Fabrication Of Molecular Devices Research Articles

Advancing Artificial Cells with Functional Compartmentalized Polymeric Systems - In Honor of Wolfgang Meier.

The fundamental building block of living organisms is the cell, which is the universal biological base of all living entities. This micrometric mass of cytoplasm and the membrane border have fascinated scientists due to the highly complex and multicompartmentalized structure. This specific organization enables numerous metabolic reactions to occur simultaneously and in segregated spaces, without disturbing each other, but with a promotion of inter- and intracellular communication of biomolecules. At present, artificial nano- and microcompartments, whether as single components or self-organized in multicompartment architectures, hold significant value in the study of life development and advanced functional materials and in the fabrication of molecular devices for medical applications. These artificial compartments also possess the properties to encapsulate, protect, and control the release of bio(macro)molecules through selective transport processes, and they are capable of embedding or being connected with other types of compartments. The self-assembly mechanism of specific synthetic compartments and thus the fabrication of a simulated organelle membrane are some of the major aspects to gain insight. Considerable efforts have now been devoted to design various nano- and microcompartments and understand their functionality for precise control over properties. Of particular interest is the use of polymeric vesicles for communication in synthetic cells and colloidal systems to reinitiate chemical and biological communication and thus close the gap toward biological functions. Multicompartment systems can now be effectively created with a high level of hierarchical control. In this way, these structures can not only be explored to deepen our understanding of the functional organization of living cells, but also pave the way for many more exciting developments in the biomedical field.

Host-guest assembly functionalization through molecular selective adsorption into chiral Kagome-like frameworks

Supramolecular self-assembly offers a feasible route for nanopatterning and functionality. The construction and precise control of selective adsorption at the molecular scale play essential roles in fundamental sciences and practical applications. Molecular tiling such as trihexagonal tiling Kagome networks has potential promising chemical and physical properties. Distorted Kagome-like networks controllable fabrication is possible by coupling molecular functional groups and substrate atoms. A chiral Kagome-like network was constructed using IFDO ([1,2-b]fluorene-6,12-dione) as precursor molecules complemented with molecular beam epitaxy and annealing strategies. Revealing arrangements of the assembled network of O-Cu metal coordination linked Kagome-like networks on the Cu(111) surface and their assembly mechanisms and cavity characteristics were explored in detail through scanning tunneling microscopy combined with density functional theory. Based on the electronic state difference between the hole center of the network and the molecular backbone, the host–guest network was successfully prepared by co-depositing C60 molecules. Kagome-like networks could as an efficient template for regulating the adsorption configuration of C60. Our results demonstrate a controllable and efficient method to design atomically precise ordered host–guest assemblies on solid surfaces, advancing the approach is yet another step toward the fabrication of molecular devices.

Structure Fabrication on Silicon at Atomic and Close-To-Atomic Scale Using Atomic Force Microscopy: Implications for Nanopatterning and Nanodevice Fabrication.

In this paper, the atomic-scale structure fabrication on Si (100) substrate using atomic force microscopy (AFM) with the aid of electrochemical and mechanical processes in a humid environment and under ambient conditions is studied. The local oxidation patterns are formed using platinum-coated tips with the aid of bias applied to the tip-substrate junction, and direct removal has been achieved using single crystal diamond tips, enabling the structure fabrication at the atomic and close-to-atomic scale. The depth and height of the etched trenches reached about 1 nm, which provides an approach for the fabrication of atomic-scale electrodes for molecular device development. Furthermore, material removal close to about three silicon atoms (~3.2 Å) has been achieved. This is important in molecular device fabrication. A detailed comparison among the nanopatterns and the material removal over bare and hydrofluoric acid (HF) treated silicon substrates is provided. This comparison is useful for the application of fabricating atomic-scale electrodes needed for the molecular electronic components. A deep understanding of atomic-scale material removal can be pushed to fabricate a single atomic protrusion by removing the neighbouring atoms so that the molecule can be attached to a single atom, thereby the AFM tip and Si substrate could act as the electrodes and the molecule between them as the channel, providing basic transistor actions in a molecular transistor design. In this paper, platinum-coated and single-crystal diamond tips are used to explain the oxide formations and direct material removal, respectively.

Synthesis and Surface Behaviour of NDI Chromophores Mounted on a Tripodal Scaffold: Towards Self-Decoupled Chromophores for Single-Molecule Electroluminescence.

