Solution-processed multiferroic thin-films with large magnetoelectric coupling at room-temperature

Experimental realization of thin films with a significant room-temperature magnetoelectric coupling coefficient, αME, in the absence of an external DC magnetic field, has been thus far elusive. Here, a large coupling coefficient of 750 ± 30 mV Oe-1 cm-1 is reported for multiferroic polymer nanocomposites (MPCs) thin-films in the absence of an external DC magnetic field. The MPCs are based on PMMA-grafted cobalt-ferrite nanoparticles uniformly dispersed in the piezoelectric polymer poly(vinylidene fluoride-co-trifluoroethylene, P(VDF-TrFE). It is shown that nanoparticle agglomeration plays a detrimental role and significantly reduces αME. Surface functionalization of the nanoparticles by grafting a layer of poly(methyl methacrylate) (PMMA) via atom transfer radical polymerization (ATRP) renders the nanoparticle miscible with P(VDF-TRFE) matrix, thus enabling their uniform dispersion in the matrix even in submicrometer thin films. Uniform dispersion yields maximized interfacial interactions between the ferromagnetic nanoparticles and the piezoelectric polymer matrix leading to the experimental demonstration of large αME values in solution-processed thin films, which can be exploited in flexible and printable multiferroic electronic devices for sensing and memory applications.</p

Magnetoelectric coupling coefficient in multiferroic capacitors:Fact vs Artifacts

Multiferroic materials are characterized by their magnetoelectric coupling coefficient, which can be obtained using a lock-in amplifier by measuring the voltage developed across a multiferroic capacitor in a time-variable magnetic field, Hac cos(ωt), where Hac and ω are the amplitude and frequency of the applied magnetic field. The measurement method, despite its simplicity, is subject to various parasitic effects, such as magnetic induction, which leads to significant over-estimation of the actual magnetoelectric response. This article outlines the measurement theory for a multiferroic capacitor using the lock-in technique. It is demonstrated that the inductive contribution has linear proportionality with Hac, ω, and Hacω. It is shown that the true magnetoelectric coupling response is retrieved from the real component of the lock-in signal. Using a polymer-nanoparticle multiferroic composite, the internal consistency of the proposed measurement method is experimentally demonstrated, and it is shown that the actual multiferroic signal can be retrieved using the lock-in technique by removing the magnetic induction contribution from the signal. It is observed that the magnetoelectric voltage shows only a linear dependence with Hac, a saturating behavior with ω, and Hacω. Furthermore, a measurement protocol for reliable reporting of magnetoelectric coupling coefficient has been provided.</p

Solution-processed multiferroic thin-films with large magnetoelectric coupling at room-temperature

Experimental realization of thin films with a significant room-temperature magnetoelectric coupling coefficient, αME, in the absence of an external DC magnetic field, has been thus far elusive. Here, a large coupling coefficient of 750 ± 30 mV Oe-1 cm-1 is reported for multiferroic polymer nanocomposites (MPCs) thin-films in the absence of an external DC magnetic field. The MPCs are based on PMMA-grafted cobalt-ferrite nanoparticles uniformly dispersed in the piezoelectric polymer poly(vinylidene fluoride-co-trifluoroethylene, P(VDF-TrFE). It is shown that nanoparticle agglomeration plays a detrimental role and significantly reduces αME. Surface functionalization of the nanoparticles by grafting a layer of poly(methyl methacrylate) (PMMA) via atom transfer radical polymerization (ATRP) renders the nanoparticle miscible with P(VDF-TRFE) matrix, thus enabling their uniform dispersion in the matrix even in submicrometer thin films. Uniform dispersion yields maximized interfacial interactions between the ferromagnetic nanoparticles and the piezoelectric polymer matrix leading to the experimental demonstration of large αME values in solution-processed thin films, which can be exploited in flexible and printable multiferroic electronic devices for sensing and memory applications.</p

Mechanically stable solution-processed transparent conductive electrodes for optoelectronic applications

The bilayer structure of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) coating on silver nanowires (AgNWs) film is a promising structure for replacing indium tin oxide (ITO) as a flexible transparent conductive electrode. Pristine PEDOT:PSS film due to its hydrophilicity and high permeability cannot fully protect AgNWs from mechanical stress and oxidation. Here, we present a composite approach that improves mechanical properties and lifespan of the AgNWs/PEDOT:PSS electrode by adding polyvinyl alcohol (PVA) as a polymer-surfactant. It is shown that addition of PVA improves the conductivity as well as the stability of hybrid electrode under demanding mechanical stress conditions. The drop in conductivity of the hybrid electrode is only 17% after 2000 repeated bending cycles whereas the reference electrode has shown a dramatic drop of 180% in the conductivity. We speculate that generation of hydrogen bonds between PEDOT:PSS and PVA increases adhesivity and cohesivity of the conductive polymer film to the sublayer. So PEDOT:PSS-PVA film not only fixes the arrangement of AgNWs but also improves the welding on cross junction points. By addition of PVA, optoelectronic performance (Figure-of-merit (ΦTC)) of the electrode is improved from ΦTC = 2.646 × 10-3 Ω-1 for AgNWs/PEDOT:PSS to ΦTC = 3.819 × 10-3 Ω-1 for AgNWs/PEDOT:PSS-PVA electrode and power conversion efficiency (PCE) of the polymer solar cell (PSC) is increased by over 17%.</p

