explain its electrocatalytic activity towards hydrogen evolution reaction.

APA, Harvard, Vancouver, ISO, and other styles

16

Arend, Rebecca Christian, Bradley J. Monk, Thomas J. Herzog, Jonathan A. Ledermann, Kathleen N. Moore, Angeles Alvarez Secord, Ronnie Shapira-Frommer, et al. "Clinical trial in progress: Pivotal study of VB-111 combined with paclitaxel versus paclitaxel for treatment of platinum-resistant ovarian cancer (OVAL, VB-111-701/GOG-3018)." Journal of Clinical Oncology 39, no. 15_suppl (May 20, 2021): TPS5599. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.tps5599.

Full text

Abstract:

TPS5599 Background: Ofranergene obadenovec (VB-111) is a targeted anti-cancer gene therapy with a dual mechanism of action that includes a broad antiangiogenic effect and induction of a tumor directed immune response. A phase II trial in patients with platinum resistant ovarian cancer showed that VB-111 in combination with weekly paclitaxel was well tolerated and associated with a CA-125 Objective Response Rate (ORR) of 58% with a trend for improved survival. The favorable outcomes were associated with induction of an immunotherapeutic effect of tumor infiltration with CD-8 T cells. Based on these observations, a phase III study was initiated in collaboration with the GOG Foundation, Inc. Methods: Study NCT03398655 is an international, randomized, double-blind, placebo-controlled, phase III study. Eligible patients have recurrent platinum-resistant epithelial ovarian cancer with measurable disease (RECIST 1.1), and may have been previously treated with up to 5 prior lines of therapy. Patient are randomized 1:1 to receive VB-111 (1x1013 VPs) with weekly paclitaxel (80mg/m2), or weekly paclitaxel with placebo. Randomization is stratified by number of prior treatment lines, prior antiangiogenic therapy and platinum refractory disease status. The efficacy endpoints are OS, PFS and ORR by RECIST 1.1 and by CA-125 (GCIG criteria). A pre-planned interim analysis was performed by the DSMC in the first 60 patients evaluable for CA-125 response. The analysis met the pre-defined criteria of a CA-125 ORR (GCIG) in the treatment arm at least 10% higher than in the control arm. Study enrolment is ongoing and over 220 patients were enrolled in the US, EU, and Israel. Enrolment of the full sample size of 400 patients is expected to complete by the end of 2021. Clinical trial information: NCT03398655.

