1. Introduction
The study of the effects of mixing a conducting polymer with bi-stable spin crossover (SCO) molecular complexes is fairly recent and sparse [1,2,3,4,5,6,7,8,9]. Efforts have been made in an attempt to lower the on-state resistance of spin crossover molecular films by forming composites with various conducting polymers [1,3,4,6], largely with the goal of improving the utility of SCO film-based devices [4,10,11,12,13,14,15,16,17,18,19,20]. A previous study of a polymeric spin crossover [Fe(Htrz)2(trz)](BF)4 plus the conducting polymer polyaniline (PANI) showed a reduction in the hysteresis width in the versus T, which is an indication of a reduced cooperative effect [5]. However, the cooperative effect of [Fe(Htrz)2(trz)](BF)4 was restored and enhanced following the addition of iron magnetite (Fe3O4) nanoparticles into the [Fe(Htrz)2(trz)](BF)4 plus PANI composite. This was understood to be due to the phase separation of [Fe(Htrz)2(trz)](BF)4 in the PANI matrix caused by the addition of Fe3O4 nanoparticles. Such a phase separation turned the miscible [Fe(Htrz)2(trz)](BF)4 plus PANI composite into immiscible domains of [Fe(Htrz)2(trz)](BF)4 and PANI, where the Fe3O4 nanoparticles are preferentially segregated to the [Fe(Htrz)2(trz)](BF)4 domains. Overall, the prior study has suggested that the miscibility gap in the SCO-polymer system could be easily perturbed.
Similarly, the spin crossover complex Fe(phen)2(NCS)2 has been much studied [21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41], and the spin state transition temperature for this complex is in the vicinity of 176 K [27,28,29,30,31,32,33,34,37,38,39]. Prior studies of Mn-doped and Zn-doped Fe(phen)2(NCS)2 thin films [38,39,40], as well as [Fe(phen)2(NCS)2] crystallites coated with an organic, like glycerol [41], showed that the hysteresis width, in versus T, varied depending on the dopant [38,39] and the coating layer [41], respectively. In this study, we observed that for Fe(phen)2(NCS)2 plus PANI plus varying concentrations of Fe3O4 nanoparticle composites, the hysteresis width of versus T remains largely unchanged. The hysteresis width behavior of Fe(phen)2(NCS)2 plus PANI plus varying concentrations of Fe3O4 nanoparticles is starkly different from that of the [Fe(Htrz)2(trz)](BF)4 plus PANI plus Fe3O4 nanoparticles (1% loading by weight) [5], indicating that the dispersion of a spin crossover complex in PANI and the exchange between the spin crossover complex and the Fe3O4 nanoparticles, which is mediated by PANI, depends very much on the choice of spin crossover molecule. With this work, there are now examples of both ferromagnetic [5] and antiferromagnetic coupling between a spin crossover molecular complex and iron magnetite nanoparticles, mediated by polyaniline.
2. Experimental Details
All the reagents and solvents were used as received. Ammonium iron (II) sulfate hexahydrate (99%), aniline (99.8%), ammonium persulfate (APS), and hydrochloric acid (HCl) (ACS reagent, 37%) were purchased from Fisher Scientific (Hampton, NH, USA). 1–10 phenanthroline monohydrate was purchased from Chem-Impex (Wood Dale, IL, USA). Sodium thiocyanate (NaSCN) (99%) was purchased from Avantor (Radnor Township, PA, USA). Ethanol and methanol (≥99.9%) were purchased from Aldrich (St. Louis, MO, USA). Iron (II, III) nano-powders (50–100 nm particle size, 97% trace metals) were purchased from Millipore Sigma (Burlington, MA, USA). The solutions used in this study were made with deionized (DI) water purified through a Millipore Synergy system (18.2 MΩ·cm, Millipore, Billerica, MA, USA).
The method used for the synthesis of Fe(phen)2(NCS)2 was adapted from the one used by Akabori et al. [42]. In brief, 1.95 g of ammonium iron (II) sulfate hexahydrate and 3.00 g of 1–10 phenanthroline were dissolved together in 200 mL of DI water, resulting in a dark-red solution. Next, 21 g of NaSCN was added to 15 mL of DI water to create a saturated solution, and this solution was added to the dark-red solution while stirring. Fine crystals were observed immediately, but the solution mixture was stirred for another four hours at room temperature to complete the reaction. The crude product was collected on Whatman filter paper and rinsed with methanol. It was further purified via recrystallization in methanol and dried in air. The purity was determined by IR spectroscopy (Supplementary Materials Figure S1).
