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Resonant Photoemission Spectroscopy as a Probe for Ultrafast Electron Transfer in Organic Semiconductors.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Resonant Photoemission Spectroscopy as a Probe for Ultrafast Electron Transfer in Organic Semiconductors./
作者:	Duong, Vincent.
面頁冊數:	1 online resource (238 pages)
附註:	Source: Dissertations Abstracts International, Volume: 80-08, Section: B.
Contained By:	Dissertations Abstracts International80-08B.
標題:	Physical chemistry. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10936005click for full text (PQDT)
ISBN:	9780438853331

Resonant Photoemission Spectroscopy as a Probe for Ultrafast Electron Transfer in Organic Semiconductors.
Duong, Vincent.

Resonant Photoemission Spectroscopy as a Probe for Ultrafast Electron Transfer in Organic Semiconductors. - 1 online resource (238 pages)

Source: Dissertations Abstracts International, Volume: 80-08, Section: B.

Thesis (Ph.D.)--University of California, Santa Cruz, 2018.

Includes bibliographical references

Electron transfer (ET) is a fundamental process in chemical and physical systems. This thesis is concerned with ET in organic semiconductor systems, which have prominent applications as low cost solar cells and miniaturized, next generation electronics. Within these contexts, one of the emerging research questions concerns ET on the femtosecond (informally, the ultrafast) timescale. While prior results have connected the ultrafast timescales to the majority of delocalized electrons in a system are generated on these femtosecond timescales, an accurate understanding of these dynamics has proven elusive. This is because the popular probe of electron dynamics, optical pump-probe experiments, can struggle with such short timescales. However, Resonant Photoemission Spectroscopy (RPES), a variant of X-ray absorption and photoemission spectroscopy, can probe ET rates at such ultrafast timescales (0.5 fs to 50 fs) with the added benefit of elemental selectivity and surface sensitivity. This technique is a stead-state experiment based on comparing the electron transfer rate to the core-hole decay rate, which is well known and generally unperturbed in low-Z atoms prevalent in organic semiconductors. The applications of this work concern both the fundamental quantum mechanics at interfaces and the nature of the core-hole in the X-ray excited state as well as more applied work concerning the rational design of future organic semiconductors. This thesis leverages RPES to explore the question of ET at interfaces in the context of organic semiconductors. The first study involves between Copper(II) phthalocyanine (CuPc), a model planar organometallic compound, and its fluorinated analog Copper(II) hexadecafluorophthalocyanine (F16) and examines the role of local electronic environment on ET rates. Fluorine was chosen as the fluorine atom is highly electronegative and thus a large perturbation to the electronic structure while simultaneously being very small and thus having a minor impact on the atomic structure. Additionally, fluorination of organic semiconductors is a common tool in modifying the electronic structure by lowering the HOMO and LUMO energies, reducing the degradative oxidation processes, and often yields p-type semiconductors. Experimental RPES results show electron transfer on the nitrogen K-edge to be faster for CuPc over F16 by a factor of two while electron transfer on the carbon K-edge showed F16 to be faster than CuPc. DFT results show a almost no modification of the electronic structure but a large shift in the energy levels of the fluorine bound carbons. An examination of the X-ray diffraction pattern and the corresponding literature results in two distinct crystal structures. This implies the difference in ET is connected to the in-column stacking and neighboring column stacking. The second study explores the size dependence of a molecule by examining a series of 4-,5-, and 6- molecule long thiophene molecules. The role of molecular size has been throughly explored before, though typically in the context of polymer systems and not in the context of ultrafast dynamics. The thiophene monomer is a well-known baseline in the field with sexithiophene (6 monomers) being one of the most studied small molecules and the functionalized polymer molecule, poly(3-hexylthiophene-2,5-diyl), as one of the most studied polymers. The initial hypothesis argued the larger molecules would have more delocalized electrons which would, in turn, screen the core-hole from the excited electrons. This would have implied easier delocalization (faster rates) as the molecule grew in size. The alternative hypothesis reasoned that the core-hole was a strong localizing potential and the ET time would be constant as a function molecule length. Instead, the results indicated that 5-thiophene molecule had the fastest delocalization time, beyond the range of the RPES technique. The rational for this result is inconclusive but may be related to the odd number of monomer units, thus implying some type of odd-even effect in conjugation length. The third study involves a series of functionalized thiophenol molecules bound to a gold surface. The molecular system of choice is a fluorinated thiophenol and the experiment involves excitations on the fluorine K-edge. The premise of the experiment involves the electrons excited from the fluorine 1s orbital and, possibly, delocalizing across the benzene structure through the sulfur bond and into the gold substrate/continuum. These experiments are strongly reminiscent of break-junction STM experiments popularized in the molecular electronics community. In the first experiment, the location of the fluorine atom was moved from being meta-oriented with respect to the sulfur atom to being para-oriented relative to the sulfur atom. This experiment probed the destructive interference properties of meta-oriented electron transfer to contrast with the constructive interference properties of the para-oriented molecule. The results show a comparable electron transfer rate between the two molecule, implying an inability to probe the constructive/destructive properties via the RPE process. (Abstract shortened by ProQuest.).

