Astrid M. Müller

Highly active mixed-metal nanosheet water oxidation catalysts made by pulsed-laser ablation in liquids.

Surfactant-free mixed-metal hydroxide water oxidation nanocatalysts were synthesized by pulsed-laser ablation in liquids. In a series of [Ni-Fe]-layered double hydroxides with intercalated nitrate and water, [Ni1-xFex(OH)2](NO3)y(OH)x-y·nH2O, higher activity was observed as the amount of Fe decreased to 22%. Addition of Ti(4+) and La(3+) ions further enhanced electrocatalysis, with a lowest overpotential of 260 mV at 10 mA cm(-2). Electrocatalytic water oxidation activity increased with the relative proportion of a 405.1 eV N 1s (XPS binding energy) species in the nanosheets.

Effect of interlayer anions on [NiFe]-LDH nanosheet water oxidation activity

We synthesized nickel–iron layered double hydroxide ([NiFe]-LDH) nanosheets with different interlayer anions to probe their role in water oxidation catalysis. In alkaline electrolyte in ambient air, carbonate rapidly replaced other interlayer anions and catalytic activity was highest. Electrocatalytic water oxidation in virtually carbonate-free alkaline electrolyte revealed that activity was a function of anion basicity. Our [NiFe]-LDH nanosheets, prepared by pulsed laser ablation in liquids, were regenerated in carbonate-containing aqueous KOH. Anion binding motifs were assessed by X-ray photoelectron spectroscopy in combination with density functional theory calculations, suggesting that nitrite species bound to edge-site Fe in the precatalyst correlated with higher water oxidation activity.

Photoluminescence-based measurements of the energy gap and diffusion length of Zn3P2

The steady-state photoluminescence spectra of zinc phosphide (Zn_3P_2) wafers have revealed a fundamental indirect band gap at 1.38 eV, in close proximity to the direct band gap at 1.50 eV. These values are consistent with the values for the indirect and direct band gaps obtained from analysis of the complex dielectric function deduced from spectroscopic ellipsometric measurements. Bulk minority carrier lifetimes of 20 ns were observed by time-resolved photoluminescence decay measurements, implying minority-carrier diffusion lengths of ≥ 7 µm.

Factors affecting bismuth vanadate photoelectrochemical performance

Bismuth vanadate is a promising photoanode material, but recent reports on undoped BiVO4 without sublayers and co-catalysts showed large variations in photocurrent generation. We addressed this issue by correlating photoelectrochemical performance with physical properties. We devised a novel anodic electrodeposition procedure with iodide added to the aqueous plating bath, which allowed us to prepare BiVO4 photoanodes with virtually identical thicknesses but different morphologies, and we could control surface Bi content. Morphologies were quantified from SEM images as distributions of crystallite areas and aspect-ratio-normalised diameters, and their statistical moments were derived. We could obtain clear photocurrent generation trends only from bivariate data analysis. Our experimental evidence suggests that a combination of low Bi/V ratio, small aspect-ratio-normalised diameters, and crystallites sizes that were small enough to provide efficient charge separation yet sufficiently large to prevent mass transport limitations led to highest photoelectrochemical performance.

Experimental and computational study of BODIPY dye-labeled cavitand dynamics

Understanding the distance distribution and dynamics between moieties attached to the walls of a resorcin[4]arene cavitand, which is switchable between an expanded kite and a contracted vase form, might enable the use of this molecular system for the study of fundamental distance-dependent interactions. Toward this goal, a combined experimental and molecular dynamics (MD) simulation study on donor/acceptor borondipyrromethene (BODIPY) dye-labeled cavitands present in the vase and kite forms was performed. Direct comparison between anisotropy decays calculated from MD simulations with experimental fluorescence anisotropy data showed excellent agreement, indicating that the simulations provide an accurate representation of the dynamics of the system. Distance distributions between the BODIPY dyes were established by comparing time-resolved Förster resonance energy transfer experiments and MD simulations. Fluorescence intensity decay curves emulated on the basis of the MD trajectories showed good agreement with the experimental data, suggesting that the simulations present an accurate picture of the distance distributions and dynamics in this molecular system and provide an important tool for understanding the behavior of extended molecular systems and designing future applications.