The synthesis of PANI was adapted from the methods used by Tang et al. [43] and Adams et al. [44]. A solution containing 0.25 M aniline (683 µL) in 30 mL of DI water was placed in an ice bath with magnetic stirring at 800 rpm, and 0.25 M APS in 10 mL of 1 M HCl was added to the aniline solution. The solution was allowed to stir for six hours at 0 °C. A dark green precipitate began to form within the first half hour. After six hours, the reaction was left to proceed overnight with stirring at room temperature. The dark green precipitate was collected using ultracentrifugation at 4500 rpm for 30 min and washed several times with 1 M HCl, ethanol, and DI water.
The fabrication of the composite thin films of Fe(phen)2(NCS)2 plus PANI and Fe(phen)2(NCS)2 together with PANI and Fe3O4 nanoparticles was accomplished through a solvent approach. In total, 20 mg of Fe(phen)2(NCS)2 and 20 mg of PANI were added to 5 mL of methanol, and this mixture was sonicated in a Branson 2510R-MT bath sonicator at room temperature for 10 min to create a uniform dispersion. This mixture, also known as the 1:1 Fe(phen)2(NCS)2/PANI bi-composite, was then dried to completion in air prior to vibrating sample magnetometry (VSM) analysis. The 1:1 Fe(phen)2(NCS)2/PANI bi-composite ratio is emphasized in this work to make the comparison with the prior study of the [Fe(Htrz)2(trz)](BF)4 plus PANI composite [5] more facile. To fabricate the tri-composite samples containing Fe(phen)2(NCS)2, PANI, and Fe3O4, different amounts (1, 5, and 10% by weight) of Fe3O4 nanoparticles were added to the 1:1 Fe(phen)2(NCS)2/PANI bi-composite and sonicated again for 10 min until uniformly dispersed. These samples were dried in air prior to VSM analysis.
The measurements of DC magnetic susceptibility times temperature () were carried out in DynaCool PPMS from Quantum Design. The elemental mapping of iron and sulfur in the [Fe(phen)2(NCS)2] and its composites was performed using the FEI Tecnai Osiris S/TEM with the means of energy-dispersive X-ray spectroscopy (EDAX) and high-angle annular dark-field imaging mode with a 200 kV accelerating voltage of scanning transmission electron microscopy (HAADF-STEM). The Fe(phen)2(NCS)2 and its composites plus polyaniline (PANI) plus various concentrations of Fe3O4 nanoparticle solutions were drop-casted on formvar/carbon 200 mesh copper TEM grids from Ted Pella.
The room temperature DC current-voltage I(V) measurements of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 (10% loading by weight) drop-cast between two copper electrodes were taken using the two-point probe method and recorded using a 4200A SCS parameter analyzer connected to a Lakeshore cryogenic probe station. The measurements were carried out in the absence of visible light illumination and a sweep rate of 260 ms per data point.
The coupling between the Fe(phen)2(NCS)2 and Fe3O4 nanoparticles in the composite was probed with X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism spectroscopy (XMCD), as a function of temperature, at the Advanced Light Source (Lawrence Berkeley National Laboratory) beamline 6.3.1, with a constant circularly polarized light whose estimated degree of polarization was 0.66. Throughout the experiments, the XAS spectra were taken in the total electron yield mode across the Fe edges ranging from 700 eV to 735 eV with an alternating magnetic field of T, which are anti-parallel () and parallel () with respect to the helicity of the incoming photon. The XMCD signal was later evaluated as a difference of the two XAS spectra taken with two oppositely applied magnetic fields.