This paper reports the efficient synthesis, absorption and emission spectra, and the electrochemical properties of a series of 2,6‐disubstituted naphthalene‐1,4,5,8‐tetracarboxdiimide (NDI) tripodal molecules with thioacetate anchors for their surface investigations. Our studies showed that, in particular, the pyrrolidinyl group with its strong electron‐donating properties enhanced the fluorescence of such core‐substituted NDI chromophores and caused a significant bathochromic shift in the absorption spectrum with a correspondingly narrowed bandgap of 1.94 eV. Cyclic voltammetry showed the redox properties of NDIs to be influenced by core substituents. The strong electron‐donating character of pyrrolidine substituents results in rather high HOMO and LUMO levels of ‐5.31 and ‐3.37 eV when compared with the parental unsubstituted NDI. UHV‐STM measurements of a sub‐monolayer of the rigid tripodal NDI chromophores spray deposited on Au(111) show that these molecules mainly tend to adsorb flat in a pairwise fashion on the surface and form unordered films. However, the STML experiments also revealed a few molecular clusters, which might consist of upright oriented molecules protruding from the molecular island and show electroluminescence photon spectra with high electroluminescence yields of up to 6×10−3. These results demonstrate the promising potential of the NDI tripodal chromophores for the fabrication of molecular devices profiting from optical features of the molecular layer.

Molecular Packing in a Triphenylene‐Surfactant Complex Monolayer: Unambiguous Determination of Electrostatically Driven Molecular Packing in a Triphenylene–Surfactant Complex Monolayer (Adv. Mater. Interfaces 13/2021)

Self-assembly is a technique of choice for the bottom-up fabrication of molecular devices. In article number 2100187, Snehasis Daschakraborty, Alpana Nayak, and co-workers report intricate details of the self-assembly processes and resultant ordered structures of a technologically useful molecular system comprising of discotic liquid crystal and double chain surfactant.

An estimation on the mechanical stabilities of SAMs by low energy Ar+ cluster ion collision

The stability of the molecular self-assembled monolayers (SAMs) is of vital importance to the performance of the molecular electronics and their integration to the future electronics devices. Here we study the effect of electron irradiation-induced cross-linking on the stability of self-assembled monolayer of aromatic 5,5′-bis(mercaptomethyl)-2,2′-bipyridine [BPD; HS-CH2-(C5H3N)2-CH2-SH] on Au (111) single crystal surface. As a refence, we also study the properties of SAMs of electron saturated 1-dodecanethiol [C12; CH3-(CH2)11-SH] molecules. The stability of the considered SAMs before and after electron-irradiation is studied using low energy Ar+ cluster depth profiling monitored by recording the X-ray photoelectron spectroscopy (XPS) core level spectra and the UV-photoelectron spectroscopy (UPS) in the valance band range. The results indicate a stronger mechanical stability of BPD SAMs than the C12 SAMs. The stability of BPD SAMs enhances further after electron irradiation due to intermolecular cross-linking, whereas the electron irradiation results in deterioration of C12 molecules due to the saturated nature of the molecules. The depth profiling time of the cross-linked BPD SAM is more than 4 and 8 times longer than the profiling time obtained for pristine and BPD and C12 SAMs, respectively. The UPS results are supported by density functional theory calculations, which show qualitative agreement with the experiment and enable us to interpret the features in the XPS spectra during the etching process for structural characterization. The obtained results offer helpful options to estimate the structural stability of SAMs which is a key factor for the fabrication of molecular devices.

Guiding Students to Understand the Nanoscale Charge Transport by the Mechanically Controllable Break Junction Technique

Fabrication of molecular devices will meet the demands of the miniaturization of traditional electronic devices. Although microfabrication based on the complementary metal-oxide–semiconductor process can fabricate high-quality single-molecule devices, the cost is high, leading to a challenge to provide a hands-on experiment in the teaching practice of charge transport through single-molecule devices. Here, we demonstrate the low cost and simple procedures associated with a mechanically controllable break junction (MCBJ) technique to fabricate single-molecule devices. On the basis of the MCBJ technique, the conductance of gold–gold atomic contacts and single-molecule junctions can be readily characterized. The teaching practice helps students understand charge transport at the single-molecule level, that is, the quantum tunneling mechanisms. Moreover, the MCBJ technique study provides students the opportunity to develop interdisciplinary thinking, which is vital for understanding, designing, and developing single-molecule electronics.

