ABSTRACT
Quantum information processing requires quantum registers based on coherently interacting quantum bits. The dipolar couplings between nitrogen vacancy (NV) centres with nanometre separation makes them a potential platform for room-temperature quantum registers. The fabrication of quantum registers that consist of NV centre arrays has not advanced beyond NV pairs for several years. Further scaling up of coupled NV centres by using nitrogen implantation through nanoholes has been hampered because the shortening of the separation distance is limited by the nanohole size and ion straggling. Here, we demonstrate the implantation of C5N4Hn from an adenine ion source to achieve further scaling. Because the C5N4Hn ion may be regarded as an ideal point source, the separation distance is solely determined by straggling. We successfully demonstrate the fabrication of strongly coupled triple NV centres. Our method may be extended to fabricate small quantum registers that can perform quantum information processing at room temperature.
ABSTRACT
Nanostructures composed of conjugated polymers or π-conjugated molecules provide sensing platforms with large specific surface areas. One of the feasible approaches to accessing such nanostructured miniaturized sensors with ultrahigh sensitivity is to develop a network of organic nanowires with optical/electronic properties that can measure signals upon interacting with the analytes at their surfaces. In this work, organic nanowires with controlled number density and uniform length were fabricated by one-dimensional solid-state polymerization of 9,9'-spirobi[9 H-fluorene] (SBF) derivatives triggered by high-energy single particles. SBF was chosen as a conjugated molecular motif with the interplay of high density of π-electrons, high solubility, and uniform solid-state structures, allowing us to fabricate sensing platforms via solution processing. The as-deposited energy density in linear polymerization nanospace was theoretically analyzed by a collision model, interpreting nanowire sizes at subnanometer levels. The substitution of bromine atoms was confirmed to be effective not only for the higher collision probability of the incident particles but also for the remarkable increase in radiolytic neutral radical yield via C-Br cleavages or electron-dissociative attachments onto the bromine atoms. The fluorescence spectra of SBF-based nanowires were different from those of SBF derivatives due to extended bond formation as a result of polymerization reactions. Fluorescence was quenched by the addition of nitrobenzene, indicating the potential use of our nanowires for fluorometric sensing applications. Microwave-based conductivity measurements revealed that the SBF-based nanowires exhibited charge carrier transport property upon photoexcitation, and that the conductivity was changed upon treatment with nitrobenzene vapors. The presented strategy of bromination of aromatic rings for efficient fabrication of controlled nanowire networks with favorable fluorescent and charge transport properties of nanowires advances the development of nanostructured sensing systems.
ABSTRACT
The transmissions of carbon cluster ion beams through a tandem accelerator using several stripper gases (He, N2, CO2, and SF6) with a terminal voltage of 2.5 MV were measured as a function of the gas pressure in investigating the most suitable gas for cluster ion acceleration. This resulted in it being demonstrated that the highest transmission could be obtained using the smaller size gas, i.e., helium displayed the best performance of the four gases used. In addition, the ratio of transmissions of C(n) with helium and nitrogen increased with increases in the n, thus revealing that helium gas should prove the most effective in larger cluster ion acceleration using the same energy.
