Pathways Following Electron Injection: Medium Effects and Cross-Surface Electron Transfer in a Ruthenium-Based, Chromophore–Catalyst Assembly on TiO2
- Univ. of North Carolina, Chapel Hill, NC (United States). Dept. of Chemistry
- Univ. of North Carolina, Chapel Hill, NC (United States). Dept. of Chemistry; Univ. of Richmond, VA (United States). Dept. of Chemistry
- Univ. of North Carolina, Chapel Hill, NC (United States). Dept. of Chemistry; Chinese Academy of Sciences (CAS), Beijing (China). Inst. of Chemistry, Beijing National Lab. for Molecular Sciences, Lab. of Photochemistry
- Univ. of North Carolina, Chapel Hill, NC (United States). Dept. of Chemistry; Brookhaven National Lab. (BNL), Upton, NY (United States). Dept. of Chemistry
Interfacial dynamics following photoexcitation of the water oxidation assembly [((PO3H2)2bpy)2RuII(bpy-bimpy)RuII(tpy)(OH2)]4+, -[RuaII–RubII–OH2]4+, on nanocrystalline TiO2 electrodes, starting from either -[RuaII–RubII–OH2]4+ or -[RuaII–RubIII–OH2]5+, have been investigated. Transient absorption measurements for TiO2–[RuaII–RubII–OH2]4+ in 0.1 M HPF6 or neat trifluoroethanol reveal that electron injection occurs with high efficiency but that hole transfer to the catalyst, which occurs on the electrochemical time scale, is inhibited by local environmental effects. Back electron transfer occurs to the oxidized chromophore on the microsecond time scale. Photoexcitation of the once-oxidized assembly, TiO2–[RuaII–RubIII–OH2]5+, in a variety of media, generates -[RuaIII–RubIII–OH2]6+. The injected electron randomly migrates through the surface oxide structure reducing an unreacted -[RuaII–RubIII–OH2]5+ assembly to -[RuaII–RubII–OH2]4+. In a parallel reaction, -[RuaIII–RubIII–OH2]6+ formed by electron injection undergoes proton loss giving -[RuaII–RubIV$$=$$O]4+ with possible conversion to -[RuaII–RubII–OH2]4+ by an electrolyte-mediated reaction. In the following slow step, re-equilibration on the surface occurs either by reaction with added FeIII/II or by cross-surface electron transfer between spatially separated -[RuaII–RubIV$$=$$O]4+ and -[RuaII–RubII–OH2]4+ assemblies to give -[RuaII–RubIII–OH2]5+ with a half-time of t1/2 ~ 68 μs. Finally, these results and analyses show that the transient surface behavior of the assembly and cross-surface reactions play important roles in producing and storing redox equivalents on the surface that are used for water oxidation.
- Research Organization:
- Energy Frontier Research Centers (EFRC) (United States). Center for Solar Fuels (UNC EFRC)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- Grant/Contract Number:
- SC0001011
- OSTI ID:
- 1470650
- Journal Information:
- Journal of Physical Chemistry. C, Vol. 122, Issue 24; Related Information: UNC partners with University of North Carolina (lead); Duke University; University of Florida; Georgia Institute of Technology; University; North Carolina Central University; Research Triangle Institute; ISSN 1932-7447
- Publisher:
- American Chemical SocietyCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Web of Science
Core–shell structured titanium dioxide nanomaterials for solar energy utilization
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journal | January 2018 |
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catalysis (homogeneous)
catalysis (heterogeneous)
solar (photovoltaic)
solar (fuels)
photosynthesis (natural and artificial)
hydrogen and fuel cells
electrodes - solar
charge transport
materials and chemistry by design
synthesis (novel materials)
synthesis (self-assembly)