Growth Mechanism and Electronic Structure of Zn_3P_2 on the Ga-Rich GaAs(001) Surface

The growth of epitaxial Zn_3P_2 films on III–V substrates unlocks a promising pathway toward high-efficiency, earth-abundant photovoltaic devices fabricated on reusable, single-crystal templates. The detailed chemical, structural, and electronic properties of the surface and interface of pseudomorphic Zn_3P_2 epilayers grown on GaAs(001) were investigated using scanning tunneling microscopy/spectroscopy and high-resolution X-ray photoelectron spectroscopy. Two interesting features of the growth process were observed: (1) vapor-phase P4 first reacts with the Ga-rich GaAs surface to form an interfacial GaP layer with a thickness of several monolayers, and (2) a P-rich amorphous overlayer is present during the entire film growth process, beneath which a highly ordered Zn_3P_2 crystalline phase is precipitated. These features were corroborated by transmission electron micrographs of the Zn_3P_2/GaAs interface as well as density functional theory calculations of P reactions with the GaAs surface. Finally, the valence-band offset between the crystalline Zn_3P_2 epilayer and the GaAs substrate was determined to be ΔE_V = 1.0 ± 0.1 eV, indicating the formation of a hole-depletion layer at the substrate surface which may inhibit formation of an ohmic contact

MOF-Derived RuCo Catalyzes the Formation of a Plasticizer Alcohol from Renewable Precursors

The Guerbet reaction can be used for the condensation of simple bioalcohols, which simultaneously doubles the carbon count and increases the C:O ratio, to yield valuable commodity chemicals. Here, we report a metal–organic framework (MOF)-derived RuCo catalyst that furnishes 2-ethylhexanol, a plasticizer alcohol currently produced on a 2 Mt/a scale. While the industrial route requires propene, the MOF-derived catalyst uses 1-butanol and delivers turnover numbers up to 1.7 × 106 Ru–1. In combination with K3PO4, it serves as a fully heterogeneous catalyst system that yields the Guerbet alcohol without producing sodium butanoate, a common secondary product from the undesired Cannizzaro reaction

Metal–Organic Framework-Derived Guerbet Catalyst Effectively Differentiates between Ethanol and Butanol

RuNi nanoparticles supported on a metal–organic framework (RuNi@MOF) and formed in situ from a ruthenium complex enclosed inside a nickel-based MOF act as a highly active catalyst for the Guerbet reaction of ethanol to 1-butanol, providing turnover numbers up to 725 000 Ru–1. Negligible activity of the RuNi@MOF ethanol upgrading catalyst system toward chemically similar 1-butanol makes it possible to synthesize the competent Guerbet substrate 1-butanol with >99% selectivity

Use of a ruthenium-containing conjugated polymer as a photosensitizer in photovoltaic devices fabricated by a layer-by-layer deposition process

Multilayer polymer films composed of a ruthenium terpyridine complex containing poly(p-phenylenevinylene) (Ru-PPV) and sulfonated polyaniline (SPAN) were prepared by a layer-by-layer electrostatic self-assembly deposition. The deposition process was carried out from SPAN solution in water and Ru-PPV in dimethylformamide (DMF). Optical-quality multilayer thin films were obtained. The film growth process was monitored by quartz crystal microbalance, and the surface morphology of the films was studied by atomic force microscopy. It was found that the properties of the multilayer films were dependent on deposition conditions such as the pH of the SPAN solution, the presence of salt in the polymer solutions, and the post-film-forming thermal annealing process. Cross-section transmission electron microscopic images suggested that there was no stratified structure formed in the multilayer films. Photovoltaic cells were fabricated by sandwiching the multilayer films between indium-tin-oxide and aluminum electrodes. The device performances were examined by illumination with AM 1.5 simulated solar light. The power conversion efficiencies of these devices were on the order of 10~3%. The maximum incident photon-to-electron conversion efficiency (IPCE) of the devices was found to be approximately 2% at 510 nm, which is consistent with the absorption maximum of the ruthenium complex. This indicates that the photosensitization process is due to the electronic excitation of the ruthenium complex. © 2006 American Chemical Society.link_to_subscribed_fulltex