A Message from the Chair, Robin Hochstrasser
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Herent Control of Condensed Matter with Attosecond Precision Hiroyuki Katsuki, Nobuyuki Takei, Christian Sommer, and Kenji Ohmori Acc
CURRICULUM VITAE Christian Sommer, postdoc @ Max Planck Institute for the Science of Light Dr. Christian Sommer Personal Data Date of Birth: 22. 01. 1980 Place of Birth: Elmshorn, Germany Marital Status: Single Citizenship: Germany Contact details Werner-von-Siemens-Str. 10 91052 Erlangen +49 (0) 173 6817144 [email protected] [email protected] Google scholar link: google scholar ResearchGate profile: ResearchGate Competencies Laser Spectroscopy, Laser Technology (UV, VIS, IR Lase), Optics, Optical Detectors, and Optical Measurement Methods Microwave Technology, Microwave synthesizer and waveguides Designing Analog and Digital Electronics Data Acquisition and Data Analysis, Presentation of Data Computer Simulations, Machine learning and Software Skills Writing Scientific Publications and Reports Reviewing Scientific Publications Talks and Presentations Command of Languages Mass Spectrometry High- and Ultrahigh Vacuum Technology and Cryogenic Technology Application of High-voltage Devices Work Experience 01/2017 - present Postdoctoral Researcher (theoretical physics) Max Planck Institute for the Science of Light in the group of Dr. Claudiu Genes, Erlangen, Germany. Projects Analytic calculations in the field of open quantum systems with the focus on collective effects, Cavity QED with molecules and cooling of optomechanical systems Machine learning (Reinforcement learning) for controlling stochastic dynamical systems . Emphases and Professional Activities Performing computer simulations Writing scientific publications -
Distance Dependence of Photoinduced Long-Range Electron Transfer in Zinc/Ruthenium-Modified Myoglobins
J. Am. Chem. SOC.1988, 110, 435-439 435 Distance Dependence of Photoinduced Long-Range Electron Transfer in Zinc/Ruthenium-Modified Myoglobins Andrew W. Axup, Michael Albin, Stephen L. Mayo, Robert J. Crutchley,' and Harry B. Gray* Contribution No. 7588 from the Arthur Amos Noyes Laboratory, California Institute of Technology, Pasadena, California 91 125. Received May 8, I987 Abstract: An experimental investigation of the distance dependence of long-range electron transfer in zinc/ruthenium-modified myoglobins has been performed. The modified proteins were prepared by substitution of zinc mesoporphyrin IX diacid (ZnP) for the heme in each of four previously characterized pentaammineruthenium(II1) (a5Ru; a = NH,) derivatives of sperm whale myoglobin (Mb): a5Ru(His-48)Mb, aSRu(His-12)Mb, a5Ru(His-l 16)Mb, a5Ru(His-81)Mb. Electron transfer from the ZnP triplet excited state (,ZnP*) to Ru3+, 3ZnP*-Ru3t -+ ZnP+-Ru2+ (AEo - 0.8 V) was measured by time-resolved transient absorption spectroscopy: rate constants (kf)are 7.0 X lo4 (His-48), 1.0 X IO2 (His-12), 8.9 X 10' (His-1 16), and 8.5 X IO' (His-81) s-' at 25 OC. Activation enthalpies calculated from the temperature dependences of the electron-transfer rates over the range 5-40 OC are 1.7 i 1.6 (His-48), 4.7 i 0.9 (His-12), 5.4 i 0.4 (His-116), and 5.6 i 2.5 (His-81) kcal mol-'. Electron-transfer distances (d = closest ZnP edge to a5Ru(His) edge; angstroms) were calculated to fall in the following ranges: His-48, 11.8-16.6; His-12, 21.5-22.3; His-116, 19.8-20.4; His-81, 18.8-19.3. -
The Electronic Structure of Biomolecular Self-Assembled Monolayers" (2012)
University of South Florida Scholar Commons Graduate Theses and Dissertations Graduate School January 2012 The lecE tronic Structure of Biomolecular Self- Assembled Monolayers Matthaeus Anton Wolak University of South Florida, [email protected] Follow this and additional works at: http://scholarcommons.usf.edu/etd Part of the American Studies Commons, Electrical and Computer Engineering Commons, and the Materials Science and Engineering Commons Scholar Commons Citation Wolak, Matthaeus Anton, "The Electronic Structure of Biomolecular Self-Assembled Monolayers" (2012). Graduate Theses and Dissertations. http://scholarcommons.usf.edu/etd/4258 This Dissertation is brought to you for free and open access by the Graduate School at Scholar Commons. It has been accepted for inclusion in Graduate Theses and Dissertations by an