In this work, we combine self-assembly and top-down methods to create hybrid junctions consisting of single organic molecular monolayers sandwiched between metal and/or single-crystalline semiconductor nanomembrane based electrodes. The fabrication process is fully integrative and produces a yield loss of less than 5% on-chip. The nanomembrane-based electrodes guarantee a soft yet robust contact to the molecules where the presence of pinholes and other defects becomes almost irrelevant. We also pioneer the fabrication and characterization of semiconductor/molecule/semiconductor tunneling heterojunctions which exhibit a double transition from direct tunneling to field emission and back to direct tunneling, a phenomenon which has not been reported previously.

As EUV approaches high volume manufacturing, reticle defectivity becomes an even more relevant topic for further investigation. Current baseline strategy for EUV defectivity management is to design, build and maintain a clean system without pellicle. In order to secure reticle front side particle adders to an acceptable level for high volume manufacturing, EUV pellicle is being actively investigated. Last year ASML reported on our initial EUV pellicle feasibility. In this paper, we will update on our progress since then. We will also provide an update to pellicle requirements published last year. Further, we present experimental results showing the viability and challenges of potential EUV pellicle materials, including, material properties, imaging capability, scalability and manufacturability.

The optical properties of aluminum hole arrays fabricated via colloidal lithography were investigated. By tuning the hole diameter and hole spacing independently, their influence on the Bloch wave−surface plasmon polariton (BW-SPP) and localized surface plasmon resonances resonances (LSPR) could be identified. The aluminum hole arrays were used to enhance the fluorescence of a dibenzoylmethanatoboron difluoride (DBMBF 2 ) dye. The dye exhibits the advantageous property of forming an exciplex with aromatic compounds. The interaction of DBMBF 2 monomer fluorescence and DBMBF 2 −toluene exciplexes with Al hole arrays is studied. Furthermore, the respective roles of the BW-SPPs and LSPRs were studied through tuning of the plasmon resonances from the UV excitation wavelength (λ ext = 385 nm) through the visible emission range (400−550 nm). Monomer emission was predominately enhanced by BW-SPPs while exciplex emission showed a contribution from both BW-SPPs and LSPRs. Fluorescence enhancement of 3.8 was observed for DBMBF 2 −toluene exciplex emission from 26 nm thick polymer films. Aluminum hole arrays are shown to be attractive structures for fluorescence enhancing applications with excitation in the UV and stable oxide coatings.

We describe and characterize an experimental apparatus that has been used to study interactions between ultracold lithium atoms and ytterbium ions. The preparation of ultracold clouds of Li atoms is described as well as their subsequent transport and overlap with Yb + ions trapped in a Paul trap. We show how the kinetic energy of the ion after interacting with the atoms can be obtained by laser spectroscopy. We analyze the dynamics of the buffer-gas-cooled ion after releasing the atoms, which indicates that background heating, due to electric-field noise, limits attainable buffer gas cooling temperatures. This effect can be mitigated by increasing the density of the Li gas in order to improve its cooling power. Imperfections in the Paul trap lead to so-called excess micromotion, which poses another limitation to the buffer gas cooling. We describe in detail how we measure and subsequently minimize excess micromotion in our setup. We measure the effect of excess micromotion on attainable ion temperatures after buffer gas cooling and compare this to molecular dynamics simulations, which describe the observed data very well.

We propose a new scalable architecture for trapped ion quantum computing that combines optical tweezers delivering qubit state-dependent local potentials with oscillating electric fields. Since the electric field allows for long-range qubit-qubit interactions mediated by the center-of-mass motion of the ion crystal alone, it is inherently scalable to large ion crystals. Furthermore, our proposed scheme does not rely on either ground-state cooling or the Lamb-Dicke approximation. We study the effects of imperfect cooling of the ion crystal, as well as the role of unwanted qubit-motion entanglement, and discuss the prospects of implementing the state-dependent tweezers in the laboratory.

The fluorescent spectra in combination with gas response behavior of acrylic polymers doped with dibenzoyl(methanato)boron difluoride (DBMBF2) were studied by fluorescence spectroscopy and time-resolved fluorescence lifetime. The role of acrylic matrix polarity upon the fluorescence spectra and fluorescence lifetime was analyzed. Changes in emission of the dye doped polymers under exposure to toluene, n-hexane and ethanol were monitored. The fluorescence lifetimes were measured for the singlet excited state as well as the exciplex formed between DBMBF2 and toluene. A reduction of the transition energy to the first singlet-excited state in the four polymers was observed, compared to solution. Reversible exciplex formation, viz. a red shifted fluorescence emission was perceived when exposing the polymers to toluene, while for hexane and ethanol only reversible reduction of the fluorescence occurred. Longer singlet and shorter exciplex lifetimes were observed for non-polar matrixes. The latter mechanism is explained in function of the lower charge transfer character of the exciplex in non-polar matrixes. Additionally, the quantum yield of the dye in the polymer matrix increased almost seventh-fold compared to values for solution.

We propose a method for generating programmable interactions in one-and two-dimensional trapped-ion quantum simulators. Here we consider the use of optical tweezers to engineer the sound-wave spectrum of trapped ion crystals. We show that this approach allows us to tune the interactions and connectivity of the ion qubits beyond the power-law interactions accessible in current setups. We demonstrate the experimental feasibility of our proposal using realistic tweezer settings and experimentally relevant trap parameters to generate the optimal tweezer patterns to create target spin-spin interaction patterns in both one-and two-dimensional crystals. Our approach will advance quantum simulation in trapped-ion platforms as it allows them to realize a broader family of quantum spin Hamiltonians.

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