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023

Mode of access: World Wide Web

ISBN: 9780438853331Subjects--Topical Terms:

1981412
Physical chemistry.
Subjects--Index Terms:

Molecular electronicsIndex Terms--Genre/Form:

542853
Electronic books.

Resonant Photoemission Spectroscopy as a Probe for Ultrafast Electron Transfer in Organic Semiconductors.
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520 $a Electron transfer (ET) is a fundamental process in chemical and physical systems. This thesis is concerned with ET in organic semiconductor systems, which have prominent applications as low cost solar cells and miniaturized, next generation electronics. Within these contexts, one of the emerging research questions concerns ET on the femtosecond (informally, the ultrafast) timescale. While prior results have connected the ultrafast timescales to the majority of delocalized electrons in a system are generated on these femtosecond timescales, an accurate understanding of these dynamics has proven elusive. This is because the popular probe of electron dynamics, optical pump-probe experiments, can struggle with such short timescales. However, Resonant Photoemission Spectroscopy (RPES), a variant of X-ray absorption and photoemission spectroscopy, can probe ET rates at such ultrafast timescales (0.5 fs to 50 fs) with the added benefit of elemental selectivity and surface sensitivity. This technique is a stead-state experiment based on comparing the electron transfer rate to the core-hole decay rate, which is well known and generally unperturbed in low-Z atoms prevalent in organic semiconductors. The applications of this work concern both the fundamental quantum mechanics at interfaces and the nature of the core-hole in the X-ray excited state as well as more applied work concerning the rational design of future organic semiconductors. This thesis leverages RPES to explore the question of ET at interfaces in the context of organic semiconductors. The first study involves between Copper(II) phthalocyanine (CuPc), a model planar organometallic compound, and its fluorinated analog Copper(II) hexadecafluorophthalocyanine (F16) and examines the role of local electronic environment on ET rates. Fluorine was chosen as the fluorine atom is highly electronegative and thus a large perturbation to the electronic structure while simultaneously being very small and thus having a minor impact on the atomic structure. Additionally, fluorination of organic semiconductors is a common tool in modifying the electronic structure by lowering the HOMO and LUMO energies, reducing the degradative oxidation processes, and often yields p-type semiconductors. Experimental RPES results show electron transfer on the nitrogen K-edge to be faster for CuPc over F16 by a factor of two while electron transfer on the carbon K-edge showed F16 to be faster than CuPc. DFT results show a almost no modification of the electronic structure but a large shift in the energy levels of the fluorine bound carbons. An examination of the X-ray diffraction pattern and the corresponding literature results in two distinct crystal structures. This implies the difference in ET is connected to the in-column stacking and neighboring column stacking. The second study explores the size dependence of a molecule by examining a series of 4-,5-, and 6- molecule long thiophene molecules. The role of molecular size has been throughly explored before, though typically in the context of polymer systems and not in the context of ultrafast dynamics. The thiophene monomer is a well-known baseline in the field with sexithiophene (6 monomers) being one of the most studied small molecules and the functionalized polymer molecule, poly(3-hexylthiophene-2,5-diyl), as one of the most studied polymers. The initial hypothesis argued the larger molecules would have more delocalized electrons which would, in turn, screen the core-hole from the excited electrons. This would have implied easier delocalization (faster rates) as the molecule grew in size. The alternative hypothesis reasoned that the core-hole was a strong localizing potential and the ET time would be constant as a function molecule length. Instead, the results indicated that 5-thiophene molecule had the fastest delocalization time, beyond the range of the RPES technique. The rational for this result is inconclusive but may be related to the odd number of monomer units, thus implying some type of odd-even effect in conjugation length. The third study involves a series of functionalized thiophenol molecules bound to a gold surface. The molecular system of choice is a fluorinated thiophenol and the experiment involves excitations on the fluorine K-edge. The premise of the experiment involves the electrons excited from the fluorine 1s orbital and, possibly, delocalizing across the benzene structure through the sulfur bond and into the gold substrate/continuum. These experiments are strongly reminiscent of break-junction STM experiments popularized in the molecular electronics community. In the first experiment, the location of the fluorine atom was moved from being meta-oriented with respect to the sulfur atom to being para-oriented relative to the sulfur atom. This experiment probed the destructive interference properties of meta-oriented electron transfer to contrast with the constructive interference properties of the para-oriented molecule. The results show a comparable electron transfer rate between the two molecule, implying an inability to probe the constructive/destructive properties via the RPE process. (Abstract shortened by ProQuest.).
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