APA, Harvard, Vancouver, ISO, and other styles

17

Avery, Neil R. "Thermal evolution of acetylene adsorbed on platinum(111)." Langmuir 4, no. 2 (March 1988): 445–48. http://dx.doi.org/10.1021/la00080a033.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Liu, Z. M., S. A. Costello, B. Roop, S. R. Coon, S. Akhter, and J. M. White. "Surface photochemistry. 6. Methyl bromide on platinum (111)." Journal of Physical Chemistry 93, no. 22 (November 1989): 7681–88. http://dx.doi.org/10.1021/j100359a030.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Jo, Sam K., and J. M. White. "Methyl halide photochemistry on iodine-covered platinum(111)." Journal of the American Chemical Society 115, no. 15 (July 1993): 6934–38. http://dx.doi.org/10.1021/ja00068a061.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Mitchell, G. E., Michael A. Henderson, and J. M. White. "Adsorption and decomposition of trimethylphosphine on platinum(111)." Journal of Physical Chemistry 91, no. 14 (July 1987): 3808–14. http://dx.doi.org/10.1021/j100298a017.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Costello, S. A., B. Roop, Z. M. Liu, and J. M. White. "Photochemistry of methyl bromide adsorbed on platinum(111)." Journal of Physical Chemistry 92, no. 5 (March 1988): 1019–20. http://dx.doi.org/10.1021/j100316a006.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Square, Lynndle C., Christopher J. Arendse, and Theophillus F. G. Muller. "Adsorption of phosphoric acid anions on platinum (111)." Adsorption 23, no. 7-8 (October 13, 2017): 971–81. http://dx.doi.org/10.1007/s10450-017-9912-3.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Blum, L., N. Marzari, and R. Car. "Mechanism of the Hydrogen/Platinum(111) Fuel Cell†." Journal of Physical Chemistry B 108, no. 51 (December 2004): 19670–80. http://dx.doi.org/10.1021/jp047188j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Farkas, A., K. Zalewska-Wierzbicka, C. Bachmann, J. Goritzka, D. Langsdorf, O. Balmes, J. Janek, and H. Over. "High Pressure Carbon Monoxide Oxidation over Platinum (111)." Journal of Physical Chemistry C 117, no. 19 (May 2, 2013): 9932–42. http://dx.doi.org/10.1021/jp401867g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Tachibana, Takeshi, Yoshihiro Yokota, Koji Kobashi, and Mamoru Yoshimoto. "Heteroepitaxial growth of {111}-oriented diamond films on platinum{111}/sapphire{0001} substrates." Journal of Crystal Growth 205, no. 1-2 (August 1999): 163–68. http://dx.doi.org/10.1016/s0022-0248(99)00223-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Arend, Rebecca Christian, Bradley J. Monk, Robert Allen Burger, Thomas J. Herzog, Jonathan A. Ledermann, Kathleen N. Moore, Angeles Alvarez Secord, et al. "Clinical trial in progress: Pivotal study of VB-111 combined with paclitaxel versus paclitaxel for treatment of platinum-resistant ovarian cancer (OVAL, VB-111-701/GOG-3018)." Journal of Clinical Oncology 38, no. 15_suppl (May 20, 2020): TPS6097. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.tps6097.

Full text

Abstract:

TPS6097 Background: Ofranergene obadenovec (VB-111) is a targeted anti-cancer gene therapy with a dual mechanism: a broad antiangiogenic effect and induction of a tumor directed viral immune response. In a phase II trial in platinum resistant ovarian cancer VB-111 in combination with weekly paclitaxel showed a CA-125 response rate (RR) of 58% and median overall survival (OS) of 498 days compared to 172.5 days in the sub-therapeutic dose (p = 0.028). The combination treatment was well tolerated. Favorable outcomes were associated with induction of an immunotherapeutic effect of tumor infiltration with CD-8 T cells. Based on these observations, a phase III randomized controlled trial, VB-111-701/GOG-3018 (OVAL) was initiated in collaboration with the GOG Foundation, Inc. Methods: The OVAL study, NCT03398655, is an international, randomized, double-blind, placebo-controlled, phase III study. Patients with recurrent platinum-resistant epithelial ovarian cancer, who have measurable disease (RECIST 1.1) and were previously treated with up to 5 lines are randomized 1:1 to receive VB-111 (1x1013 VPs) with weekly paclitaxel (80mg/m2), or weekly paclitaxel with placebo. Randomization is stratified by number of prior treatment lines, prior antiangiogenic therapy and platinum refractory disease status. Treatment beyond asymptomatic RECIST progression may continue until progression is confirmed by follow up imaging. The primary endpoints are OS, safety and tolerability. Secondary endpoints include progression free survival, and objective RR by CA-125 (per GCIG criteria) and RECIST 1.1. The sample size calculation of 400 patients (event driven) provides 92% power to detect a difference in survival at the two-sided 5% significance level using the logrank test. A pre-planned interim analysis will take place in Q1 2020 to assess whether the CA-125 RR per GCIG criteria in the treatment arm is sufficiently larger than in the control arm and is comparable to the positive results of the phase II study. Study enrolment is ongoing and over 80 patients were enrolled in the US and Israel. Enrollment expansion to Europe is planned in 2020. Clinical trial information: NCT03398655.

APA, Harvard, Vancouver, ISO, and other styles

27

Schwarz, Kathleen A., Ravishankar Sundararaman, Thomas P. Moffat, and Thomas C. Allison. "Formic acid oxidation on platinum: a simple mechanistic study." Physical Chemistry Chemical Physics 17, no. 32 (2015): 20805–13. http://dx.doi.org/10.1039/c5cp03045e.

