We present a scalable wet chemical synthesis for a catalytically active nanostructured amorphous molybdenum sulfide material. The catalyst film is one of the most active nonprecious metal materials for electrochemical hydrogen evolution, drawing 10 mA/cm 2 at ∼200 mV overpotential. To identify the active phase of the material, we perform X-ray photoelectron spectroscopy after testing under a variety of conditions. As deposited, the catalyst resembles amorphous MoS 3 , but domains resembling MoS 2 in composition and chemical state are created under reaction conditions and may contribute to this material's high electrochemical activity. The activity scales with electrochemically active surface area, suggesting that the rough, nanostructured catalyst morphology also contributes substantially to the film's high activity. Electrochemical stability tests indicate that the catalyst remains highly active throughout prolonged operation. The overpotential required to attain a current density of 10 mA/ cm 2 increases by only 57 mV after 10 000 reductive potential cycles. Our enhanced understanding of this highly active amorphous molybdenum sulfide hydrogen evolution catalyst may facilitate the development of economical electrochemical hydrogen production systems.
Carrier recombination in single 10 nm wide m-plane homoepitaxial In0.15Ga0.85N/GaN quantum wells was examined by time-resolved photoluminescence. The radiative recombination time at 3.5 K was found to be short, about 0.5 ns. This value and the single-exponential luminescence decay show that the localized exciton recombination is not affected by the in-plane electric field. At room temperature, the nonradiative recombination was prevalent. The data indicate that the nonradiative recombination proceeds via efficient recombination centers. Complexes of Ga vacancies with oxygen and/or related interface defects are suggested to play this role and thus provide a direction for future improvements in materials' quality.
The invasive Argentine ant (Linepithema humile) is established worldwide and displaces native ant species. In northern California, however, the native winter ant (Prenolepis imparis) persists in invaded areas. We found that in aggressive interactions between the two species, P. imparis employs a potent defensive secretion. Field observations were conducted at P. imparis nest sites both in the presence and absence of L. humile. These observations suggested and laboratory assays confirmed that P. imparis workers are more likely to secrete when outnumbered by L. humile. Workers of P. imparis were also more likely to secrete near their nest entrances than when foraging on trees. One-on-one laboratory trials showed that the P. imparis secretion is highly lethal to L. humile, causing 79% mortality. The nonpolar fraction of the secretion was chemically analyzed with gas chromatography/mass spectrometry, and found to be composed of long-chain and cyclic hydrocarbons. Chemical analysis of dissected P. imparis workers showed that the nonpolar fraction is derived from the Dufour's gland. Based on these conclusions, we hypothesize that this chemical defense may help P. imparis to resist displacement by L. humile.
We demonstrate a vertical (<1°departure) and smooth (2.0 nm root mean square line-edge roughness (LER)) etch by chemically assisted Ar ion beam etching (CAIBE) in Cl 2 chemistry that is suitable for forming laser diode (LD) facets on nonpolar and semipolar oriented III-nitride devices. The etch profiles were achieved with photoresist masks and optimized CAIBE chamber conditions including the platen tilt angle and Cl 2 flow rate. Co-loaded studies showed similar etch rates of ∼60 nm min −1 for 2021 , 2021 , ( ¯¯) ( ¯) and m-plane orientations. The etched surfaces of LD facets on these orientations are chemically dissimilar (Ga-rich versus N-rich), but were visually indistinguishable, thus confirming the negligible orientation dependence of the etch. Continuous-wave blue LDs were fabricated on the semipolar 2021 ( ¯¯) plane to compare CAIBE and reactive ion etch (RIE) facet processes. The CAIBE process resulted in LDs with lower threshold current densities due to reduced parasitic mirror loss compared with the RIE process. The LER, degree of verticality, and model of the 1D vertical laser mode were used to calculate a maximum uncoated facet reflection of 17% (94% of the nominal) for the CAIBE facet. The results demonstrate the suitability of CAIBE for forming high quality facets for high performance nonpolar and semipolar III-N LDs.
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