We report heating rate measurements in a microfabricated gold-onsapphire surface electrode ion trap with trapping height of approximately 240 µm. Using the Doppler recooling method, we characterize the trap heating rates over an extended region of the trap. The noise spectral density of the trap falls in the range of noise spectra reported in ion traps at room temperature. We find that during the first months of operation the heating rates increase by approximately one order of magnitude. The increase in heating rates is largest in the ion loading region of the trap, providing a strong hint that surface contamination plays a major role for excessive heating rates. We discuss data found in the literature and possible relation of anomalous heating to sources of noise and dissipation in other systems, namely impurity atoms adsorbed on metal surfaces and amorphous dielectrics.
Spin-polarized two-dimensional electron states (2DESs) at surfaces and interfaces of
magnetically active materials attract immense interest because of the idea of
exploiting fermion spins rather than charge in next generation electronics. Applying
angle-resolved photoelectron spectroscopy, we show that the silicon surface of
GdRh2Si2 bears two distinct 2DESs, one being a Shockley
surface state, and the other a Dirac surface resonance. Both are subject to strong
exchange interaction with the ordered 4f-moments lying underneath the
Si-Rh-Si trilayer. The spin degeneracy of the Shockley state breaks down below
~90 K, and the splitting of the resulting subbands saturates
upon cooling at values as high as ~185 meV. The spin
splitting of the Dirac state becomes clearly visible around
~60 K, reaching a maximum of
~70 meV. An abrupt increase of surface magnetization at
around the same temperature suggests that the Dirac state contributes significantly
to the magnetic properties at the Si surface. We also show the possibility to tune
the properties of 2DESs by depositing alkali metal atoms. The unique
temperature-dependent ferromagnetic properties of the Si-terminated surface in
GdRh2Si2 could be exploited when combined with functional
adlayers deposited on top for which novel phenomena related to magnetism can be
anticipated.
The deposition of Cu seed layers for electrochemical Cu deposition (ECD) via atomic layer deposition (ALD) of copper oxide and subsequent thermal reduction at temperatures between 110 and 120°C was studied on different diffusion barrier systems. While optimization of the process is required on TaN with respect to reduction and plating, promising results were obtained on blanket PVD Ru. The plating results on layers of ALD Cu with underlying Ru even outperformed the ones achieved on PVD Cu seed layers with respect to morphology and resistivity. Applying the processes to via and line patterns gave similar results, suggesting that a combination of ALD Cu with PVD or ALD-grown Ru could significantly improve the ECD Cu growth.
We fabricate high-performance giant magnetoresistive (GMR) sensorics on Si wafers, which are subsequently thinned down to 100 mu m or 50 mu m to realize mechanically flexible sensing elements. The performance of the GMR sensors upon bending is determined by the thickness of the Si membrane. Thus, bending radii down to 15.5mm and 6.8mm are achieved for the devices on 100 mu m and 50 mu m Si supports, respectively. The GMR magnitude remains unchanged at the level of (15.3 +/- 0.4)% independent of the support thickness and bending radius. However, a progressive broadening of the GMR curve is observed associated with the magnetostriction of the containing Ni81Fe19 alloy, which is induced by the tensile bending strain generated on the surface of the Si membrane. An effective magnetostriction value of lambda(s) = 1.7 x 10(-6) is estimated for the GMR stack. Cyclic bending experiments showed excellent reproducibility of the GMR curves during 100 bending cycles
Atomistic mechanisms for the atomic layer deposition using the Cu(acac)2 (acac = acetylacetonate) precursor are studied using first-principles calculations and reactive molecular dynamics simulations. The results show that Cu(acac)2 chemisorbs on the hollow site of the Cu(110) surface and decomposes easily into a Cu atom and the acac-ligands. A sequential dissociation and reduction of the Cu precursor [Cu(acac)2 → Cu(acac) → Cu] are observed. Further decomposition of the acac-ligand is unfavorable on the Cu surface. Thus additional adsorption of the precursors may be blocked by adsorbed ligands. Molecular hydrogen is found to be nonreactive towards Cu(acac)2 on Cu(110), whereas individual H atoms easily lead to bond breaking in the Cu precursor upon impact, and thus release the surface ligands into the gas-phase. On the other hand, water reacts with Cu(acac)2 on a Cu2O substrate through a ligand-exchange reaction, which produces gaseous H(acac) and surface OH species. Combustion reactions with the main by-products CO2 and H2O are observed during the reaction between Cu(acac)2 and ozone on the CuO surface. The reactivity of different co-reactants toward Cu(acac)2 follows the order H > O3 > H2O.
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