Selective Fabrication of Single-Molecule Junctions by Interface Engineering.

Recent progress in addressing electrically driven single-molecule behaviors has opened up a path toward the controllable fabrication of molecular devices. Herein, the selective fabrication of single-molecule junctions is achieved by employing the external electric field. For molecular junctions with methylthio (-SMe), thioacetate (-SAc), amine (-NH2 ), and pyridyl (-PY), the evolution of their formation probabilities along with the electric field is extracted from the plateau analysis of individual single-molecule break junction traces. With the increase of the electric field, the SMe-anchored molecules show a different trend in the formation probability compared to the other molecular junctions, which is consistent with the density functional theory calculations. Furthermore, switching from an SMe-anchored junction to an SAc-anchored junction is realized by altering the electric field in a mixed solution. The results in this work provide a new approach to the controllable fabrication and modulation of single-molecule junctions and other bottom-up nanodevices at molecular scales.

Drying Mediated Aggregation Pattern of CdTe QDs towards the Fabrication of Molecular Devices

Drying mediated self-aggregation patterns of CdTe colloidal QDs through simple evaporation method was reported. Thioglycolic acid (TGA) capped CdTe QDs were prepared in aqueous phase through colloidal route and their structural, optical and morphological behaviors were studied. The drying patterns of CdTe QDs were fabricated under a constant evaporation rate. The coffee ring effect and the drying pattern formations were studied for the TGA capped CdTe colloidal QDs suspension in an aqueous medium. The structural behavior of the CdTe QDs and the drying patterns were revealed by the X-ray diffraction analysis. The size-tunable optical properties of the prepared CdTe QDs were studied by the optical absorption and emission spectroscopy. The capping effects of TGA on CdTe QDs were confirmed by the FT-IR analysis. The surface morphology of the TGA capped CdTe QDs and the drying mediated aggregation patterns of CdTe colloidal suspension were studied by the scanning electron microscopy analysis. The drying mediated patterns from the evaporation technique were suggested as a simple technique for the fabrication of molecular devices.

Electric-Field-Induced Connectivity Switching in Single-Molecule Junctions.

SummaryThe manipulation of molecule-electrode interaction is essential for the fabrication of molecular devices and determines the connectivity from electrodes to molecular components. Although the connectivity of molecular devices could be controlled by molecular design to place anchor groups in different positions of molecule backbones, the reversible switching of such connectivities remains challenging. Here, we develop an electric-field-induced strategy to switch the connectivity of single-molecule junctions reversibly, leading to the manipulation of different connectivities in the same molecular backbone. Our results offer a new concept of single-molecule manipulation and provide a feasible strategy to regulate molecule-electrode interaction.

Single-Molecule Electrical Detection: A Promising Route toward the Fundamental Limits of Chemistry and Life Science.