authorized administrator of Scholar Commons. For more information, please contact [email protected]. The Electronic Structure of Biomolecular Self-Assembled Monolayers by Matthaeus Wolak A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy Department of Electrical Engineering College of Engineering University of South Florida Major Professor: Rudy Schlaf, Ph.D. Vinay Gupta, Ph.D. Li-June Ming, Ph.D. Arash Takshi, Ph.D. Jing Wang, Ph.D. Date of Approval: June 13, 2012 Keywords: peptide nucleic acid, tetraphenylporphyrin, work function, charge injection barrier, interface dipole, XPS Copyright © 2012, Matthaeus Wolak DEDICATION I dedicate my dissertation to my girlfriend Emily Helmrich, and my parents Margarete and Anton Wolak, who supported me throughout the process and always had the right words of encouragement for me. I am very grateful to you and will always appreciate all that you have done for me. -
COHERENCE Book of Abstracts
1 SPONSORS The Marie Curie Initial Training Network network COHERENCE: Cooperativity in Highly Excited Rydberg Ensembles { Control and Entanglement Patronato de la Alhambra y Generalife 2 LOCAL ORGANIZING COMMITTEE Rosario Gonz´alez-F´erez • Universidad de Granada, Spain Javier Aguilera Fern´andez • Universidad de Granada, Spain SCIENTIFIC ADVISORY COMMITTEE Charles S. Adams • Durham University, UK Thomas Pohl • Max-Planck-Institut f¨urPhysik komplexer Systeme, Dresden, Germany Guido Pupillo • Laboratoire de Physique Quantique, CNRS, Strasbourg, France Shannon Whitlock • Ruprecht-Karl University Heidelberg, Germany YEA MEETING ORGANIZING COMMITTEE Javier Aguilera Fern´andez • Universidad de Granada, Spain Vladislav Gavryusev • Universit¨atHeidelberg, Germany Henning Labuhn • Laboratoire Charles Fabry, Institut d'Optique, CNRS, France Andrew Wade • Aarhus Universitet, Aarhus, Denmark 3 Practical information The YEA meeting and Idea Factory will be held at the "Carmen de la Victoria" • (Cuesta del Chapiz 9, Granada 18010) The Ultracold Rydberg Atoms Workshop will be held at the Escuela de Estu- • dios Arabes "Casas del Chapiz" (Cuesta del Chapiz 22, Granada 18010) Lunches and coffee breaks will take place at the "Carmen de la Victoria" • The conference dinner will take place on Thursday September 12, at 20.30 at: • Hotel AC Palacio de Santa Paula in Calle Gran Via de Col´on31 The main locations are displayed on the map below, A Escuela de Estudios Arabes,´ B Carmen de la Victoria and C Hotel AC Palacio de Santa Paula. Wireless in the workshop -
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A Symphony of Charge Transfer Theory, Conductive DNA Junction Modeling and Chemical Library Design by Yuqi Zhang Department of Chemistry Duke University Date:_______________________ Approved: ___________________________ David Beratan, Supervisor ___________________________ Katherine Franz ___________________________ Jie Liu ___________________________ Weitao Yang Dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry in the Graduate School of Duke University 2016 i v ABSTRACT A Symphony of Charge Transfer Theory, Conductive DNA Junction Modeling and Chemical Library Design by Yuqi Zhang Department of Chemistry Duke University Date:_______________________ Approved: ___________________________ David Beratan, Supervisor ___________________________ Katherine Franz ___________________________ Jie Liu ___________________________ Weitao Yang An abstract of a dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry in the Graduate School of Duke University 2016 i v Copyright by Yuqi Zhang 2016 Abstract Biological electron transfer (ET) reactions are typically described in the framework of coherent two-state electron tunneling or multi-step hopping. Yet, these ET reactions may involve multiple redox cofactors in van der Waals contact with each other and with vibronic broadenings on the same scale as the energy gaps among the species. In this regime, fluctuations of the molecule and its medium can produce transient energy level matching among multiple electronic states. This transient degeneracy, or flickering electronic resonance among states, is found to support coherent (ballistic) charge transfer. Importantly, ET rates arising from a flickering resonance (FR) mechanism will decay exponentially with distance because the probability of energy matching multiple states is multiplicative. -
