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020 ▼a 9780438349803
035 ▼a (MiAaPQ)AAI10843258
035 ▼a (MiAaPQ)unc:18103
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0491 ▼f DP
0820 ▼a 540
1001 ▼a Motley, Tyler Chase.
24510 ▼a Control of Lateral Electron Transfer Between Compounds Anchored to Semiconductor Interfaces.
260 ▼a [S.l.] : ▼b The University of North Carolina at Chapel Hill., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 240 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B.
500 ▼a Adviser: Gerald J. Meyer.
5021 ▼a Thesis (Ph.D.)--The University of North Carolina at Chapel Hill, 2018.
520 ▼a The need for a clean and renewable energy source is paramount to long term global economic and energy security and is the motivation for this work. The sun is one of the largest sources of renewable energy available. Dye-sensitized solar and pho
520 ▼a Chapters 2-4 explore the effect of molecular structure on lateral electron transfer kinetics. In Chapters 2 and 3, the effect of 4 and 4' substituents are examined using a series of compounds of the type [Ru(R2bpy) 2(bpy')]2+, where R2bpy was a
520 ▼a Other processes relevant to dye-sensitized technologies are also explored. Thermal, bimolecular electron transfer between CoII and RuIII polypyridyl compounds that follows Marcus-inverted behavior is observed in acetonitrile and is the focus of
590 ▼a School code: 0153.
650 4 ▼a Chemistry.
690 ▼a 0485
71020 ▼a The University of North Carolina at Chapel Hill. ▼b Chemistry.
7730 ▼t Dissertation Abstracts International ▼g 80-01B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0153
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999915 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자 ▼b 관리자