Full text

Abstract:

Formic acid oxidation on Pt(111) under electrocatalytic conditions occurs when a formate anion approaches the Pt(111) surface in the CH-down orientation, and barrierlessly releases carbon dioxide as the H binds to the surface.

APA, Harvard, Vancouver, ISO, and other styles

28

Yuan, Chentian, Timo Fuchs, Serhiy Cherevko, Jakub Drnec, Olaf M. Magnussen, and David A. Harrington. "Electrooxidation of Platinum." ECS Meeting Abstracts MA2022-01, no. 55 (July 7, 2022): 2321. http://dx.doi.org/10.1149/ma2022-01552321mtgabs.

Full text

Abstract:

Platinum is an important catalyst widely used in energy conversion and storage, especially in the hydrogen-oxygen polymer electrolyte membrane fuel cell, where it is used at the anode and cathode1. However, potential excursions can lead to surface oxidation and reduction, which restructures the surface and can lower the efficiency of the catalyst and lead to dissolution2. Platinum atoms leave their original lattice sites during oxidation. Surface X-ray diffraction (SXRD) has determined that on Pt(111) the initial stage of Pt extraction is in a place-exchange process, in which the Pt atom moves directly above its original site, which is now occupied by an oxygen atom3. However, on Pt(100) recent work by our team has shown that the initial oxidation gives a “stripe” structure comprising 1D chains of raised Pt and oxygen atoms4. Presented here is an analysis of combined simultaneous SXRD and electrochemistry data for Pt(111) and Pt(100) oxidation in HClO4 and H2SO4. The correlation between the charge transfer and Pt extraction processes is investigated by in-situ cyclic voltammetry, potential step, and potential sweep-hold measurements. The prior structural analysis from a complete set of crystal truncation rods is used find calibration curves for the X-ray intensity of selected anti-Bragg reflections as a function of the coverages θPE of different types of extracted Pt atoms. Integration of charge during electrochemical measurements was converted to electrons passed per surface Pt atoms, to give a notional “electron coverage” θe. In this way, simultaneous measurement of intensity with current during the selected potential program can be converted to θe vs θPE curves. The slopes of these curves are compared with suggested stoichiometric reactions, based on the known SXRD-determined structures. There is some uncertainty insofar as SXRD cannot distinguish O from OH, but we are able to estimate Pt oxidation states. On Pt(111), the electron-transfer and Pt extraction coverage ratios vary with sweep rate, indicating that the rates of adsorption and extraction are kinetically determined and changing during the first oxidation peak. On Pt(100), the stripe structure and stoichiometry suggest a Pt(II) oxide component in the initial stages. We thank other team members involved in various phases of this work: Natalie Stubb (University of Victoria), Valentin Briega-Martos, Daniel Sandbeck (Forschungszentrum Jülich GmbH), Martin Ruge, Ole Fehrs (Kiel University), Federico Calle-Vallejo (Universistat de Barcelona), and the ID31 beamline staff at ESRF. Financial support from NSERC and DFG is appreciated. Reference R. Stamenkovic, D. Strmcnik, P. P. Lopes, N. M. Markovic, Energy and fuels from electrochemical interfaces, Nature materials, 16 (2017) 57-69. J. Sandbeck, O. Brummel, K. J. Mayrhofer, J. Libuda, I. Katsounaros, S. Cherevko, Dissolution of platinum single crystals in acidic medium, ChemPhysChem, 20 (2019) 2997. Drnec, M. Ruge, F. Reikowski, B. Rahn, F. Carlà, R. Felici, J. Stettner, O.M. Magnussen, D.A. Harrington, Initial stages of Pt(111) Electrooxidation: Dynamic and Structural Studies by Surface X-ray Diffraction, Electrochim. Acta, 224 (2017) 220-227. Fuchs, J. Drnec, F. Calle-Vallejo, N. Stubb, D. J. Sandbeck, M. Ruge, S. Cherevko, D. A. Harrington, O. M. Magnussen, Structure dependency of the atomic-scale mechanisms of platinum electro-oxidation and dissolution, Nature Catalysis, 3 (2020) 754-761.