Missing Rung Problem in Vibrational Ladder Climbing
Missing Rung Problem in Vibrational Ladder Climbing Takahiro Horiba, Soichi Shirai, and Hirotoshi Hirai∗ Toyota Central Research and Development Labs., Inc., 41-1, Yokomichi, Nagakute, Aichi 480-1192, Japan (Dated: August 18, 2021) We observed vanishing of the transition dipole moment, interrupting vibrational ladder climbing (VLC) in molecular systems. We clarified the mechanism of this phenomenon and present a method to use an additional chirped pulse to preserve the VLC. To show the effectiveness of our method, we conducted wavepacket dynamics simulations for LiH dissociations with chirped pulses. The results indicate that the efficiency of LiH dissociation is significantly improved by our method compared to conventional methods. We also revealed the quantum interference effect behind the excitation process of VLC. Controlling molecular reactions as desired is one of such as plasma systems [21] and superconducting circuits the ultimate goals of chemistry. Compared to conven- [22]. The excitation condition proposed by Duan et al. tional macroscopic reaction control methods using tem- and the characterization parameters proposed by Fried- perature and pressure, proposed methods that directly land et al. depend on the physical properties of the sys- control the quantum state of molecules using the electric tem such as the potential energy surface (PES) and the field of a laser are expected to achieve dramatically im- dipole function. Thereby, these properties determine the proved efficiency and selectivity of reactions [1–3]. Such characteristic of the VLC. However, most of the theo- techniques, first proposed by Brumer and Shapiro in the retical treatments were based on simple model functions 1980s [1], are called “coherent control”, and with the ad- of these properties such as Morse potentials and linear vent of femtosecond pulsed lasers and the development dipole moments [12, 15, 23–25]. -
Nonadiabatic Control for Quantum Information Processing And
UNIVERSITY OF CALGARY Nonadiabatic Control for Quantum Information Processing and Biological Electron Transfer by Nathan S. Babcock A DISSERTATION SUBMITTED TO THE FACULTY OF GRADUATE STUDIES IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY DEPARTMENT OF PHYSICS AND ASTRONOMY CALGARY, ALBERTA April, 2015 c Nathan S. Babcock 2015 Abstract In this Thesis, I investigate two disparate topics in the fields of quantum information processing and macromolecular biochemistry, inter-related by the underlying physics of nonadiabatic electronic transitions (i.e., the breakdown of the Born-Oppenheimer ap- proximation). The main body of the Thesis is divided into two Parts. In Part I, I describe my proposal for a two-qubit quantum logic gate to be implemented based on qubits stored using the total orbital angular momentum states of ultracold neutral atoms. I carry out numerical analyses to evaluate gate fidelity over a range of gate speeds, and I derive a simple criterion to ensure adiabatic gate operation. I propose a scheme to significantly improve the gate's fidelity without decreasing its speed. I contribute to the development of a \loophole-free" Bell inequality test based on the use of this gate by carrying out an order-of-magnitude feasibility analysis to assess whether the test is viable given realistic technological limitations. In Part II, I investigate electron transfer reaction experiments performed on native and mutant forms of the MADH{amicyanin redox complex derived from P. denitrificans. I implement molecular dynamics simulations of native and mutant forms of the solvated MADH{amicyanin complex. I analyze the resulting nuclear coordinate trajectories, both geometrically and in terms of electronic redox coupling. -
FEATURE: JSPS Prize 2007