The ultimate limit of analytical chemistry is single-molecule detection, which allows one to visualize the dynamic processes of chemical/biological interactions with single-molecule or single-event sensitivity and hence enables the study of stochastic fluctuations under equilibrium conditions and the observation of time trajectories and reaction pathways of individual species in nonequilibrated systems. In addition, such studies may also allow the direct observation of novel microscopic quantum effects and fundamental discoveries of underlying molecular mechanisms in organic reactions and biological processes that are not accessible in ensemble experiments, thus providing unique opportunities to solve the key problems of physical, chemical, and life sciences. Consequently, the field of single-molecule detection has received considerable attention and has witnessed tremendous advances in different directions in combination with other disciplines. This Account describes our ongoing work on the development of groundbreaking methods (termed "single-molecule electrical approaches") of translating the detailed processes of chemical reactions or biological functions into detectable electrical signals at the single-event level on the platform of single-molecule electronic devices, with a particular focus on graphene-molecule-graphene single-molecule junctions (GMG-SMJs) and silicon-nanowire-based single-molecule electrical nanocircuits. These nanocircuit-based architectures are complementary to conventional optical or mechanical techniques but exhibit obvious advantages such as the absence of problems associated with bleaching and fluorescent labeling. Dash-line lithography (DLL) is an efficient lithographic method of cutting graphene and forming carboxylic-acid-functionalized nanogapped graphene point contact arrays developed to address the formidable challenges of molecular device fabrication difficulty and poor stability. Molecules of interest terminated by amines on both ends can be covalently sandwiched between graphene point contacts to create high-throughput robust GMG-SMJs containing only one molecule as the conductive element. In conjunction with the ease of device fabrication and device stability, this feature distinguishes GMG-SMJs as a new testbed platform for single-molecule analysis characterized by high temporal resolution and superior signal-to-noise ratios. By exploiting the DLL method, we have fabricated molecular devices that are sensitive to external stimuli and are capable of transducing chemical/biochemical events into electrical signals at the single-molecule level, with notable examples including host-guest interaction, hydrogen bond dynamics, DNA intercalation, photoinduced conformational transition, carbocation formation, nucleophilic addition, and stereoelectronic effect. In addition to GMG-SMJs and considering compatibility with the silicon-based industry, we have also developed a reliable method of point-functionalizing silicon-nanowire-based nanotransistors to afford single-molecule electrical nanocircuits. This approach proved to be a robust platform for single-molecule electrical analysis capable of probing fast dynamic processes such as single-protein detection, DNA hybridization/polymorphism, and motor rotation dynamics. The above systematic investigations emphasize the importance and unique advantages of universal single-molecule electrical approaches for realizing direct, label-free, real-time electrical measurements of reaction dynamics with single-event sensitivity. These approaches promise a fascinating mainstream platform to explore the dynamics of stochastic processes in chemical/biological systems as well as gain information in fields ranging from reaction chemistry for elucidating the intrinsic mechanisms to genomics or proteomics for accurate molecular and even point-of-care clinical diagnoses.

Robust graphene-based molecular devices.

One of the main challenges to upscale the fabrication of molecular devices is to achieve a mechanically stable device with reproducible and controllable electronic features that operates at room temperature1,2. This is crucial because structural and electronic fluctuations can lead to significant changes in the transport characteristics at the electrode-molecule interface3,4. In this study, we report on the realization of a mechanically and electronically robust graphene-based molecular junction. Robustness was achieved by separating the requirements for mechanical and electronic stability at the molecular level. Mechanical stability was obtained by anchoring molecules directly to the substrate, rather than to graphene electrodes, using a silanization reaction. Electronic stability was achieved by adjusting the π-π orbitals overlap of the conjugated head groups between neighbouring molecules. The molecular devices exhibited stable current-voltage (I-V) characteristics up to bias voltages of 2.0 V with reproducible transport features in the temperature range from 20 to 300 K.

Antimonene nanosheet device for detection of explosive vapors – A first-principles inspection

The recent advances in the molecular device fabrication have outstretched the exciting applications in vapor sensing devices. This report investigates the explosive vapor detection using the antimonene molecular device (AMD) implemented with the first-principles study. The adsorption of four different explosive vapors namely hexanitrostilbene, M-dinitrobenzene, picric acid, and 2,4,6-trinitrotoluene on AMD device is examined. The adsorption configurations, charge transfer, band gap variation of antimonene nanosheet upon adsorption of explosive vapors on AMD are studied. The adsorption of vapors on AMD device is supported with the transmission spectrum and current-voltage features. Further, the results suggest that next-generation nanosensor is conceivable using antimonene nanosheets.

Effect of electrode position and cross section size on transport properties of molecular devices

Many investigations indicate that molecular electronics opens up possibilities for continually miniaturizing the electronic devices beyond the limits of the standard silicon-based technologies. There have been significant experimental and theoretical efforts to build molecular junctions and to study their transport properties. The electron transport in molecular device shows clearly quantum effect, and the transport property for molecular device would be strongly affected by chemical and structural details, including the contact position and method between molecule and electrodes, the angle between two electrodes connecting to the molecule. Till now, the micro-fabrication technology still does not guarantee metal electrodes contacting the molecules surfaces ideally. During molecular device fabrication, any tiny variations for the contact configuration usually exist in the molecular device, which would change the device transport property. Hence, it is necessary to investigate the effects of electrode position and electrode cross section size on the transport property.We take Au-benzene-1, 4-dithiol (BDT)-Au (Au-BDT-Au) molecular junctions as example, and systematically calculate its transport properties with various contact positions, and several electrode cross section sizes. The contact face for Au electrode is set to be the (001) face. In the calculations, the density functional theory combined with the Keldysh non-equilibrium Green's function formalism is utilized. The local density approximation is selected as an exchange correlation potential, and atomic core is determined by the standard norm conserving nonlocal pseudo-potential.Our investigations show that the relative position between the electrodes plays a crucial role in the transport behavior of Au-BDT-Au device. When both electrodes are set to be at the counter-position, the preferable transport behavior could be found. The counter-position indicates that the two electrodes are on the same line, which is beneficial to the fabrication. As the angle, which is defined as the angle of electrode deviating from the axis, is larger than five degrees, the transport behavior deteriorates. Hence, the angle for the electrode deviating from its axis should be less than five degrees. To study the effect of electrode cross section size, we calculate the transport properties for three electrode cross sections, i.e. 3×4, 4×4 and 5×4 supercell. Our calculations indicate that when electrode cross section is less than 4×4, the transmission, near the Fermi level, is discontinuous, which would deteriorate the transport performance. Hence, the section size of electrode should not be less than 4×4. This research will provide a scientific index for the electrode position and its cross section size during the fabrication.