Passivation of Zn3P2 substrates by aqueous chemical etching and air oxidation

Surface recombination velocities measured by time-resolved photoluminescence and compositions of Zn_(3)P_2 surfaces measured by x-ray photoelectron spectroscopy (XPS) have been correlated for a series of wet chemical etches of Zn_(3)P_2 substrates. Zn_(3)P_2 substrates that were etched with Br_2 in methanol exhibited surface recombination velocity values of 2.8 × 10^4 cm s^(−1), whereas substrates that were further treated by aqueous HF–H_(2)O_2 exhibited surface recombination velocity values of 1.0 × 10^4 cm s^(−1). Zn_(3)P_2 substrates that were etched with Br_2 in methanol and exposed to air for 1 week exhibited surface recombination velocity values of 1.8 × 10^3 cm s^(−1), as well as improved ideality in metal/insulator/semiconductor devices.

Mixed-Metal Tungsten Oxide Photoanode Materials Made by Pulsed-Laser in Liquids Synthesis

Globally scalable sunlight-driven devices that convert solar energy into storable fuels will require efficient light absorbers that are made of non-precious elements. Suitable photoanode materials are yet to be discovered. Here we utilised the timesaving nature of pulsed-laser-in-liquids synthesis and prepared a series of neat and mixed-metal tungsten oxide photoanode materials to investigate the effect of ad-metals on optical and photocurrent generation properties. We obtained sub-μm-sized materials with different colours from W, Al, Ta, or first-row transition metal targets in water or aqueous ammonium metatungstate solutions. We observed metastable polymorphs of WO3 and tungsten oxides with varying degrees of oxygen deficiency. Pulsed-laser in liquids synthesis of Ni in ammonium metatungstate solutions produce hollow spheres (with ≤6 % Ni with respect to W). Photocurrent generation in strong aqueous acid is highest in mixed-metal tungsten oxide photoanode materials with around 5 % of iron or nickel.

Complex nanomineral formation utilizing kinetic control by PLAL

We used pulsed-laser ablation in liquids (PLAL) of Cu or Zn foil targets in water or in aqueous Cu or Zn salt solutions. PLAL in neat water generated mixtures of metal and (thermodynamically preferred) metal oxide nanomaterials, whereas the availability of select dissolved anions predictably led to the fabrication of more complex phase-pure nanominerals. PLAL of Cu foil in aqueous CuCl2 solution produced nano-paratacamite, Cu2Cl(OH)3, whereas nano-rouaite, Cu2(NO3)(OH)3, was formed in aqueous Cu(NO3)2 and NH4OH solution. Likewise, we synthesized simonkolleite, Zn5(OH)8Cl2·H2O, or layered zinc hydroxide nitrate, Zn5(OH)8(NO3)2·2H2O, nanoparticles by PLAL of Zn targets in aqueous ablation liquids with added ZnCl2 and NH4OH or Zn(NO3)2, respectively. Bimetallic zincian paratacamite resulted from PLAL of Cu foil in aqueous Cu and Zn chloride solution. Our results show that kinetic control exceeded thermodynamic product formation during nanosecond ultraviolet PLAL.

Driving Force Dependence of Electron Transfer from Electronically Excited [Ir(COD)(μ-Me_2pz)]_2 to Photo-Acid Generators

We report the rates of electron transfer (ET) reactions of electronically excited [Ir(COD)(μ-Me2pz)]2 with onium salt photoacid generators (PAGs). The reduction potentials of the PAGs span a large electrochemical window that allows determination of the driving force dependence of the ET reactions. Rate constants of ET from electronically excited [Ir(COD)(μ-Me2pz)]2 to onium PAGs are determined by the reaction driving force until the diffusion limit in acetonitrile is reached.