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Full Quantum Dynamics of Complex Che...

Zhang, Luhao.

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Full Quantum Dynamics of Complex Chemical System--Modelling Excited State Proton Transfer.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Full Quantum Dynamics of Complex Chemical System--Modelling Excited State Proton Transfer./
作者:	Zhang, Luhao.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2023,
面頁冊數:	115 p.
附註:	Source: Dissertations Abstracts International, Volume: 84-10, Section: B.
Contained By:	Dissertations Abstracts International84-10B.
標題:	Physical chemistry. -
電子資源:	https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30310031
ISBN:	9798379403690

Full Quantum Dynamics of Complex Chemical System--Modelling Excited State Proton Transfer.
Zhang, Luhao.

Full Quantum Dynamics of Complex Chemical System--Modelling Excited State Proton Transfer. - Ann Arbor : ProQuest Dissertations & Theses, 2023 - 115 p.

Source: Dissertations Abstracts International, Volume: 84-10, Section: B.

Thesis (Ph.D.)--Princeton University, 2023.

This item is not available from ProQuest Dissertations & Theses.

Non-equilibrium dynamics of chemical and biological systems generally take place in chemical reactions and biological functions. Proton transfer is fundamental and ubiquitous whose mechanisms provide basic insights for more complex processes. Excited state proton transfer reaction (ESIPT) is the ideal model system for studying proton transfer mechanism because its dynamics can be controlled and tracked by light. As the general challenge faced in studying non-equilibrium proton transfer, complex quantum interactions among multiple degrees of freedom causes that the field does not have well-established theory at present. In this dissertation, we combine complex system methodology and theory of open quantum system to model ESIPT and provide mechanistic understanding. We construct an effective Hamiltonian of open quantum dynamics to simulate the quantum interplay of electron, proton, molecular skeleton, solvent, and light. It precisely quantifies the time-resolved spectroscopies of two single-site molecules, which reveals the deterministic motion and interaction could be protonic-electronic transition induced by proton-electron vibronic coupling, rather than semiclassical skeleton deformation assisting ballistic proton delivery as thought before. The vibronic coupling interaction can cause resonant electron-proton oscillation that determines the oscillatory pattern of time-resolved spectroscopy. The same model framework is applied to a double-site molecule, which suggests that the experimental symmetry-dependent isotope effect could be from quantum interference between two reaction channels. The next step will be prediction and validation to confirm these novel mechanisms and keep on developing ESIPT effective Hamiltonian which can be useful to the broader field of condensed phase chemical dynamics.{A0}

ISBN: 9798379403690Subjects--Topical Terms:

1981412
Physical chemistry.
Subjects--Index Terms:

Quantum dynamics

Full Quantum Dynamics of Complex Chemical System--Modelling Excited State Proton Transfer.
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245 1 0 $a Full Quantum Dynamics of Complex Chemical System--Modelling Excited State Proton Transfer.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2023
300 $a 115 p.
500 $a Source: Dissertations Abstracts International, Volume: 84-10, Section: B.
500 $a Advisor: Scholes, Gregory D.
502 $a Thesis (Ph.D.)--Princeton University, 2023.
506 $a This item is not available from ProQuest Dissertations & Theses.
506 $a This item must not be sold to any third party vendors.
520 $a Non-equilibrium dynamics of chemical and biological systems generally take place in chemical reactions and biological functions. Proton transfer is fundamental and ubiquitous whose mechanisms provide basic insights for more complex processes. Excited state proton transfer reaction (ESIPT) is the ideal model system for studying proton transfer mechanism because its dynamics can be controlled and tracked by light. As the general challenge faced in studying non-equilibrium proton transfer, complex quantum interactions among multiple degrees of freedom causes that the field does not have well-established theory at present. In this dissertation, we combine complex system methodology and theory of open quantum system to model ESIPT and provide mechanistic understanding. We construct an effective Hamiltonian of open quantum dynamics to simulate the quantum interplay of electron, proton, molecular skeleton, solvent, and light. It precisely quantifies the time-resolved spectroscopies of two single-site molecules, which reveals the deterministic motion and interaction could be protonic-electronic transition induced by proton-electron vibronic coupling, rather than semiclassical skeleton deformation assisting ballistic proton delivery as thought before. The vibronic coupling interaction can cause resonant electron-proton oscillation that determines the oscillatory pattern of time-resolved spectroscopy. The same model framework is applied to a double-site molecule, which suggests that the experimental symmetry-dependent isotope effect could be from quantum interference between two reaction channels. The next step will be prediction and validation to confirm these novel mechanisms and keep on developing ESIPT effective Hamiltonian which can be useful to the broader field of condensed phase chemical dynamics.{A0}
590 $a School code: 0181.
650 4 $a Physical chemistry. $3 1981412
650 4 $a Chemistry. $3 516420
650 4 $a Physics. $3 516296
653 $a Quantum dynamics
653 $a Biological systems
653 $a Protonic-electronic transition
653 $a Time-resolved spectroscopies
653 $a Non-equilibrium
690 $a 0494
690 $a 0605
690 $a 0485
710 2 $a Princeton University. $b Chemistry. $3 2094742
773 0 $t Dissertations Abstracts International $g 84-10B.
790 $a 0181
791 $a Ph.D.
792 $a 2023
793 $a English
856 4 0 $u https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30310031