A Facile Supramolecular Approach towards Strategic Fluorescence Switching and Recognition‐Controlled Photoreduction

AbstractA supramolecular system design strategy to control photoreduction is reported. 1,4,5,8‐naphthalenediimide (NDI) was used as the core unit to synthesize two different sets of ionic aromatic amphiphiles (AA), one incorporating the NDI with an aliphatic chain (denoted NDI) and the other with a phenoxy‐based chain (denoted NDI‐Phe). These systems form self‐assembled structures which are different to those in their monomeric states and which can selectively be photoreduced to generate the radical anion (NDI‐Phe.−) and dianion (NDI2−) in the presence of dicarboxylic acids as the counter anion (CA). Interestingly, fluorescence (FL) switching was detected in the different redox states. The reduction mechanisms and the kinetics were found to be different for these two sets of AAs and the reduction kinetics were further controlled by the structurally different CAs. This unexpected observation reveals molecular recognition in the controlled‐assembly systems. The changes in spectroscopic output upon an electronic input have been described as a simple “off/on” FL switch. The appealing “bottom‐up” approach toward molecular device fabrication is possible only in molecular assembly systems such as these.

Single-Atom Switches and Single-Atom Gaps Using Stretched Metal Nanowires.

Utilizing individual atoms or molecules as functional units in electronic circuits meets the increasing technical demands for the miniaturization of traditional semiconductor devices. To be of technological interest, these functional devices should be high-yield, consume low amounts of energy, and operate at room temperature. In this study, we developed nanodevices called quantized conductance atomic switches (QCAS) that satisfy these requirements. The QCAS operates by applying a feedback-controlled voltage to a nanoconstriction within a stretched nanowire. We demonstrated that individual metal atoms could be removed from the nanoconstriction and that the removed metal atoms could be refilled into the nanoconstriction, thus yielding a reversible quantized conductance switch. We determined the key parameters for the QCAS between the "on" and "off" states at room temperature under a small operating voltage. By controlling the applied bias voltage, the atoms can be further completely removed from the constriction to break the nanowire, generating single-atom nanogaps. These atomic nanogaps are quite stable under a sweeping voltage and can be readjusted with subangstrom accuracy, thus fulfilling the requirement of both reliability and flexibility for the high-yield fabrication of molecular devices.

Addressing the Challenges of Using Ferromagnetic Electrodes in Molecular Devices

ABSTRACTFerromagnetic (FM) electrodes chemically anchored with thiol functionalized molecules can yield novel molecular spintronics devices (MSDs). However, significant challenges lie in developing commercially viable MSD fabrication approach utilizing FM electrodes. A practical MSD fabrication approach should consider FM electrodes’ susceptibility to oxidation, chemical etching, and stress induced deformations during fabrication and usage. This paper will discuss NiFe, an alloy used in the present day memory devices and high-temperature engineering applications, as a candidate for FM electrode and for the fabrication of MSDs. Our spectroscopic reflectance studies show that NiFe starts oxidizing aggressively beyond ∼90 ⁰C. The NiFe surfaces, aged for several months or heated for several minutes below ∼90 ⁰C, were suitable for chemical bonding with the thiol-functionalized molecules. NiFe also demonstrated excellent etching resistance in widely used dichloromethane solvent for dissolving molecular device elements. NiFe also reduced the mechanical stress induced deformities in other FM metals like cobalt. This paper also discusses the successful utilization of NiFe electrodes in the magnetic tunnel junction based molecular device fabrication approach. This research is expected to address the knowledge gap blocking the experimental development of FM based MSDs.

