Helen Fielding | |
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Born | Helen H. Fielding |
Alma mater | University of Cambridge (BA) University of Oxford (DPhil) |
Awards |
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Scientific career | |
Fields | Physical chemistry |
Institutions | University College London King's College London University of Amsterdam National Physical Laboratory |
Thesis | The Stark effect in atomic and molecular Rydberg states (1992) |
Doctoral advisor | Timothy Softley [1] |
Website | www |
Helen H. Fielding FRSC FInstP CPhys CChem is a Professor of physical chemistry at University College London (UCL). [2] She focuses on ultrafast transient spectroscopy of protein chromophores and molecules. She was the first woman to win the Royal Society of Chemistry (RSC) Harrison-Meldola Memorial Prize (1996) and Marlow Award (2001).
Fielding studied the Natural Sciences Tripos at the University of Cambridge. She began her PhD at the University of Cambridge, working with Timothy Softley, but moved with him to the University of Oxford where they studied excited quantum states using photoelectron spectroscopy. [1] [3] [4] She was awarded her Doctor of Philosophy degree in 1992. [1] [5]
Fielding was a scientist at the National Physical Laboratory from 1992 to 1993. In 1993 she joined the University of Amsterdam as a postdoctoral fellow, working with Ben van Linden van den Heuvell. Here she worked on Rydberg wave packets in coulombic and magnetic fields. [6]
Fielding was appointed a lecturer at King's College London in 1994 after only 18 months of postdoctoral work. [7] She was the first woman to be awarded the Harrison-Meldola Memorial Prize in 1996. [8] She is interested in how to excite electron functions coherently, generating a wave packets with a localised probability distribution. [7] Electron movement occurs on the attosecond timescale, making them impossible to image using conventional laser technology. [9] Instead, Fielding employs femtosecond laser pulses to excite electrons to these highly excited Rydberg states. In these excited states, electrons behave both as a particle and a wave, and can be controlled using its wave-like characteristics. [9] She has become one of few worldwide experts in the field. [9] She is primarily interested in materials such as small organic chromophores and photoactivated peptides. [10]
She made the first observation of a wave packet in a Rydberg molecule in 2000. [11] This observation made her interested in coherent control, looking to exploit the phase of a rotating Rydberg molecule to manipulate the dynamics of chemical systems. [7] She explored the decay pathways of the Rydberg molecule NO. [7] Fielding used the wavelength and phase of the laser light to select whether NO decays via ionisation or dissociation. [7] One decay route will be the result of constructive interference and the other the result of destructive interference. [7] This study represented a breakthrough in the field; where light of a precise phase could be used to control molecular dynamics. [7] [12] She became interested in how the optical phase corresponds to the electronic and molecular phase, with a particular focus on the attosecond. [7]
Fielding was made an EPSRC advanced research fellow in 2001, and was the first woman to be awarded the Royal Society of Chemistry Marlow Medal. [8] [13] In 2003 Fielding moved to University College London, where she leads a large laser laboratory. [7] Her recent research has focussed on the dynamics of excited states formed during the absorption of ultraviolet light. [10] [14] She has studied the competition between internal conversion and electron detachment in protein chromophores. [15]
She has worked extensively on ultrafast chemical biology in the gas phase. [16] [17] [18] Fielding developed time-resolved photoelectron spectroscopy to study the relaxation dynamics of photoexcited molecules. [10] She has investigated the intramolecular dynamics of vibrationally and electronically excited benzene, and demonstrated new electron transfer pathways in pyrrole dimers. [19] [20]
Fielding has two children. [16]
Femtochemistry is the area of physical chemistry that studies chemical reactions on extremely short timescales in order to study the very act of atoms within molecules (reactants) rearranging themselves to form new molecules (products). In a 1988 issue of the journal Science, Ahmed Hassan Zewail published an article using this term for the first time, stating "Real-time femtochemistry, that is, chemistry on the femtosecond timescale...". Later in 1999, Zewail received the Nobel Prize in Chemistry for his pioneering work in this field showing that it is possible to see how atoms in a molecule move during a chemical reaction with flashes of laser light.
