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One Step at a Time: Enhancing Fluorescence-Detected Two-Dimensional Electronic Spectroscopy
One Step at a Time: Enhancing Fluorescence-Detected Two-Dimensional Electronic Spectroscopy
Detailed Information
- 자료유형
- 학위논문 서양
- 최종처리일시
- 20250211152956
- ISBN
- 9798384043379
- DDC
- 530
- 서명/저자
- One Step at a Time: Enhancing Fluorescence-Detected Two-Dimensional Electronic Spectroscopy
- 발행사항
- [Sl] : University of Michigan, 2024
- 발행사항
- Ann Arbor : ProQuest Dissertations & Theses, 2024
- 형태사항
- 144 p
- 주기사항
- Source: Dissertations Abstracts International, Volume: 86-03, Section: B.
- 주기사항
- Advisor: Ogilvie, Jennifer.
- 학위논문주기
- Thesis (Ph.D.)--University of Michigan, 2024.
- 초록/해제
- 요약Photosynthesis is the foundational biological process that converts light into chemical energy. The initial steps of photosynthesis achieve near-unity quantum efficiency in converting excitation energy to charge-separated states essential for fueling cellular processes. The underlying mechanisms have proven to be an inspiring model to design photovoltaics. Recent advancements in femtosecond multidimensional spectroscopy have revolutionized our ability to examine the ultrafast energy conversion processes, providing unprecedented insights into the intricate dynamics that occur within femtoseconds of light absorption. This thesis details the development and optimization of linear and two-dimensional electronic spectroscopic (2DES) techniques designed to broaden the bandwidth applicability of these high-resolution methods.Fluorescence-detected 2DES (F-2DES) is a powerful tool offering high temporal and spectral resolution while allowing for spatially resolved measurements. Previous implementations of F-2DES used a step-scanning approach, requiring typical acquisition times of minutes for a single F-2DES spectrum. To further optimize this technique, I present work on developing a phase-modulation rapid-scanning fluorescence-detected 2DES (F-2DES) methodology utilizing continuous scanning and digital lock-in acquisition. The approach enables interferometric tracking of the time delays to allow for correction of spectral phase distortions and accurate phasing of the data. We demonstrate the significant improvement of acquisition time by measuring IR140 in DMSO, retrieving the linear fluorescence excitation spectrum, and the rephasing, non-rephasing, and absorptive fluorescence-detected two-dimensional electronic spectra with a six second acquisition time.Our initial implementation of F-2DES had limited spectral bandwidth due to the use of acousto-optic modulators (AOMs) for phase modulation. This motivated my subsequent work incorporating broadband light to rapid-scanning F-2DES. We circumvent the bandwidth limitations of the method by generating the continuum after the phase-modulation, demonstrating that the phase modulation is preserved in continuum generation, enabling the rest of the phase-modulated rapid-scanning method. I present a proof-of-principle of this broadband phase-modulated rapid-scanning method through linear absorption and fluorescence excitation measurements. The resulting spectra of laser dyes and various biological samples match closely with a commercial linear absorption spectrometer. We also maintain the benefits of the phase-modulated rapid-scanning method of low acquisition times with 2.5 s generating comparable spectra to the commercial spectrometer with acquisition times on the order of minutes. We finally propose that this linear broadband experiment can be scaled to the complete phase-modulated rapid-scanning F-2DES experiment.
- 일반주제명
- Physics
- 일반주제명
- Optics
- 일반주제명
- Biophysics
- 키워드
- Photosynthesis
- 키워드
- Chemical energy
- 기타저자
- University of Michigan Physics
- 기본자료저록
- Dissertations Abstracts International. 86-03B.
- 전자적 위치 및 접속
- 로그인 후 원문을 볼 수 있습니다.