Japan Society for the Promotion of Science FEATURE: JSPS Prize R T O P I C S ● JSPS Prize ....................................................................................................................................... 2 ● JSPS Office Opens in Beijing ................................................................................................... 6 ● Messages from JSPS Overseas Office Directors ............................................................... 7 ● ERC Launch Conference Attended by JSPS President .................................................. 8 No.20 ● Seminar Held with India’s DST ............................................................................................... 8 ● Trilateral Workshop Held between Japan, China and Korea ...................................... 9 2007 ● Tenth Meeting Held of Japan-India Science Council ..................................................... 9 Summer ● AAAS Symposium Supported by San Francisco Office ................................................. 9 ● First JUNBA General Assembly .............................................................................................. 10 ● Stockholm Office Holds Sixth Science Forum .................................................................. 10 ● Second Conference for Bridging Japan and the UK ...................................................... 10 ● Science Dialogue ........................................................................................................................ 11 ● Message from Former JSPS Fellow -
Attosecond Control of Restoration of Electronic Structure Symmetry
PHYSICAL REVIEW LETTERS 121, 173201 (2018) Attosecond Control of Restoration of Electronic Structure Symmetry † ChunMei Liu,1 Jörn Manz,1,2,3,* Kenji Ohmori,4,5, Christian Sommer,4,5,6 Nobuyuki Takei,4,5 Jean Christophe Tremblay,1 and Yichi Zhang2,3,4 1Freie Universität Berlin, Institut für Chemie und Biochemie, 14195 Berlin, Germany 2State Key Laboratory of Quantum Optics and Quantum Optics Devices, Institute of Laser Spectroscopy, Shanxi University, Taiyuan 030006, China 3Collaborative Innovation Center of Extreme Optics, Shanxi University, Taiyuan 030006, China 4Institute for Molecular Science, National Institutes of Natural Sciences, Myodaiji, Okazaki 444-8585, Japan 5SOKENDAI (The Graduate University of Advanced Studies), Myodaiji, Okazaki 444-8585, Japan 6Max-Planck-Institut für die Physik des Lichts, 91058 Erlangen, Germany (Received 23 March 2018; published 25 October 2018) Laser pulses can break the electronic structure symmetry of atoms and molecules by preparing a superposition of states with different irreducible representations. Here, we discover the reverse process, symmetry restoration, by means of two circularly polarized laser pulses. The laser pulse for symmetry restoration is designed as a copy of the pulse for symmetry breaking. Symmetry restoration is achieved if the time delay is chosen such that the superposed states have the same phases at the temporal center. This condition must be satisfied with a precision of a few attoseconds. Numerical simulations are presented for 87 the C6H6 molecule and Rb atom. The experimental feasibility of symmetry restoration is demonstrated by means of high-contrast time-dependent Ramsey interferometry of the 87Rb atom. DOI: 10.1103/PhysRevLett.121.173201 The purpose of this Letter is to show that well-designed system is in a quasi-field-free environment—at initial laser pulses can not only break (see, e.g., Refs. -
Ground and Electronic Excited States from Pairing Matrix Fluctuation and Particle-Particle Random Phase Approximation
Ground and Electronic Excited States from Pairing Matrix Fluctuation and Particle-Particle Random Phase Approximation by Yang Yang Department of Chemistry Duke University Date: Approved: Weitao Yang, Supervisor David Beratan Patrick Charbonneau Harold Baranger Dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry in the Graduate School of Duke University 2016 Abstract Ground and Electronic Excited States from Pairing Matrix Fluctuation and Particle-Particle Random Phase Approximation by Yang Yang Department of Chemistry Duke University Date: Approved: Weitao Yang, Supervisor David Beratan Patrick Charbonneau Harold Baranger An abstract of a dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry in the Graduate School of Duke University 2016 Copyright c 2016 by Yang Yang All rights reserved except the rights granted by the Creative Commons Attribution-Noncommercial Licence Abstract The accurate description of ground and electronic excited states is an important and challenging topic in quantum chemistry. The pairing matrix fluctuation, as a counter- part of the density fluctuation, is applied to this topic. From the pairing matrix fluc- tuation, the exact electron correlation energy as well as two electron addition/removal energies can be extracted. Therefore, both ground state and excited states energies can be obtained and they are in principle exact with a complete knowledge of the pairing matrix fluctuation. In practice, considering the exact pairing matrix fluctua- tion is unknown, we adopt its simple approximation | the particle-particle random phase approximation (pp-RPA) | for ground and excited states calculations. -
