Spin-crossover complexes in nanoscale devices: main ingredients of the molecule–substrate interactions

Spin-crossover complexes embedded in nanodevices experience effects that are absent in the bulk that can modulate, quench and even suppress the spin-transition. In this work we explore, by means of state-of-the-art quantum chemistry calculations, different aspects of the integration of SCO molecules on active nanodevices, such as the geometry and energetics of the interaction with the substrate, extension of the charge transfer between the substrate and SCO molecule, impact of the applied external electric field on the spin-transition, and sensitivity of the transport properties on the local conditions of the substrate. We focus on the recently reported encapsulation of Fe(II) spin-crossover complexes in single-walled carbon nanotubes, with new measurements that support the theoretical findings. Even so our results could be useful to many other systems where SCO phenomena take place at the nanoscale, the spin-state switching is probed by an external electric field or current, or the substrate is responsible for the quenching of the SCO mechanism.Ministerio de Ciencia e Innovación de España, Agencia Estatal de Investigación de España y Fondos FEDER. (MCI/ AEI/FEDER,UE) PGC2018-101689-B-I00, RTI2018-096075-A-C22 y RYC2019-028429-

Spin-state-dependent electrical conductivity in single-walled carbon nanotubes encapsulating spin-crossover molecules

Spin crossover (SCO) molecules are promising nanoscale magnetic switches due to their ability to modify their spin state under several stimuli. However, SCO systems face several bottlenecks when downscaling into nanoscale spintronic devices: their instability at the nanoscale, their insulating character and the lack of control when positioning nanocrystals in nanodevices. Here we show the encapsulation of robust Fe-based SCO molecules within the 1D cavities of single-walled carbon nanotubes (SWCNT). We find that the SCO mechanism endures encapsulation and positioning of individual heterostructures in nanoscale transistors. The SCO switch in the guest molecules triggers a large conductance bistability through the host SWCNT. Moreover, the SCO transition shifts to higher temperatures and displays hysteresis cycles, and thus memory effect, not present in crystalline samples. Our results demonstrate how encapsulation in SWCNTs provides the backbone for the readout and positioning of SCO molecules into nanodevices, and can also help to tune their magnetic properties at the nanoscale.Marie Skłodowska-Curie Actions 74657Programa de Atracción del Talento Investigador 2017-T1/IND-5562Ministerio de Economia, Industria y Competitividad CTQ2017-86060-P, PID2019-111479GB-100, MAT 2017-8225, GC2018-101689-B-I00Consejo Europeo de Investigación ERC-StG-307609, ERC-PoC-842606Comunidad Autónoma de Madrid MAD2D-CM S2013/ MIT-3007, PEJD-2017-PRE/IND-4037, Y2018/NMT- 4783NANOMAGCOST P2018/ NMT-432

Magnetic mechanically-interlocked porphyrin-carbon nanotubes

Resumen del póster presentado a la XXXVIII Reunión Bienal de la Real Sociedad Española de Química, celebrada en el Palacio de Congresos de Granada, del 27 de junio al 30 de junio de 2022.Magnetic molecules have been proposed as versatile building blocks for quantum computing and molecular spintronics devices. The molecular spin can be used to encode quantum information in qubits or even perform logic operations as quantum gates with unmatched reproducibility and scalability. In spintronics, that same molecular spin can be used to generate spin currents in molecular based spin filters, spin switches or spin valves in carbon-nanotube/molecule hybrids, among other applications. Several strategies have been followed to couple the magnetic molecules to carbon nanotubes: direct physisorption of the molecules, covalent bonding or encapsulation of the magnetic molecules. We have developed the synthesis of mechanically interlocked rotaxane-like SWCNT derivatives (MINTs), in which the ring-closing metathesis of a U-shape molecule around SWCNTs is templated. In particular, we fabricated Cu2+ and Co2+ metalloporphyrin dimer rings mechanically interlocked around carbon nanotubes to form magnetic MINTs (mMINT). Magnetic porphyrins are selected due to their recently proved suitability as qubits, even preserving their magnetic properties and quantum coherence on surfaces. The mechanical bond places the porphyrin magnetic cores in close contact with the SWCNT without disturbing the molecular spin nor the carbon nanotube structure. The magnetic properties of the metallic dimers are preserved upon formation the mechanically interlocked hybrid.Peer reviewe

