RESUMO
The quest for developing quantum technologies is driven by the promise of exponentially faster computations, ultrahigh performance sensing, and achieving thorough understanding of many-particle quantum systems. Molecular spins are excellent qubit candidates because they feature long coherence times, are widely tunable through chemical synthesis, and can be interfaced with other quantum platforms such as superconducting qubits. A present challenge for molecular spin qubits is their integration in quantum devices, which requires arranging them in thin films or monolayers on surfaces. However, clear proof of the survival of quantum properties of molecular qubits on surfaces has not been reported so far. Furthermore, little is known about the change in spin dynamics of molecular qubits going from the bulk to monolayers. Here, a versatile bottom-up method is reported to arrange molecular qubits as functional groups of self-assembled monolayers (SAMs) on surfaces, combining molecular self-organization and click chemistry. Coherence times of up to 13 µs demonstrate that qubit properties are maintained or even enhanced in the monolayer.
RESUMO
In this manuscript we present a versatile platform for introducing functional redox species into tailor-made 3D redox polymer networks. Electrochemical characterization based on cyclic voltammetry is applied to verify the immobilization of the redox species within the conducting networks. Ultimately this strategy shall be extended to (photo)electrocatalytic applications which will profit from the conducting polymer matrix. Soluble precursor copolymers are synthesized via radical copolymerization of vinyltriphenylamine (VTPA) with chloromethylstyrene (CMS) in different ratios, whereas CMS is subsequently converted into azidomethylstyrene (AMS) to yield poly(VTPA-co-AMS) copolymers. Spin-coating of poly(VTPA-co-AMS) on gold electrodes yields thin films which are converted into stable polymer network structures by electrochemical crosslinking of the polymer chains via their pendant triphenylamine groups to yield N,N,N',N'-tetraphenylbenzidine (TPB) crosslinking points. Finally, the resulting redox-active, TPB-crosslinked films are functionalized with ethynylferrocene (EFc) as a representative redox probe using a click reaction. Main experimental tools are polarization modulation infrared reflection absorption spectroscopy and scan rate dependent cyclic voltammetry. Especially the latter proves the successful conversion and the immobilization of redox probes in the polymer matrix. The results are compared with the reference system of azide-terminated self-assembled monolayers on gold substrates, allowing to distinguish between free and immobilized EFc species.
RESUMO
Block copolymers have a wide range of functions in advanced electrochemistry because of their ability to self-assemble into ordered nanometer-sized structures, resulting in their extensive usage as nanoporous templates that can be electrochemically manipulated. These highly ordered nanoporous templates are used as working electrodes for electrodeposition and electropolymerization to build nanoelectrode arrays and can serve as models to study the diffusion pathway of redox-active units with regard to chemical modification of pores. The block copolymer system allows different morphologies to be utilized, but the most exploited structures are standing cylinders of the minority block that are etched to expose highly aligned porous nanoelectrode array templates. This review starts with introducing alumina and track-etched membranes as pioneer porous templates transitioning to the production of block copolymer films as succeeding templates, with a particular focus on both poly(styrene)-block-poly(methylmethacrylate) (PS-b-PMMA) and poly(styrene)-block-poly(lactide) (PS-b-PLA). The aim is to give fundamental insights of electrochemistry where functionality extends beyond to applications in the nanoscience field of biosensors and plastic electronics.