APA, Harvard, Vancouver, ISO, and other styles

29

Cohen, Yael Chava, Suzanne T. Berlin, Michael J. Birrer, Susana M. Campos, Tamar Rachmilewitz Minei, Dror Harats, and Richard T. Penson. "Ofranergene obadenovec (VB-111) in platinum resistant ovarian cancer: with an immunotherapeutic effect." Journal of Clinical Oncology 37, no. 15_suppl (May 20, 2019): 5542. http://dx.doi.org/10.1200/jco.2019.37.15_suppl.5542.

Full text

Abstract:

5542 Background: VB-111 is a targeted anti-cancer gene therapy with a dual mechanism: anti angiogenic/vascular disruption and induction of an anti-tumor directed immune response. We report final results of a phase I/II study of VB-111 in combination with paclitaxel in patients with platinum-resistant ovarian cancer. Methods: Study NCT01711970 was a prospective, open label, dose escalating study assessing combination treatment of VB-111 Q8W and weekly Paclitaxel. In the phase I part of the study patients were treated with escalating doses of intravenous VB-111 and Paclitaxel. In phase 2 patients were treated with therapeutic doses of VB-111 1x1013 Viral Particles and paclitaxel 80mg/m2. Assessments included safety, overall survival (OS), PFS, tumor response (CA-125 and RECIST) and histopathology. Results: 21 patients with recurrent platinum-resistant ovarian cancer were enrolled and treated in 2 US sites. Patients received a mean of 2.3 ±1.8 repeat doses of VB-111. 17/21 received the therapeutic dose. Median age was 65 (41-79) with a median of 3 (1-4) prior lines of therapy. Half of the subjects were Platinum refractory, and half were previously treated with antiangiogenics. No DLTs were observed. VB-111 was well tolerated and was associated with generally mild flu-like symptoms. In the therapeutic dose cohort, a 58% CA-125 GCIG response rate was seen in evaluable patients including durable responses, and responses in patients with platinum refractory disease and post anti-angiogenic failure . The median OS was 498 days in patients treated with Therapeutic Dose compared to 173 days in Sub-therapueutic dose (p = 0.028). Tumor Specimens taken after treatment demonstrated tumor infiltrated with cytotoxic CD8 T-cells and regions of apoptotic cancer cells. Conclusions: Treatment with VB-111 in combination with weekly Paclitaxel was safe and well tolerated. Favorable tumor responses and overall survival outcomes were associated with induction of an immunotherapeutic effect manifested as tumor infiltration with CD-8 T cells. Encouraging results are the basis for further exploration in the ongoing, placebo controlled, pivotal OVAL study. Clinical trial information: NCT01711970.

APA, Harvard, Vancouver, ISO, and other styles

30

Shintani, Yoshihiro. "Growth of highly (111)-oriented, highly coalesced diamond films on platinum (111) surface: A possibility of heteroepitaxy." Journal of Materials Research 11, no. 12 (December 1996): 2955–56. http://dx.doi.org/10.1557/jmr.1996.0373.

Full text

Abstract:

A highly (111)-oriented, highly coalesced diamond film was grown on platinum (111) surface by microwave plasma chemical vapor deposition (MPCVD). Scanning electron microscopy and x-ray diffraction analyses revealed that the (111) diamond facets were azimuthally oriented epitaxially with respect to the orientation of the Pt(111) domain underneath, with the neighboring facets of diamond being coalesced with each other. The film was confirmed as diamond using Raman spectroscopy.

APA, Harvard, Vancouver, ISO, and other styles

31

Grgur, Branimir, Nenad Markovic, Chriss Lucas, and Philip Ross. "Electrochemical oxidation of carbon monoxide: From platinum single crystals to low temperature fuel cells catalysts. Part I: Carbon monoxide oxidation onto low index platinum single crystals." Journal of the Serbian Chemical Society 66, no. 11-12 (2001): 785–97. http://dx.doi.org/10.2298/jsc0112785g.