Fabrication of devices featuring covalently linked MoS2–graphene heterostructures

The most widespread method for the synthesis of 2D–2D heterostructures is the direct growth of one material on top of the other. Alternatively, flakes of different materials can be manually stacked on top of each other. Both methods typically involve stacking 2D layers through van der Waals forces—such that these materials are often referred to as van der Waals heterostructures—and are stacked one crystal or one device at a time. Here we describe the covalent grafting of 2H-MoS2 flakes onto graphene monolayers embedded in field-effect transistors. A bifunctional molecule featuring a maleimide and a diazonium functional group was used, known to connect to sulfide- and carbon-based materials, respectively. MoS2 flakes were exfoliated, functionalized by reaction with the maleimide moieties and then anchored to graphene by the diazonium groups. This approach enabled the simultaneous functionalization of several devices. The electronic properties of the resulting heterostructure are shown to be dominated by the MoS2–graphene interface.The authors acknowledge European Research Council (ERC-PoC- 842606 (E.M.P.); ERC-AdG-742684 (J. S.) and the MSCA program MSCA-IF-2019-892667 (N.M.S.), MINECO (CTQ2017-86060-P (E.M.P.) and CTQ2016-79419-R), Ministerio de Ciencia e Innovación (RTI2018-096075-A-C22 (E.B.), RYC2019-028429-I (E.B.)) the Comunidad de Madrid (MAD2D-CM S2013/ MIT-3007 (E.M.P.), Y2018/NMT-4783 (A.D.)) and the Programa de Atracción del Talento Investigador 2017-T1/IND-5562 (E.B.)). CzechNanoLab Research Infrastructure supported by MEYS CR (LM2018110) are gratefully acknowledged. IMDEA Nanociencia acknowledges support from the Severo Ochoa Programme for Centres of Excellence in R&D (MINECO, grant no. SEV-2016-0686).Peer reviewe

Transporte electrónico en heteroestructuras de dimensionalidad variada basadas en moléculas

Tesis Doctoral inédita leída en la Universidad Autónoma de Madrid, Facultad de Ciencias, Departamento de Física Teórica de la Materia Condensada. Fecha de Lectura: 13-06-202

Electron transport in mixed-dimensional heterostructures based on molecules

Tesis doctoral inédita leída en la Universidad Autónoma de Madrid. Fecha de lectura: 13-6-2022

Tunable Proton Conductivity and Color in a Nonporous Coordination Polymer via Lattice Accommodation to Small Molecules

International audienc

A Chemical Approach to 2D-2D Heterostructures Beyond Van Der Waals: High-Throughput On-Device Covalent Connection of MoS2 and Graphene

The most widespread method for the synthesis of 2D-2D heterostructures is the direct growth of one material on top of the other. Alternatively, one can manually stack flakes of different materials. Both methods are limited to one crystal/device at a time and involve interfacing the 2D materials through van der Waals forces, to the point that all these materials are known as van der Waals heterostructures. Synthetic chemistry is the paradigm of atomic-scale control, yet its toolbox remains unexplored for the construction of 2D-2D heterostructures. Here, we describe how to covalently connect 2H-MoS2 flakes to several single-layer graphene field-effect transistors simultaneously, and show that the final electronic properties of the MoS2-graphene heterostructure are dominated by the molecular interface. We use a bifunctional molecule with two chemically orthogonal anchor points, selective for sulphides and carbon-based materials. Our experiments highlight the potential of the chemical approach to build 2D-2D heterostructures beyond van der Waals. </p