3. Miscibility and Cooperativity
The intermolecular interactions, namely the cooperative effects [45,46,47,48], were examined through thermal hysteresis in terms of the magnetic susceptibility () times temperature versus temperature, i.e., the hysteresis width in the plot of versus T. The hysteresis width, in principle, is a measure of the strength of the cooperativity between adjacent SCO molecules, with a larger hysteresis width equivalent to stronger cooperative effects [45,46,47,48]. The hysteresis widths in the versus T for Fe(phen)2(NCS)2 and for the combination of Fe(phen)2(NCS)2 plus PANI were 10.6 K and 11.3 K, respectively, as shown in Figure 1 (Supplementary Figure S4). The percentage error in the measured versus T hysteresis width was less than 6%. The observed hysteresis width in this study is significantly larger than the 0.15 to 1.5 K [27,29,30,33,34] and 6.1–8.5 K [31] reported previously but roughly similar to the hysteresis width of Mn-doped and Zn-doped Fe(phen)2(NCS)2 thin films, which were 10 K [39] and 14 K [38]. This is surprising as this is very different from the example of [Fe(Htrz)2(trz)](BF)4, where a significant 7 K reduction of versus T hysteresis width was observed upon mixing with PANI [5].
A comparison of the mixtures of Fe(phen)2(NCS)2 with PANI in the ratios of 1:2, 1:1, and 2:1, as seen in Figure 2, illustrates that the magnetization for the Fe(phen)2(NCS)2 to PANI in the ratio of 1:1 is slightly larger than that seen for the ratios of 1:2 and 2:1 Fe(phen)2(NCS)2 to PANI compositions. The temperature-dependent hysteresis varies only slightly, with the hysteresis loop (ΔT1/2) for both the 1:1 Fe(phen)2(NCS)2 to PANI and the 1:2 Fe(phen)2(NCS)2 to PANI bi-composite measuring ~11 K, but for the 2:1 Fe(phen)2(NCS)2 to PANI bi-composite, the hysteresis is ~12 K.
From the elemental mapping of both iron and sulfur of the [Fe(phen)2(NCS)2] in the pristine Fe(phen)2(NCS)2 crystallites and the Fe(phen)2(NCS)2 plus PANI composite, respectively, in Figure 3 and Figure 4, the fact that the Fe(phen)2(NCS)2 is uniformly distributed within the PANI matrix is clear. In other words, there is a high degree of miscibility of Fe(phen)2(NCS)2 within the PANI matrix. The two different spin crossover complexes, [Fe(Htrz)2(trz)](BF)4 and Fe(phen)2(NCS)2, while both are apparently miscible with the PANI, do not mix the same way in the PANI, judging from the differences in the changes to the hysteresis width in the versus T seen with mixing [Fe(Htrz)2(trz)](BF)4 with PANI and not seen when Fe(phen)2(NCS)2 was mixed with PANI, as noted above. One notable difference between these two spin crossover molecules is that [Fe(Htrz)2(trz)](BF)4 is a polymeric spin crossover complex and Fe(phen)2(NCS)2 is not.
We offer two possible explanations as to why the cooperative effects (as indicated by the temperature-dependent hysteresis of the susceptibility) of Fe(phen)2(NCS)2 moieties mixed in the PANI remain largely unchanged. First, there could exist tiny Fe(phen)2(NCS)2 crystallites with the correct packing for enhancing the hysteresis [31] that are evenly distributed within the PANI matrix. For Fe(phen)2(NCS)2, the hysteresis width can also be affected by the crystallite quality [31,34]. Alternatively, there is the possibility of strong cooperativity between Fe(phen)2(NCS)2 moieties in widely distributed crystallites or PANI, which enhances the versus T hysteresis observed in this study here. The large and unperturbed versus T hysteresis suggests that PANI encapsulates the Fe(phen)2(NCS)2, which could enhance the overall cooperativity. Similar polymer-encapsulation-induced hysteresis enhancement of [Fe(phen)2(NCS)2] has been reported [25,41]. The explanation is consistent with the observations where there is strong cooperativity for Fe(phen)2(NCS)2 when encapsulated by organics [7,9,25,41]. The latter explanation is consistent with the observed increased hysteretic spin transition behavior of Fe(phen)2(NCS)2 in several different embedding matrices [9].
4. Phase Separation and Cooperativity
With increasing Fe3O4 nanoparticle concentrations in the Fe(phen)2(NCS)2 plus PANI composite, the Fe3O4 nanoparticles tend to agglomerate and become less uniformly distributed (Figure 5b, Figure 6b and Figure 7b) in the PANI matrix, while the Fe(phen)2(NCS)2 remains uniformly distributed within the PANI, as indicated by the sulfur spatial map (Figure 5c, Figure 6c and Figure 7c). Although there is always a possibility that the coupling between the Fe3O4 nanoparticles could lead to magnetic frustration, this is excluded here as the overall paramagnetic susceptibility scales with the Fe3O4 nanoparticle concentration in the Fe(phen)2(NCS)2 plus PANI composite.
