소장자료
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| 005 | 20250522163624▲ | ||
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| 008 | 250123s2024 us ||||||||||||||c||eng d▲ | ||
| 020 | ▼a9798383045138▲ | ||
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| 040 | ▼aMiAaPQ▼cMiAaPQ▼d221016▲ | ||
| 082 | 0 | ▼a541▲ | |
| 100 | 1 | ▼aLiu, Yufeng.▲ | |
| 245 | 1 | 0 | ▼aPhotoinduced Transfer of Spin-Polarized Charges at Semiconductor Interfaces▼h[electronic resource].▲ |
| 260 | ▼a[S.l.]: ▼bColumbia University. ▼c2024▲ | ||
| 260 | 1 | ▼aAnn Arbor : ▼bProQuest Dissertations & Theses, ▼c2024▲ | |
| 300 | ▼a1 online resource(111 p.)▲ | ||
| 500 | ▼aSource: Dissertations Abstracts International, Volume: 85-12, Section: B.▲ | ||
| 500 | ▼aAdvisor: Zhu, Xiaoyang.▲ | ||
| 502 | 1 | ▼aThesis (Ph.D.)--Columbia University, 2024.▲ | |
| 520 | ▼aCharge transfer at the organic/inorganic semiconductor interfaces lies at the heart of interfacial photochemistry. While decades of research have shaped the current understanding that interfacial charge transfer depends crucially on energetic driving force and electronic coupling, much less is known about the role played by the spin degree of freedom. In particular, it is not clear how spin states evolve during the charge transfer process. With the advent of group 6 transition metal dichalcogenides (TMDC), a class of two-dimensional layered materials which permits the optical generation of spin-polarized electron-hole pairs in the monolayer limit, we now have the opportunity to investigate if charge transfer at an organic/inorganic interface could enable the transfer of spin polarization. Using time-resolved Faraday rotation and transient absorption spectroscopy, it is found in the MoSe2/H2Pc and C60/WS2 heterostructures that the photoinduced hole transfer from MoSe2 to H2Pc and electron transfer from WS2 to C60 results in spin polarization lifetimes one order of magnitude longer than that of a monolayer. In the WS2/MoSe2/H2Pc heterostructure, the addition of a WS2 monolayer drives the dissociation of electron-hole pairs bound at the MoSe2/H2Pc interface and leads to the observation of nanosecond-long spin polarization at room temperature. These findings evidence the photoinduced transfer of spin polarization, a mechanism which could potentially be exploited to enhance the efficiency and selectivity of photochemical reactions involving angular momentum change, and may be generalized to other organic/inorganic interfaces composed of crystalline semiconductors with spin-momentum locking.▲ | ||
| 590 | ▼aSchool code: 0054.▲ | ||
| 650 | 4 | ▼aPhysical chemistry.▲ | |
| 650 | 4 | ▼aMaterials science.▲ | |
| 650 | 4 | ▼aCondensed matter physics.▲ | |
| 650 | 4 | ▼aOptics.▲ | |
| 653 | ▼aCharge transfer▲ | ||
| 653 | ▼aHeterostructures▲ | ||
| 653 | ▼aOptical spectroscopy▲ | ||
| 653 | ▼aOrganic semiconductors▲ | ||
| 653 | ▼aSpin polarization▲ | ||
| 653 | ▼aTransition metal dichalcogenides▲ | ||
| 690 | ▼a0494▲ | ||
| 690 | ▼a0794▲ | ||
| 690 | ▼a0752▲ | ||
| 690 | ▼a0611▲ | ||
| 710 | 2 | 0 | ▼aColumbia University.▼bChemical Physics.▲ |
| 773 | 0 | ▼tDissertations Abstracts International▼g85-12B.▲ | |
| 790 | ▼a0054▲ | ||
| 791 | ▼aPh.D.▲ | ||
| 792 | ▼a2024▲ | ||
| 793 | ▼aEnglish▲ | ||
| 856 | 4 | 0 | ▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17162007▼nKERIS▼z이 자료의 원문은 한국교육학술정보원에서 제공합니다.▲ |
Photoinduced Transfer of Spin-Polarized Charges at Semiconductor Interfaces[electronic resource]
자료유형
국외eBook
서명/책임사항
Photoinduced Transfer of Spin-Polarized Charges at Semiconductor Interfaces [electronic resource].
개인저자
발행사항
[S.l.] : Columbia University. 2024 Ann Arbor : ProQuest Dissertations & Theses , 2024
형태사항
1 online resource(111 p.)
일반주기
Source: Dissertations Abstracts International, Volume: 85-12, Section: B.
Advisor: Zhu, Xiaoyang.
Advisor: Zhu, Xiaoyang.
학위논문주기
Thesis (Ph.D.)--Columbia University, 2024.
요약주기
Charge transfer at the organic/inorganic semiconductor interfaces lies at the heart of interfacial photochemistry. While decades of research have shaped the current understanding that interfacial charge transfer depends crucially on energetic driving force and electronic coupling, much less is known about the role played by the spin degree of freedom. In particular, it is not clear how spin states evolve during the charge transfer process. With the advent of group 6 transition metal dichalcogenides (TMDC), a class of two-dimensional layered materials which permits the optical generation of spin-polarized electron-hole pairs in the monolayer limit, we now have the opportunity to investigate if charge transfer at an organic/inorganic interface could enable the transfer of spin polarization. Using time-resolved Faraday rotation and transient absorption spectroscopy, it is found in the MoSe2/H2Pc and C60/WS2 heterostructures that the photoinduced hole transfer from MoSe2 to H2Pc and electron transfer from WS2 to C60 results in spin polarization lifetimes one order of magnitude longer than that of a monolayer. In the WS2/MoSe2/H2Pc heterostructure, the addition of a WS2 monolayer drives the dissociation of electron-hole pairs bound at the MoSe2/H2Pc interface and leads to the observation of nanosecond-long spin polarization at room temperature. These findings evidence the photoinduced transfer of spin polarization, a mechanism which could potentially be exploited to enhance the efficiency and selectivity of photochemical reactions involving angular momentum change, and may be generalized to other organic/inorganic interfaces composed of crystalline semiconductors with spin-momentum locking.
주제
ISBN
9798383045138
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