4 Th APS Workshop on Opportunities in Biological Physics
THE BIOLOGICAL PHYSICIST The Newsletter of the Division of Biological Physics of the American Physical Society Vol 6 No 6 February 2007 DIVISION OF BIOLOGICAL PHYSICS EXECUTIVE COMMITTEE Chair In this Issue Marilyn Gunner [email protected] Immediate Past Chair Peter Jung MARCH MEETING SPECIAL EDITION! [email protected] Chair-Elect Dean Astumian PRL HIGHLIGHTS………………………………………..…..….....1 [email protected] PRE HIGHLIGHTS………………………………………..….……..6 Vice-Chair James Glazier [email protected] SPECIAL MARCH MEETING FEATURES Secretary/Treasurer Opportunities in Biological Physics Workshop………….10 Shirley Chan Downtown Denver Map………………………….………….28 [email protected] DBP Schedule for March Meeting……..........……..............29 APS Councilor Robert Eisenberg [email protected] Members-at-Large: Lois Pollack This special March Meeting edition of the DBP [email protected] newsletter brings you PRE and PRL Highlights, and a Stephen Quake handy compilation of all the DBP sessions at the [email protected] March Meeting, as well as a map of downtown Denver Stephen J. Hagen [email protected] and full details about the Opportunities in Biological Chao Tang Physics Workshop. Find more March Meeting details, [email protected] including the Program Scheduler & the “Epitome”, at Réka Albert [email protected] http://www.aps.org/meetings/march/index.cfm. Brian Salzberg [email protected] Don’t forget to attend the DBP Business Meeting on Newsletter Editor th Sonya Bahar Tuesday March 6 at 5:45 pm in Room 405 of the [email protected] Colorado Convention Center! Website Coordinator Andrea Markelz See you in Denver! [email protected] Website Assistant -- SB Lois Pollack [email protected] 1 PRL HIGHLIGHTS Soft Matter, Biological, & Entropy-Driven Formation of the Gyroid Inter-disciplinary Physics Articles from Cubic Phase L. -
Report of the Committee on Proposal Evaluation for Allocation of Supercomputing Time for the Study of Molecular Dynamics: Fifth Round
This PDF is available from The National Academies Press at http://www.nap.edu/catalog.php?record_id=18961 Report of the Committee on Proposal Evaluation for Allocation of Supercomputing Time for the Study of Molecular Dynamics: Fifth Round ISBN Committee on Proposal Evaluation for Allocation of Supercomputing Time 978-0-309-31301-8 for the Study of Molecular Dynamics, Fifth Round; Board on Life Sciences; Division on Earth and Life Studies; National Research Council 20 pages 8.5 x 11 2014 Visit the National Academies Press online and register for... Instant access to free PDF downloads of titles from the NATIONAL ACADEMY OF SCIENCES NATIONAL ACADEMY OF ENGINEERING INSTITUTE OF MEDICINE NATIONAL RESEARCH COUNCIL 10% off print titles Custom notification of new releases in your field of interest Special offers and discounts Distribution, posting, or copying of this PDF is strictly prohibited without written permission of the National Academies Press. Unless otherwise indicated, all materials in this PDF are copyrighted by the National Academy of Sciences. Request reprint permission for this book Copyright © National Academy of Sciences. All rights reserved. Report of the Committee on Proposal Evaluation for Allocation of Supercomputing Time for the Study of Molecular Dynamics: Fifth Round Report of the Committee on Proposal Evaluation for Allocation of Supercomputing Time for the Study of Molecular Dynamics, Fifth Round Committee on Proposal Evaluation for Allocation of Supercomputing Time for the Study of Molecular Dynamics, Fifth Round Board on Life Sciences Division on Earth and Life Studies Copyright © National Academy of Sciences. All rights reserved. Report of the Committee on Proposal Evaluation for Allocation of Supercomputing Time for the Study of Molecular Dynamics: Fifth Round Copyright © National Academy of Sciences.