Publications by authors named "Ann L Greenaway"

Article Synopsis
  • - Conjugated polymers, like poly(NDI2OD-T2) (N2200), are popular in organic solar cells because they absorb near-infrared light well, but they have issues with short excited-state lifetimes and limited photocurrent contribution compared to their paired donors.
  • - This study investigates whether the N2200's performance characteristics are due to its polymer structure or external factors by comparing it to model compounds with similar donor-acceptor configurations in a solution.
  • - Findings reveal that the model compounds have even shorter excited-state lifetimes than N2200, suggesting that strong electronic interactions and coupling are responsible for the rapid decay to the ground state in both cases.
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Cation disorder is an established feature of heterovalent ternary nitrides, a promising class of semiconductor materials. A recently synthesized wurtzite-family ternary nitride, ZnTiN, shows potential for durable photoelectrochemical applications with a measured optical absorption onset of 2 eV, which is 1.4 eV lower than previously predicted, a large difference attributed to cation disorder.

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Delamination of the electron-transporting polymer N2200 from indium tin oxide (ITO) in aqueous electrolytes is mitigated by modifying ITO with an azide-functionalized phosphonic acid (PA) which, upon UV irradiation, reacts with the polymer. The optical, electrochemical, and spectroelectrochemical properties of N2200 thin films are retained in aqueous and non-aqueous media.

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Polymer semiconductors are fascinating materials that could enable delivery of chemical fuels from water and sunlight, offering several potential advantages over their inorganic counterparts. These include extensive synthetic tunability of optoelectronic and redox properties and unique opportunities to tailor catalytic sites via chemical control over the nanoenvironment. Added to this is proven functionality of polymer semiconductors in solar cells, low-cost processability, and potential for large-area scalability.

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Photoelectrochemical fuel generation is a promising route to sustainable liquid fuels produced from water and captured carbon dioxide with sunlight as the energy input. Development of these technologies requires photoelectrode materials that are both photocatalytically active and operationally stable in harsh oxidative and/or reductive electrochemical environments. Such photocatalysts can be discovered based on co-design principles, wherein design for stability is based on the propensity for the photocatalyst to self-passivate under operating conditions and design for photoactivity is based on the ability to integrate the photocatalyst with established semiconductor substrates.

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Photoinduced electron transfer into mesoporous oxide substrates is well-known to occur efficiently for both singlet and triplet excited states in conventional metal-to-ligand charge transfer (MLCT) dyes. However, in all-organic dyes that have the potential for producing two triplet states from one absorbed photon, called singlet fission dyes, the dynamics of electron injection from singlet triplet excited states has not been elucidated. Using applied bias transient absorption spectroscopy with an anthradithiophene-based chromophore () adsorbed to mesoporous indium tin oxide (), we modulate the driving force and observe changes in electron injection dynamics.

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Nitride materials feature strong chemical bonding character that leads to unique crystal structures, but many ternary nitride chemical spaces remain experimentally unexplored. The search for previously undiscovered ternary nitrides is also an opportunity to explore unique materials properties, such as transitions between cation-ordered and -disordered structures, as well as to identify candidate materials for optoelectronic applications. Here, we present a comprehensive experimental study of MgSnN, an emerging II-IV-N compound, for the first time mapping phase composition and crystal structure, and examining its optoelectronic properties computationally and experimentally.

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Thin films with tunable and homogeneous composition are required for many applications. We report the synthesis and characterization of a new class of compositionally homogeneous thin films that are amorphous solid solutions of AlO and transition metal oxides (TMO) including VO, CrO, MnO, FeO, CoO, NiO, CuO, and ZnO. The synthesis is enabled by the rapid decomposition of molecular transition-metal nitrates TM(NO) at low temperature along with precondensed oligomeric Al(OH)(NO) cluster species, both of which can be processed from aq solution.

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