R
Renske M. van der Veen
Researcher at University of Illinois at Urbana–Champaign
Publications - 38
Citations - 1096
Renske M. van der Veen is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Absorption spectroscopy & Excited state. The author has an hindex of 14, co-authored 33 publications receiving 967 citations. Previous affiliations of Renske M. van der Veen include California Institute of Technology & École Polytechnique Fédérale de Lausanne.
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Journal ArticleDOI
Subparticle Ultrafast Spectrum Imaging in 4D Electron Microscopy
TL;DR: The development of subparticle imaging with space, time, and energy resolutions of nanometers, femtoseconds, and millielectron volts is reported, opening the door to various applications in elemental analysis as well as mapping of interfaces and plasmonics.
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Single-nanoparticle phase transitions visualized by four-dimensional electron microscopy
TL;DR: By introducing a small aperture in the microscope, it was possible to follow the phase transition and the associated structural dynamics within a single particle and has potential applications in other nanosystems and those that undergo (bio)chemical transformations.
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Vibrational relaxation and intersystem crossing of binuclear metal complexes in solution
TL;DR: The vibrational relaxation and coherence decay processes are established, and it is demonstrated that PtPOP represents a clear example of a harmonic oscillator that does not comply with the optical Bloch description due to very efficient coherence transfer between vibronic levels.
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Structural determination of a photochemically active diplatinum molecule by time-resolved EXAFS spectroscopy.
Renske M. van der Veen,Renske M. van der Veen,Christopher J. Milne,Amal El Nahhas,Frederico A. Lima,Van-Thai Pham,Jonathan Best,Julia A. Weinstein,Camelia N. Borca,Rafael Abela,Christian Bressler,Majed Chergui +11 more
TL;DR: The strengthening of the Pt-Pt interaction is accompanied by a weakening of the ligand coordination bonds, resulting in an elongation of the platinum-ligand bond that is determined for the first time by time-resolved X-ray absorption spectroscopy.
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A high-repetition rate scheme for synchrotron-based picosecond laser pump/x-ray probe experiments on chemical and biological systems in solution
Frederico A. Lima,Christopher J. Milne,Dimali C.V. Amarasinghe,Dimali C.V. Amarasinghe,M. H. Rittmann-Frank,Renske M. van der Veen,Renske M. van der Veen,Marco Reinhard,Van-Thai Pham,Van-Thai Pham,Susanne Karlsson,Steven L. Johnson,Daniel Grolimund,Camelia N. Borca,Thomas Huthwelker,Markus Janousch,Frank van Mourik,Rafael Abela,Majed Chergui +18 more
TL;DR: An order of magnitude increase in the signal-to-noise of time-resolved XAS of molecular systems in solution is demonstrated, which makes it possible to investigate highly dilute samples at concentrations approaching physiological conditions for biological systems.