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Driven by Light: An Ultrafast Look into the Bright Future of Photosensitizers
Driven by Light: An Ultrafast Look into the Bright Future of Photosensitizers
Driven by Light: An Ultrafast Look into the Bright Future of Photosensitizers

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211151147
ISBN  
9798383164808
DDC  
540
저자명  
Schaffner, Jacob William.
서명/저자  
Driven by Light: An Ultrafast Look into the Bright Future of Photosensitizers
발행사항  
[Sl] : University of Minnesota, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
359 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-12, Section: B.
주기사항  
Advisor: Blank, David A.
학위논문주기  
Thesis (Ph.D.)--University of Minnesota, 2024.
초록/해제  
요약This thesis investigates various strong light-absorbing molecules that have potential applications in furthering our progress into replacing fossil fuels with clean energy resources and remediating harmful chemicals in the environment. The research presented in this thesis employs a range of spectroscopic techniques, complemented with computational predictions, to characterize the light absorption and excited state dynamics of newly developed chromophores that have shown promise in these various applications. Chapter 3 investigates a BODIPY-fullerene dyad designed to be used in organic photovoltaics as a triplet sensitizer to form longer-lived excitons. This triplet sensitization occurs via a ping-pong energy transfer mechanism between the BODIPY and fullerene, resulting in a long-lived BODIPY triplet (1 µs). Chapters 4 and 5 investigate the MB-DIPY chromophore that could potentially displace fullerene as a strong and more versatile electron acceptor in organic photovoltaics. In Chapter 4, the redox potentials and photophysics of four MB-DIPY analogs are explored. The MB-DIPYs had comparable reduction potentials to fullerene and demonstrated efficient intersystem crossing to form long-lived triplet states (10 µs). In Chapter 5, the MB-DIPY is functionalized with ferrocene, a strong electron donor, and demonstrated sub-ps charge-transfer from the ferrocene to the MB-DIPY followedby charge recombination in 12 ps. Chapters 6 and 7 investigate the Rh-Ga and Co-Ga heterobimetallic photocatalyststhat can access challenging bonds via a photoredox mechanism. The excited state nature of these photocatalysts is first explored in Chapter 6. The results were consistent with the naked anionic catalyst being the active participant in the photocatalytic cycle. Chapter 7 investigates the reactivity of the photocatalysts with a chloroadamantanesubstrate. The results suggested that the substrate binds to the anionic rhodium photocatalyst and that the photocatalytic reactivity is not diffusion-limited. In contrast, the anionic cobalt catalyst was converted into the chlorinated precatalyst upon the addition of the substrate, demonstrating that the chemical reactivity of the rhodium and cobalt photocatalysts differ with this substrate.
일반주제명  
Chemistry
일반주제명  
Physical chemistry
일반주제명  
Analytical chemistry
일반주제명  
Optics
키워드  
Heterobimetallic catalysts
키워드  
Manitoba azadipyrromethenes
키워드  
Photocatalysis
키워드  
Photovoltaics
키워드  
Spectroscopy
기타저자  
University of Minnesota Chemistry
기본자료저록  
Dissertations Abstracts International. 85-12B.
전자적 위치 및 접속  
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MARC

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■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a540
■1001  ▼aSchaffner,  Jacob  William.
■24510▼aDriven  by  Light:  An  Ultrafast  Look  into  the  Bright  Future  of  Photosensitizers
■260    ▼a[Sl]▼bUniversity  of  Minnesota▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a359  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-12,  Section:  B.
■500    ▼aAdvisor:  Blank,  David  A.
■5021  ▼aThesis  (Ph.D.)--University  of  Minnesota,  2024.
■520    ▼aThis  thesis  investigates  various  strong  light-absorbing  molecules  that  have  potential  applications  in  furthering  our  progress  into  replacing  fossil  fuels  with  clean  energy  resources  and  remediating  harmful  chemicals  in  the  environment.  The  research  presented  in  this  thesis  employs  a  range  of  spectroscopic  techniques,  complemented  with  computational  predictions,  to  characterize  the  light  absorption  and  excited  state  dynamics  of  newly  developed  chromophores  that  have  shown  promise  in  these  various  applications.  Chapter  3  investigates  a  BODIPY-fullerene  dyad  designed  to  be  used  in  organic  photovoltaics  as  a  triplet  sensitizer  to  form  longer-lived  excitons.  This  triplet  sensitization  occurs  via  a  ping-pong  energy  transfer  mechanism  between  the  BODIPY  and  fullerene,  resulting  in  a  long-lived  BODIPY  triplet  (1  µs).  Chapters  4  and  5  investigate  the  MB-DIPY  chromophore  that  could  potentially  displace  fullerene  as  a  strong  and  more  versatile  electron  acceptor  in  organic  photovoltaics.  In  Chapter  4,  the  redox  potentials  and  photophysics  of  four  MB-DIPY  analogs  are  explored.  The  MB-DIPYs  had  comparable  reduction  potentials  to  fullerene  and  demonstrated  efficient  intersystem  crossing  to  form  long-lived  triplet  states  (10  µs).  In  Chapter  5,  the  MB-DIPY  is  functionalized  with  ferrocene,  a  strong  electron  donor,  and  demonstrated  sub-ps  charge-transfer  from  the  ferrocene  to  the  MB-DIPY  followedby  charge  recombination  in  12  ps.  Chapters  6  and  7  investigate  the  Rh-Ga  and  Co-Ga  heterobimetallic  photocatalyststhat  can  access  challenging  bonds  via  a  photoredox  mechanism.  The  excited  state  nature  of  these  photocatalysts  is  first  explored  in  Chapter  6.  The  results  were  consistent  with  the  naked  anionic  catalyst  being  the  active  participant  in  the  photocatalytic  cycle.  Chapter  7  investigates  the  reactivity  of  the  photocatalysts  with  a  chloroadamantanesubstrate.  The  results  suggested  that  the  substrate  binds  to  the  anionic  rhodium  photocatalyst  and  that  the  photocatalytic  reactivity  is  not  diffusion-limited.  In  contrast,  the  anionic  cobalt  catalyst  was  converted  into  the  chlorinated  precatalyst  upon  the  addition  of  the  substrate,  demonstrating  that  the  chemical  reactivity  of  the  rhodium  and  cobalt  photocatalysts  differ  with  this  substrate.
■590    ▼aSchool  code:  0130.
■650  4▼aChemistry
■650  4▼aPhysical  chemistry
■650  4▼aAnalytical  chemistry
■650  4▼aOptics
■653    ▼aHeterobimetallic  catalysts
■653    ▼aManitoba  azadipyrromethenes
■653    ▼aPhotocatalysis
■653    ▼aPhotovoltaics
■653    ▼aSpectroscopy
■690    ▼a0485
■690    ▼a0494
■690    ▼a0486
■690    ▼a0752
■71020▼aUniversity  of  Minnesota▼bChemistry.
■7730  ▼tDissertations  Abstracts  International▼g85-12B.
■790    ▼a0130
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17160993▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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