Visible Light-Assisted Photoreduction of Graphene Oxide Using CdS Nanoparticles and Gas Sensing Properties

Graphene oxide sheets suspended in ethanol interact with excited CdS nanoparticles and contributed to photocatalytic reduction by accepting electron from nanoparticle. The UV-Vis measurement showed that electrical absorbance of the CdS/graphene oxide sheets increased by decreasing the irradiation time and after 2 h it remained constant which indicates the optimum reduction time. Furthermore, the direct interaction between CdS nanoparticles and graphene sheets hinders the collapse of exfoliated sheets of graphene. The 4-point probe measurement of nanocomposite with different ratios of graphene oxide in CdS solution after irradiation shows that the conductivity of them increased by increasing the amount of GO, but further increasing causes incomplete photo reduction process due to exorbitance increasing GO sheets which contribute to decreasing the conductivity. The CdS/RGO composite material can be used as a gas sensor for CO2 based on its electrocatalytic behavior. The low-cost and easy fabrication sensor shows rapid response and high sensitivity. By varying the amount of GO the optimum concentration which shows high sensitivity is found and its good performance compared with other is attributed to its higher conductivity due to complete reduction. Moreover, the effects of thermal annealing on the conductivity of CdS/RGO film and the performance of devices are researched

Ultrasound-Mediated Atom Transfer Radical Polymerization for Polymer-Grafted Magnetic Nanoparticles with Controlled Packing Density

Surface-initiated atom transfer radical polymerization (SI-ATRP) is emerging as an innovative surface modification approach for the functionalization of magnetic nanoparticles (MNPs) to improve their colloidal stability, biocompatibility, or enhanced processability and dispersibility inside a polymer matrix. However, nanoparticle agglomeration challenges the applicability of ATRP, particularly of highly interacting systems where interparticle interactions, such as magnetic forces, exacerbate agglomeration and hinder the uniform grafting of polymer chains from individual nanoparticles. Here, we report ultrasound-mediated SI-ATRP (uSI-ATRP), as an innovative solution to address the challenges of agglomeration in strongly interacting MNPs. Through a systematic study of various reaction parameters, it is shown that uSI-ATRP follows first-order reaction kinetics, thus enabling precise control over the molecular weight and polydispersity index (PDI) of the grafted polymeric shell from the surface of MNPs by controlling the reaction time. It is demonstrated that ultrasound mediation prevents nanoparticle agglomeration very efficiently and yields uniform grafting of polymer chains from individual particles. Achieving agglomeration-free dispersion of polymer-grafted MNPs enables the realization of thin films of ferromagnetic nanoparticles with a packing density of >1011 per cm2 using large-area solution processing techniques. This work presents a highly reproducible route to creating well-defined polymer-grafted nanoparticles, even for systems prone to significant interparticle interaction, and opens avenues for the development of novel functional nanomaterials with tailored properties

Solution-Processed Multiferroic Thin-Films with Large Magnetoelectric Coupling at Room-Temperature

Experimental realization of thin films with a significant room-temperature magnetoelectric coupling coefficient, αME, in the absence of an external DC magnetic field, has been thus far elusive. Here, a large coupling coefficient of 750 ± 30 mV Oe–1 cm–1 is reported for multiferroic polymer nanocomposites (MPCs) thin-films in the absence of an external DC magnetic field. The MPCs are based on PMMA-grafted cobalt-ferrite nanoparticles uniformly dispersed in the piezoelectric polymer poly(vinylidene fluoride-co-trifluoroethylene, P(VDF-TrFE). It is shown that nanoparticle agglomeration plays a detrimental role and significantly reduces αME. Surface functionalization of the nanoparticles by grafting a layer of poly(methyl methacrylate) (PMMA) via atom transfer radical polymerization (ATRP) renders the nanoparticle miscible with P(VDF-TRFE) matrix, thus enabling their uniform dispersion in the matrix even in submicrometer thin films. Uniform dispersion yields maximized interfacial interactions between the ferromagnetic nanoparticles and the piezoelectric polymer matrix leading to the experimental demonstration of large αME values in solution-processed thin films, which can be exploited in flexible and printable multiferroic electronic devices for sensing and memory applications