Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/141866
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dc.contributor.authorZhang, Zhengyangen_US
dc.contributor.authorHuerta-Viga, Adrianaen_US
dc.contributor.authorTan, Howe-Siangen_US
dc.date.accessioned2020-06-11T06:02:21Z-
dc.date.available2020-06-11T06:02:21Z-
dc.date.issued2018-
dc.identifier.citationZhang, Z., Huerta-Viga, A., & Tan, H.-S. (2018). Two-dimensional electronic-Raman spectroscopy. Optics letters, 43(4), 939-942. doi:10.1364/OL.43.000939en_US
dc.identifier.issn0146-9592en_US
dc.identifier.urihttps://hdl.handle.net/10356/141866-
dc.description.abstractWe present a new technique, two-dimensional electronic-Raman spectroscopy (2DER), which combines femtosecond stimulated Raman spectroscopy and a pulse-shaper-assisted 2D spectroscopic scheme for the actinic pump. The 2DER spectrum presents the initial actinic excitation wavelength with nanometer spectral resolution in the first axis and the detected stimulated Raman spectra in the second axis. We measured the correlation of the electronic and vibrational states in the photosynthetic accessory pigment β-carotene and reveal its photoexcited state manifold.en_US
dc.description.sponsorshipMOE (Min. of Education, S’pore)en_US
dc.language.isoenen_US
dc.relation.ispartofOptics lettersen_US
dc.rights© 2018 Optical Society of America. All rights reserved.en_US
dc.subjectScience::Chemistryen_US
dc.titleTwo-dimensional electronic-Raman spectroscopyen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.1364/OL.43.000939-
dc.identifier.pmid29444032-
dc.identifier.scopus2-s2.0-85042078547-
dc.identifier.issue4en_US
dc.identifier.volume43en_US
dc.identifier.spage939en_US
dc.identifier.epage942en_US
dc.subject.keywordsUltrafast Spectroscopyen_US
dc.subject.keywordsSpectroscopyen_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
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