As shown in Figure 8, the addition of Fe3O4 nanoparticles to the Fe(phen)2(NCS)2 plus PANI composite leads to an increasing paramagnetic susceptibility background with an increasing concentration of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite. In general, as shown in Figure 8, the paramagnetic susceptibility at a fixed temperature is linearly proportional to the concentration of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite.
The hysteresis width in the versus T remains remarkably consistent, with changes no more than 2 K across varying concentrations of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite (Figure 8, Supplementary Materials Table S1, Figures S2 and S3). These largely consistent hysteresis widths indicate that the cooperative effect seen for Fe(phen)2(NCS)2 is stable and remains unperturbed upon mixing with the PANI and the addition of Fe3O4 nanoparticles into the composite. This differs from the doped Fe(phen)2(NCS)2 thin film [38,39], where Mn doping has a profound effect on the hysteresis width in the temperature.
Above the spin state transition temperature, Fe(phen)2(NCS)2 has a significant magnetic moment that can overwhelm the moment from the Fe3O4 nanoparticles at very low Fe3O4 nanoparticle concentrations, as shown in the insets in Figure 9 and Figure 10. For the Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticle (1% loading by weight) composite, there is an increase in the XMCD signal at the Fe 2p core edges (Figure 10) as the Fe(phen)2(NCS)2 goes from the diamagnetic low spin state (at 80 K) to the paramagnetic high spin state (at 300 K). At higher Fe3O4 nanoparticle concentrations in the Fe(phen)2(NCS)2 plus PANI composite, the effect of the Fe(phen)2(NCS)2 spin state is more complex.
The XMCD response, Figure 10a, extracted from the XAS spectra (the insets in Figure 9 and Supplementary Materials Figures S5–S8) with oppositely applied magnetic fields does increase with increasing Fe3O4 nanoparticle concentrations when Fe(phen)2(NCS)2 is in the diamagnetic low spin state (at 80 K). The increase in the XMCD signal is not linear with respect to the increasing Fe3O4 nanoparticle concentration (Figure 11a). This is true even for Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite at 80 K, where Fe(phen)2(NCS)2 is in a low spin state (diamagnetic) and does not contribute to the net magnetization. The surmise is that the Fe3O4 nanoparticles are the primary overall XMCD signal source when Fe(phen)2(NCS)2 is in a low spin state. This hypothesis that the Fe3O4 nanoparticles are the primary overall XMCD signal source when Fe(phen)2(NCS)2 is in a low spin state is consistent with the fact that below the spin crossover transition temperature (<172 K), the magnetic susceptibility is fairly constant in temperature. The non-linear increase in the XMCD signal with respect to the increasing concentrations of Fe3O4 nanoparticles can be attributed to the fact that the agglomeration of Fe3O4 nanoparticles (Figure 4b, Figure 5b and Figure 6b) is ferromagnetically coupled with the Fe(phen)2(NCS)2 in the Fe(phen)2(NCS)2 plus PANI composite, as the Fe3O4 nanoparticles aggregate.
Despite the fact that the magnetic susceptibility times temperature, , at a constant temperature of 210 K increases linearly with respect to an increasing concentration of the Fe3O4 nanoparticles, as shown in Figure 9, a comparison of the XMCD signal at the Fe L3 (2p3/2) edge in Figure 10b provides evidence that there is anti-ferromagnetic coupling between the Fe3O4 nanoparticles and the Fe(phen)2(NCS)2 in the Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles composite. Hence, there is an overall reduction in the XMCD signal (Figure 10b, Supplementary Figure S8), with an increasing concentration of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite when the [Fe(phen)2(NCS)2] is in a high spin state. The decrease in the XMCD response is rather significant, and, therefore, the antiferromagnetic coupling between both the Fe(phen)2(NCS)2 and the Fe3O4 nanoparticles cannot be restricted to only the Fe(phen)2(NCS)2 at the surface of the Fe3O4 nanoparticles. Furthermore, it implies that Fe(phen)2(NCS)2 retains nontrivial paramagnetic correlation lengths in PANI.