Full text

Abstract:

The electrochemical oxidation of carbon monoxide and the interfacial structure of the CO adlayer (COads) on platinum low index single crystals, Pt(111), Pt(100) and two reconstruction of Pt(110), were examined using the rotation disk electrode method in combination with the in situ surface X-ray diffraction scattering technique. The mechanism of CO oxidation is discussed on the basis of the findings that, depending on the potential, two energetic states ofCOads exist on the platinum surfaces. Thus, at lower potentials, weakly bonded states (COads,w) and at higher potentials strongly bonded states (COads,s) are formed. The mechanism of the oxidation of hydrogen-carbon monoxide mixtures is also proposed.

APA, Harvard, Vancouver, ISO, and other styles

32

Wong, Yat Ting, and Roald Hoffmann. "Chemisorption of carbon monoxide on three metal surfaces: nickel(111), palladium(111), and platinum(111): a comparative study." Journal of Physical Chemistry 95, no. 2 (January 1991): 859–67. http://dx.doi.org/10.1021/j100155a069.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Grubb, S. G., A. M. DeSantolo, and R. B. Hall. "Optical second-harmonic generation studies of molecular adsorption on platinum (111) and nickel (111)." Journal of Physical Chemistry 92, no. 6 (March 1988): 1419–25. http://dx.doi.org/10.1021/j100317a011.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Hoshi, Nagahiro, Yusuke Asaumi, Masashi Nakamura, Kosuke Mikita, and Risa Kajiwara. "Structural Effects on the Hydrogen Oxidation Reaction on n(111)−(111) Surfaces of Platinum." Journal of Physical Chemistry C 113, no. 39 (September 9, 2009): 16843–46. http://dx.doi.org/10.1021/jp9076239.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Ragan, Regina, Doug Ohlberg, Jason J. Blackstock, Sehun Kim, and R. Stanley Williams. "Atomic Surface Structure of UHV-Prepared Template-Stripped Platinum and Single-Crystal Platinum(111)." Journal of Physical Chemistry B 108, no. 52 (December 2004): 20187–92. http://dx.doi.org/10.1021/jp0466789.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Richardson, S. J., M. R. Burton, P. A. Staniec, I. S. Nandhakumar, N. J. Terrill, J. M. Elliott, and A. M. Squires. "Aligned platinum nanowire networks from surface-oriented lipid cubic phase templates." Nanoscale 8, no. 5 (2016): 2850–56. http://dx.doi.org/10.1039/c5nr06691c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Zhang, J., M. B. Vukmirovic, K. Sasaki, F. Uribe, and R. R. Adzic. "Platinum monolayer electrocatalysts for oxygen reduction: Effect of substrates, and long-term stability." Journal of the Serbian Chemical Society 70, no. 3 (2005): 513–25. http://dx.doi.org/10.2298/jsc0503513z.

Full text

Abstract:

We describe a novel concept for a Pt monolayer electrocatalyst and present the results of our electrochemical, X-ray absorption spectroscopy, and scanning tunneling microscopy studies. The electrocatalysts were prepared by a new method for depositing Pt monolayers involving the galvanic displacement by Pt of an under potentially deposited Cu monolayer on substrates of Au (111), Ir(111), Pd(111), Rh(111) and Ru(0001) single crylstals, and Pd nanoparticles. The kinetics of O2 reduction showed significant enhancement with Pt monolayers on Pd(111) and Pd nanoparticle surfaces in comparisonwith the reaction on Pt(111) and Pt nanoparticles, respectively. This increase in catalytic activity is attributed partly to the decreased formation of PtOH, as shown by in situ X-ray absorption spectroscopy. The results illustrate that placing a Pt monolayer on a suitable substrate of metal nanoparticles is an attractive way of designing better O2 reduction electrocatalysts with very low Pt contents.

