We show that a robust molybdenum hydride system can sustain photoelectrocatalysis of a hydrogen evolution reaction at boron‐doped, hydrogen‐terminated, p‐type silicon. The photovoltage for the system is about 600–650 mV and the current densities, which can be sustained at the photocathode in non‐catalytic and catalytic regimes, are similar to those at a photoinert vitreous carbon electrode. The kinetics of electrocatalysed hydrogen evolution at the photocathode are also very similar to those measured at vitreous carbon—evidently visible light does not significantly perturb the catalytic mechanism. Importantly, we show that the doped (1–10 Ω cm) p‐type Si can function perfectly well in the dark as an ohmic conductor and this has allowed direct comparison of the cyclic voltammetric behaviour of the response of the system under dark and illuminated conditions at the same electrode. The p‐type Si we have employed optimally harvests light energy in the 600–700 nm region and with 37 mW cm?2 illumination in this range; the light to electrochemical energy conversion is estimated to be 2.8 %. The current yield of hydrogen under broad tungsten halide lamp illumination at 90 mW cm?2 is (91±5) % with a corresponding chemical yield of (98±5) %. 相似文献
The title copper complex, [Cu(dl ‐DAP)2(H2O)2]·2H2O or [Cu(C3H7N2O2)2(H2O)2]·2H2O, prepared from the non‐protein amino acid dl ‐2,3‐diaminopropionic acid (dl ‐HDAP), has a center of symmetry and a distorted octahedral coordination, with four N atoms in equatorial positions and two water molecules in apical sites. The water molecule of crystallization is hydrogen bonded to the deprotonated carboxylate group of the ligand. 相似文献
Quantitative passive scalar measurements were performed in an incompressible planar mixing layer at Reδ up to 104 using planar laser-induced fluorescence of acetone seeded into one side of the layer. Probability density functions compiled
from sets of images showed a preferred mixture composition, favoring the high-speed fluid, which extended across the layer.
This preferred composition produced non-marching PDFs and an inflection in the average mixture fraction profile. The spatial
resolution of the experiment was found to be sufficient to accurately measure the fraction of mixed fluid within the layer.
The mixed fluid fraction was found to increase to an asymptotic value of 0.5 by Reδ ≈ 5,000, the approximate location of turbulent transition, in contrast to high Schmidt number experiments which show minimal
mixing before the transition point.
Received: 5 October 1999 / Accepted: 9 February 2001 相似文献
Given self-adjoint operators Hj, on Hilbert spaces ??j, j = 0,l, and J ∈ ?? (??0, ??1) (where ?? (??0 ??1) denotes the set of bounded linear operators from ??0to ??1), define the wave operators where P0 is the projection onto the subspace for absolute continuity for H0. We use (i) to study the scattering problem associated with a pair of equations each of the form where L is a positive, self-adjoint operator on a Hilbert space X, m is a positive integer and the αj are distinct positive constants. Methods patterned after those of Kato are used to study two equations (that is for L = L0 and L = Ll) each of the form (ii). We show that they are equivalent to equations of the form where each ?k is a self-adjoint operator on an associated Hilbert space ??k. Now suppose~he-wave operators W±,(L1L0) exist and are complete. Then we can find a J ∈ ??(H1H0) such that W+(?l, ?0,J) exists. In the case where Lo and L1 have the same domain, ??1 and ??0 are equal as vector spaces, and under certain conditions (on Li, i = 0, 1) ??0 and ??1 have equivalent norms. Assuming these conditions, let J'∈ ??(??1' ??0) be the identity map. We show that (with an additional assumption on L0 and L1) W+(?1?0,J) exists andisequal to W+(?l,?0, J). 相似文献
We have measured the3He concentration dependence of the thermal boundary resistanceRB between3He?4He dilute mixtures and submicron sintered silver between 10 and 150 mK. For concentrations greater than one percent, the results for the boundary resistance per inverse volume are insensitive to the concentration and have a magnitude similar to that predicted by the acoustic mismatch theory. For concentrations less than one percent, we observe an increase ofRB for decreasing concentrations. 相似文献