5. I(V) Characteristics
The transport measurements also suggest that the behavior of Fe(phen)2(NCS)2 in the composites of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 is not perturbed by the addition of Fe3O4 nanoparticles. The room temperature DC current-voltage I(V) measurement shown in Figure 12 is, in fact, characteristic of the transport behavior of Fe(phen)2(NCS)2 by itself [21], which was carried out on thin films of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 (10% loading by weight) drop-casted between two copper electrodes on a glass substrate without light illumination. As anticipated from the transport behavior of Fe(phen)2(NCS)2 by itself [21], the transport characteristic is Ohmic with a linear slope of 1.02, as plotted in the double log I(V) curve, Figure 12b, approximately below 0.6 V. Above 0.6 V, the transport characteristic remains linear with a slope of 1.38, which is an indication that it tends towards a space charge-limited current regime. Such space charge-limited current behavior of the Fe(phen)2(NCS)2 thin film itself has been reported previously with a linear slope of 2.04 [21]. The slope of 1.38 obtained in this study can be understood as a diminishing of the space charge with Fe(phen)2(NCS)2 in the PANI matrix. This further confirms that mixing Fe(phen)2(NCS)2 with the PANI, which is nominally a conducting polymer, reduces the overall on-state resistance.
We can understand part of this overall behavior, i.e., the diminishing of the space charge, when different concentrations of Fe3O4 nanoparticles are added to the Fe(phen)2(NCS)2 plus PANI composite by noting that Fe(phen)2(NCS)2 remains uniformly mixed with PANI, at least on the scale of the scanning TEM, but as the concentration of Fe3O4 nanoparticles increases, the Fe3O4 nanoparticles are phase separated, as seen in Figure 4, Figure 5 and Figure 6.
6. Summary
The cooperative effect, in general, is sensitive to the sample synthesis method [9,29,31,34,42]. Here, the hysteretic behavior of Fe(phen)2(NCS)2 is larger than generally observed. Yet the large hysteretic behavior of approximately 10 to 11 K is largely retained upon the addition of PANI and Fe3O4 nanoparticles, unlike what was observed with [Fe(Htrz)2(trz)](BF)4 combined with PANI [5] and Mn-doped Fe(phen)2(NCS)2 [38,39]. At the same time, the cooperative effect in this study is among the largest of those reported in the literature [27,28,29,30,31,32,33,34], although it is smaller than the 14 K inferred from [38]. While small groupings of Fe(phen)2(NCS)2 moieties may occur in the PANI matrix, there is no phase separation of the Fe(phen)2(NCS)2 from the PANI. In other words, the Fe(phen)2(NCS)2 tends to mix fairly homogeneously with the PANI.
The agglomeration of Fe3O4 nanoparticles, which is an indication of the phase separation of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite, is observed and it is observed to be directly proportional to the concentration of Fe3O4 nanoparticles. However, the Fe(phen)2(NCS)2 spin crossover molecules remain uniformly distributed within the PANI in all cases, which suggests that there exists a relatively high degree of miscibility.
Surprisingly, adding varying concentrations of Fe3O4 nanoparticles into the Fe(phen)2(NCS)2 plus PANI composite did not perturb the cooperativity. The hysteresis width in the versus T for Fe(phen)2(NCS)2, at the spin state transition, remains consistent, with a hysteresis width change of less than 2 K throughout various concentrations of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite. In addition, from the XMCD at the Fe edges, we observed that the overall XMCD signal does not increase in a linear fashion with respect to an increasing concentration of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite. In addition, the phase-separated Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite tend to exhibit antiferromagnetic coupling between the nanoparticles and Fe(phen)2(NCS)2 when the latter is in the high spin state. The quenching of the XMCD signal with as much as 10% (loading by weight) of the Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite suggests that a considerable volume of Fe(phen)2(NCS)2 in the PANI is antiferromagnetically coupled to the Fe3O4.
Sample Preparation: B.T. and W.K.C.; Data Acquisition: W.K.C., B.T., M.Z.Z., A.S., G.V. and A.T.N.; Data Analysis: B.T., R.Y.L., P.A.D. and W.K.C.; Data Curation: W.K.C., R.Y.L., A.T.N. and P.A.D.; Manuscript Preparation: W.K.C. and P.A.D.; Final Manuscript Preparation: W.K.C., R.Y.L. and P.A.D.; Project Supervision: A.T.N., R.Y.L. and P.A.D.; Funding: R.Y.L. and P.A.D. All authors have read and agreed to the published version of the manuscript.