APA, Harvard, Vancouver, ISO, and other styles

38

Bartram, Michael E., R. G. Windham, and B. E. Koel. "Coadsorption of nitrogen dioxide and oxygen on platinum(111)." Langmuir 4, no. 2 (March 1988): 240–46. http://dx.doi.org/10.1021/la00080a001.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Heikkinen, Olli, Hugo Pinto, Godhuli Sinha, Sampsa K. Hämäläinen, Jani Sainio, Sven Öberg, Patrick R. Briddon, Adam S. Foster, and Jouko Lahtinen. "Characterization of a Hexagonal Phosphorus Adlayer on Platinum (111)." Journal of Physical Chemistry C 119, no. 22 (May 21, 2015): 12291–97. http://dx.doi.org/10.1021/jp5126816.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Johnson, Allen L., E. L. Muetterties, J. Stohr, and F. Sette. "Chemisorption geometry of pyridine on platinum(111) by NEXAFS." Journal of Physical Chemistry 89, no. 19 (September 1985): 4071–75. http://dx.doi.org/10.1021/j100265a029.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Henderson, Michael A., and J. M. White. "Adsorption and decomposition of dimethyl methylphosphonate on platinum(111)." Journal of the American Chemical Society 110, no. 21 (October 1988): 6939–47. http://dx.doi.org/10.1021/ja00229a002.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Liu, Z. M., X. L. Zhou, D. A. Buchanan, J. Kiss, and J. M. White. "The surface chemistry of vinyl iodide on platinum(111)." Journal of the American Chemical Society 114, no. 6 (March 1992): 2031–39. http://dx.doi.org/10.1021/ja00032a016.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Komanicky, Vladimir, and W. Ronald Fawcett. "Fabrication of an annealable platinum (111) single crystal ultramicroelectrode." Journal of Electroanalytical Chemistry 556 (September 2003): 109–15. http://dx.doi.org/10.1016/s0022-0728(03)00336-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Jiang, L. Q., Armen Avoyan, Bruce E. Koel, and John L. Falconer. "Methylcyclohexane-to-benzene conversion over potassium-promoted platinum(111)." Journal of the American Chemical Society 115, no. 25 (December 1993): 12106–10. http://dx.doi.org/10.1021/ja00078a056.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Kyuno, Kentaro, and Gert Ehrlich. "Diffusion and dissociation of platinum clusters on Pt(111)." Surface Science 437, no. 1-2 (August 1999): 29–37. http://dx.doi.org/10.1016/s0039-6028(99)00659-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Ernst, K. H., and K. Christmann. "The interaction of glycine with a platinum (111) surface." Surface Science 224, no. 1-3 (December 1989): 277–310. http://dx.doi.org/10.1016/0039-6028(89)90916-3.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Ernst, K. H., and K. Christmann. "The interaction of glycine with a platinum (111) surface." Surface Science Letters 224, no. 1-3 (December 1989): A628. http://dx.doi.org/10.1016/0167-2584(89)90160-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Dong, C. Z., S. M. Shivaprasad, K. ‐J Song, and T. E. Madey. "Platinum‐induced morphology and reactivity changes on W(111)." Journal of Chemical Physics 99, no. 11 (December 1993): 9172–81. http://dx.doi.org/10.1063/1.465532.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Gölzhäuser, Armin, and Gert Ehrlich. "Direct Observation of Platinum Atoms on Pt(111) Clusters." Zeitschrift für Physikalische Chemie 202, Part_1_2 (January 1997): 59–74. http://dx.doi.org/10.1524/zpch.1997.202.part_1_2.059.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Wang, Zhanzhong, Quanyu Suo, Caixia Zhang, Zhanli Chai, and Xiaojing Wang. "Solvent-controlled platinum nanocrystals with a high growth rate along 〈100〉 to 〈111〉 and enhanced electro-activity in the methanol oxidation reaction." RSC Advances 6, no. 92 (2016): 89098–102. http://dx.doi.org/10.1039/c6ra18171f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!