In physics and physical chemistry, time-resolved spectroscopy is the study of dynamic processes in materials or chemical compounds by means of spectroscopic techniques. Most often, processes are studied after the illumination of a material occurs, but in principle, the technique can be applied to any process that leads to a change in properties of a material. With the help of pulsed lasers, it is possible to study processes that occur on time scales as short as 10−16 seconds. All time-resolved spectra are suitable to be analyzed using the two-dimensional correlation method for a correlation map between the peaks.
Photoemission spectroscopy (PES), also known as photoelectron spectroscopy, refers to energy measurement of electrons emitted from solids, gases or liquids by the photoelectric effect, in order to determine the binding energies of electrons in the substance. The term refers to various techniques, depending on whether the ionization energy is provided by X-ray, XUV or UV photons. Regardless of the incident photon beam, however, all photoelectron spectroscopy revolves around the general theme of surface analysis by measuring the ejected electrons.
Rydberg ionization spectroscopy is a spectroscopy technique in which multiple photons are absorbed by an atom causing the removal of an electron to form an ion.
Ultrafast laser spectroscopy is a category of spectroscopic techniques using ultrashort pulse lasers for the study of dynamics on extremely short time scales. Different methods are used to examine the dynamics of charge carriers, atoms, and molecules. Many different procedures have been developed spanning different time scales and photon energy ranges; some common methods are listed below.
The Rydberg states of an atom or molecule are electronically excited states with energies that follow the Rydberg formula as they converge on an ionic state with an ionization energy. Although the Rydberg formula was developed to describe atomic energy levels, it has been used to describe many other systems that have electronic structure roughly similar to atomic hydrogen. In general, at sufficiently high principal quantum numbers, an excited electron-ionic core system will have the general character of a hydrogenic system and the energy levels will follow the Rydberg formula. Rydberg states have energies converging on the energy of the ion. The ionization energy threshold is the energy required to completely liberate an electron from the ionic core of an atom or molecule. In practice, a Rydberg wave packet is created by a laser pulse on a hydrogenic atom and thus populates a superposition of Rydberg states. Modern investigations using pump-probe experiments show molecular pathways – e.g. dissociation of (NO)2 – via these special states.
Ultraviolet photoelectron spectroscopy (UPS) refers to the measurement of kinetic energy spectra of photoelectrons emitted by molecules that have absorbed ultraviolet photons, in order to determine molecular orbital energies in the valence region.
Photoelectrochemical processes are processes in photoelectrochemistry; they usually involve transforming light into other forms of energy. These processes apply to photochemistry, optically pumped lasers, sensitized solar cells, luminescence, and photochromism.
Photoelectron photoion coincidence spectroscopy (PEPICO) is a combination of photoionization mass spectrometry and photoelectron spectroscopy. It is largely based on the photoelectric effect. Free molecules from a gas-phase sample are ionized by incident vacuum ultraviolet (VUV) radiation. In the ensuing photoionization, a cation and a photoelectron are formed for each sample molecule. The mass of the photoion is determined by time-of-flight mass spectrometry, whereas, in current setups, photoelectrons are typically detected by velocity map imaging. Electron times-of-flight are three orders of magnitude smaller than those of ions, which allows electron detection to be used as a time stamp for the ionization event, starting the clock for the ion time-of-flight analysis. In contrast with pulsed experiments, such as REMPI, in which the light pulse must act as the time stamp, this allows to use continuous light sources, e.g. a discharge lamp or a synchrotron light source. No more than several ion–electron pairs are present simultaneously in the instrument, and the electron–ion pairs belonging to a single photoionization event can be identified and detected in delayed coincidence.
Philip H. Bucksbaum is an American atomic physicist, the Marguerite Blake Wilbur Professor in Natural Science in the Departments of Physics, Applied Physics, and Photon Science at Stanford University and the SLAC National Accelerator Laboratory. He also directs the Stanford PULSE Institute.