The optical characterization of metal-mediated aggregation behaviour of amphiphilic Zn(ii) phthalocyanines.

Ag(+) mediated aggregation behaviour of two different amphiphilic zinc phthalocyanines (Zn-Pcs) (symmetric and asymmetric) has been investigated in solution, at the air-water interface and in Langmuir-Blodgett (LB) films transferred onto glass substrates. A 4 : 1 ([Ag(+)]/[Pc]) complexation was observed for both symmetric and asymmetric Zn-Pcs at high [Ag(+)] concentrations which led to the formation of H-aggregates in solution. At the air-water interface, both symmetric and asymmetric Zn-Pcs showed a tilted, edge-on orientation in columnar stacks. Addition of Ag(+) to the subphase enhanced the order in the monolayers. LB films on glass substrates showed a split Q-band indicating the presence of "herring-bone" type aggregation consisting of both H- and J-aggregates. For LB films deposited from a Ag(+) containing subphase, a shoulder appeared in the absorption spectra at longer wavelengths which indicates that the fraction of J-aggregates was enhanced by Ag(+) in LB films. The molecular orientation in LB films was investigated by polarized absorption spectroscopy and a tilt angle was calculated to be 49° with the substrate normal for symmetric and 74.6° for the asymmetric Zn-Pc. The presence of Ag(+) cations in the subphase decreased the tilt angles slightly by 4-5°. These results indicate that Ag(+) induced the aggregation of Zn-Pcs and acted as a linker between Pc molecules in the ultrathin films of both symmetric and asymmetric Zn-Pcs. These results are important in inducing J-aggregates for the fabrication of molecular devices based on phthalocyanine thin films.

Addressing the challenges of using ferromagnetic electrodes in the magnetic tunnel junction-based molecular spintronics devices

Ferromagnetic electrodes chemically bonded with thiol functionalized molecules can produce novel molecular spintronics devices. However, major challenges lie in developing Ferromagnetic electrodes based commercially viable device fabrication scheme that consider the susceptibility of ferromagnetic electrodes to oxidation, chemical etching, and stress induced deformations during fabrication and usage. This paper studies NiFe, an alloy used in the present day memory devices and high-temperature engineering applications, as a candidate FM electrode for the fabrication of MSDs. Our spectroscopic reflectance studies show that NiFe start oxidizing aggressively beyond 90 C. The NiFe surfaces, aged for several months or heated for several minutes below 90 C, exhibited remarkable electrochemical activity and were suitable for chemical bonding with the thiol functionalized molecular device elements. NiFe also demonstrated excellent etching resistance and minimized the mechanical stress induced deformities. This paper demonstrates the successful utilization of NiFe electrodes in the tunnel junction based molecular device fabrication approach. This paper is expected to fill the knowledge gap impeding the experimental development of ferromagnetic electrode based molecular spintronics devices for realizing novel logic and memory devices and observing a numerous theoretically predicted phenomenon.

Advantages of Prefabricated Tunnel Junction-Based Molecular Spintronics Devices

Molecule-based devices may govern the advancement of the next generation's logic and memory devices. Molecules have the potential to be unmatched device elements as chemists can mass produce an endless variety of molecules with novel optical, magnetic and charge transport characteristics. However, the biggest challenge is to connect two metal leads to a target molecule(s) and develop a robust and versatile device fabrication technology that can be adopted for commercial scale mass production. This paper discusses distinct advantages of utilizing commercially successful tunnel junctions as a vehicle for developing molecular spintronics devices. We describe the use of a prefabricated tunnel junction with the exposed sides as a testbed for molecular device fabrication. On the exposed sides of a tunnel junction molecules are bridged across an insulator by chemically bonding with the two metal electrodes; sequential growth of metal–insulator–metal layers ensures that separation between two metal electrodes is controlled by the insulator thickness to the molecular device length scale. This paper highlights various attributes of tunnel junction-based molecular devices with ferromagnetic electrodes for making molecular spintronics devices. We strongly emphasize a need for close collaboration between chemists and magnetic tunnel junction (MTJ) researchers. Such partnerships will have a strong potential to develop tunnel junction-based molecular devices for futuristic areas such as memory devices, magnetic metamaterials, high sensitivity multi-chemical biosensors, etc.