MARC
008250123s2024 us c eng d■001000017164389
■00520250211152956
■006m o d
■007cr#unu||||||||
■020 ▼a9798384043379
■035 ▼a(MiAaPQ)AAI31631203
■035 ▼a(MiAaPQ)umichrackham005655
■040 ▼aMiAaPQ▼cMiAaPQ
■0820 ▼a530
■1001 ▼aSessa, Francesco.
■24510▼aOne Step at a Time: Enhancing Fluorescence-Detected Two-Dimensional Electronic Spectroscopy
■260 ▼a[Sl]▼bUniversity of Michigan▼c2024
■260 1▼aAnn Arbor▼bProQuest Dissertations & Theses▼c2024
■300 ▼a144 p
■500 ▼aSource: Dissertations Abstracts International, Volume: 86-03, Section: B.
■500 ▼aAdvisor: Ogilvie, Jennifer.
■5021 ▼aThesis (Ph.D.)--University of Michigan, 2024.
■520 ▼aPhotosynthesis is the foundational biological process that converts light into chemical energy. The initial steps of photosynthesis achieve near-unity quantum efficiency in converting excitation energy to charge-separated states essential for fueling cellular processes. The underlying mechanisms have proven to be an inspiring model to design photovoltaics. Recent advancements in femtosecond multidimensional spectroscopy have revolutionized our ability to examine the ultrafast energy conversion processes, providing unprecedented insights into the intricate dynamics that occur within femtoseconds of light absorption. This thesis details the development and optimization of linear and two-dimensional electronic spectroscopic (2DES) techniques designed to broaden the bandwidth applicability of these high-resolution methods.Fluorescence-detected 2DES (F-2DES) is a powerful tool offering high temporal and spectral resolution while allowing for spatially resolved measurements. Previous implementations of F-2DES used a step-scanning approach, requiring typical acquisition times of minutes for a single F-2DES spectrum. To further optimize this technique, I present work on developing a phase-modulation rapid-scanning fluorescence-detected 2DES (F-2DES) methodology utilizing continuous scanning and digital lock-in acquisition. The approach enables interferometric tracking of the time delays to allow for correction of spectral phase distortions and accurate phasing of the data. We demonstrate the significant improvement of acquisition time by measuring IR140 in DMSO, retrieving the linear fluorescence excitation spectrum, and the rephasing, non-rephasing, and absorptive fluorescence-detected two-dimensional electronic spectra with a six second acquisition time.Our initial implementation of F-2DES had limited spectral bandwidth due to the use of acousto-optic modulators (AOMs) for phase modulation. This motivated my subsequent work incorporating broadband light to rapid-scanning F-2DES. We circumvent the bandwidth limitations of the method by generating the continuum after the phase-modulation, demonstrating that the phase modulation is preserved in continuum generation, enabling the rest of the phase-modulated rapid-scanning method. I present a proof-of-principle of this broadband phase-modulated rapid-scanning method through linear absorption and fluorescence excitation measurements. The resulting spectra of laser dyes and various biological samples match closely with a commercial linear absorption spectrometer. We also maintain the benefits of the phase-modulated rapid-scanning method of low acquisition times with 2.5 s generating comparable spectra to the commercial spectrometer with acquisition times on the order of minutes. We finally propose that this linear broadband experiment can be scaled to the complete phase-modulated rapid-scanning F-2DES experiment.
■590 ▼aSchool code: 0127.
■650 4▼aPhysics
■650 4▼aOptics
■650 4▼aBiophysics
■653 ▼aMultidimensional spectroscopy
■653 ▼aPhotosynthesis
■653 ▼aChemical energy
■653 ▼aDimensional electronic spectroscopic fluorescence
■653 ▼aBandwidth limitations
■690 ▼a0605
■690 ▼a0786
■690 ▼a0752
■71020▼aUniversity of Michigan▼bPhysics.
■7730 ▼tDissertations Abstracts International▼g86-03B.
■790 ▼a0127
■791 ▼aPh.D.
■792 ▼a2024
■793 ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17164389▼nKERIS▼z이 자료의 원문은 한국교육학술정보원에서 제공합니다.
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