Time-resolved two-photon photoelectron (2PPE) spectroscopy is a time-resolved spectroscopy technique which is used to study electronic structure and electronic excitations at surfaces. The technique utilizes femtosecond to picosecond laser pulses in order to first photoexcite an electron. After a time delay, the excited electron is photoemitted into a free electron state by a second pulse. The kinetic energy and the emission angle of the photoelectron are measured in an electron energy analyzer. To facilitate investigations on the population and relaxation pathways of the excitation, this measurement is performed at different time delays.
The magnesium argide ion, MgAr+ is an ion composed of one ionised magnesium atom, Mg+ and an argon atom. It is important in inductively coupled plasma mass spectrometry and in the study of the field around the magnesium ion. The ionization potential of magnesium is lower than the first excitation state of argon, so the positive charge in MgAr+ will reside on the magnesium atom. Neutral MgAr molecules can also exist in an excited state.
Albert Stolow is a Canadian physicist. He is the Canada Research Chair in Molecular Photonics, full professor of chemistry & biomolecular sciences and of physics, and a member of the Ottawa Institute for Systems Biology at the University of Ottawa. He is the founder and an ongoing member of the Molecular Photonics Group at the National Research Council of Canada. He is adjunct professor of Chemistry and of Physics at Queen's University in Kingston, and a Graduate Faculty Scholar in the department of physics, University of Central Florida and a Fellow of the Max-Planck-uOttawa Centre for Extreme and Quantum Photonics. In 2008, he was elected a Fellow in the American Physical Society, nominated by its Division of Chemical Physics in 2008, for contributions to ultrafast laser science as applied to molecular physics, including time-resolved studies of non-adiabatic dynamics in excited molecules, non-perturbative quantum control of molecular dynamics, and dynamics of polyatomic molecules in strong laser fields. In 2008, Stolow won the Keith Laidler Award of the Canadian Society for Chemistry, for a distinguished contribution to the field of physical chemistry, recognizing early career achievement. In 2009, he was elected a Fellow of the Optical Society of America for the application of ultrafast optical techniques to molecular dynamics and control, in particular, studies of molecules in strong laser fields and the development of new methods of optical quantum control. In 2013, he was awarded the Queen Elizabeth II Diamond Jubilee Medal (Canada). In 2017, Stolow was awarded the Earle K. Plyler Prize for Molecular Spectroscopy and Dynamics of the American Physical Society for the development of methods for probing and controlling ultrafast dynamics in polyatomic molecules, including time-resolved photoelectron spectroscopy and imaging, strong field molecular ionization, and dynamic Stark quantum control. In 2018, Stolow was awarded the John C. Polanyi Award of the Canadian Society for Chemistry “for excellence by a scientist carrying out research in Canada in physical, theoretical or computational chemistry or chemical physics”. In 2020, he became Chair of the Division of Chemical Physics of the American Physical Society. His group's research interests include ultrafast molecular dynamics and quantum control, time-resolved photoelectron spectroscopy and imaging, strong field & attosecond physics of polyatomic molecules, and coherent non-linear optical microscopy of live cells/tissues, materials and geological samples. In 2020, Stolow launched a major new high power ultrafast laser facility at the University of Ottawa producing high energy, phase-controlled few-cycle pulses of 2 micron wavelength at 10 kHz repetition rate. These are used for High Harmonic Generation to produce bright ultrafast Soft X-ray pulses for a new Ultrafast Xray Science Laboratory.
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Hrvoje Petek is a Croatian-born American physicist and the Richard King Mellon Professor of Physics and Astronomy, at the University of Pittsburgh, where he is also a professor of chemistry.
Tamar Seideman is the Dow Chemical Company Professor of Chemistry and Professor of Physics at Northwestern University. She specialises in coherence spectroscopies and coherent control in isolated molecules and dissipative media as well as in ultrafast nanoplasmonics, current-driven phenomena in nanoelectronics and mathematical models.
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