The Data will gladly be made available upon request.
The research was performed in part at the Nebraska Nanoscale Facility: National Nanotechnology Coordinated Infrastructure which supported by the National Science Foundation under Award No. ECCS: 1542182.
The authors declare that they have no known competing financial or personal relationships with other people or organizations that could inappropriately influence (bias) their work.
Footnotes
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![View Image - Figure 1. The enlarged view of the magnetic susceptibility time temperature, [Forumla omitted. See PDF.], versus [Forumla omitted. See PDF.] plot for Fe(phen)2(NCS)2 crystallites (gray) and its composite Fe(phen)2(NCS)2 plus PANI (1:1 Fe(phen)2(NCS)2/PANI weight %) plotted in red.](https://media.proquest.com/media/hms/THUM/2/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=XtADIrjhoGfWoPy6xe1OAxlhuro%3D "View Image - Figure 1. The enlarged view of the magnetic susceptibility time temperature, [Forumla omitted. See PDF.], versus [Forumla omitted. See PDF.] plot for Fe(phen)2(NCS)2 crystallites (gray) and its composite Fe(phen)2(NCS)2 plus PANI (1:1 Fe(phen)2(NCS)2/PANI weight %) plotted in red.")
Enlarge this image.Figure 1. The enlarged view of the magnetic susceptibility time temperature, [Forumla omitted. See PDF.], versus [Forumla omitted. See PDF.] plot for Fe(phen)2(NCS)2 crystallites (gray) and its composite Fe(phen)2(NCS)2 plus PANI (1:1 Fe(phen)2(NCS)2/PANI weight %) plotted in red.
![View Image - Figure 2. The thermal hysteresis behavior of [Forumla omitted. See PDF.] versus [Forumla omitted. See PDF.] for Fe(phen)2(NCS)2 to PANI bi-composites in the different ratios of 2:1 (green), 1:1 (blue), and 1:2 (orange). The arrows indicate increasing (up) and decreasing (down) temperature paths.](https://media.proquest.com/media/hms/THUM/8/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=hStt%2BjP2H2Z2s0ymAGCuDsn43XU%3D "View Image - Figure 2. The thermal hysteresis behavior of [Forumla omitted. See PDF.] versus [Forumla omitted. See PDF.] for Fe(phen)2(NCS)2 to PANI bi-composites in the different ratios of 2:1 (green), 1:1 (blue), and 1:2 (orange). The arrows indicate increasing (up) and decreasing (down) temperature paths.")
Enlarge this image.Figure 2. The thermal hysteresis behavior of [Forumla omitted. See PDF.] versus [Forumla omitted. See PDF.] for Fe(phen)2(NCS)2 to PANI bi-composites in the different ratios of 2:1 (green), 1:1 (blue), and 1:2 (orange). The arrows indicate increasing (up) and decreasing (down) temperature paths.
![View Image - Figure 3. (a) Image of pristine Fe(phen)2(NCS)2 obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.](https://media.proquest.com/media/hms/THUM/10/sBrGa?_a=ChgyMDI1MDgwNTAyNDgyNzg0NToyMzI5MjESBzEzODMzMjMaCk9ORV9TRUFSQ0giDjIxNi43My4yMTYuMTgwKgcyMDMyMzU1MgozMTE2NzEyMTEwOgtJbmxpbmVJbWFnZUIBMFIGT25saW5lWgNJTEliBFRIVU1qCjIwMjQvMDEvMDFyCjIwMjQvMTIvMzF6AIIBIFAtMTAwMDA4NC0yMDEzOTUtU1RBRkYtbnVsbC1udWxskgEGT25saW5lygFnTW96aWxsYS81LjAgQXBwbGVXZWJLaXQvNTM3LjM2IChLSFRNTCwgbGlrZSBHZWNrbzsgY29tcGF0aWJsZTsgQ2xhdWRlQm90LzEuMDsgK2NsYXVkZWJvdEBhbnRocm9waWMuY29tKdIBElNjaG9sYXJseSBKb3VybmFsc5oCB1ByZVBhaWSqAhtPUzpFTVMtRnVsbFRleHQtZ2V0RnVsbFRleHTKAg9BcnRpY2xlfEZlYXR1cmXiAgFO8gIA%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=N3Q5arxwDZGdJCsgQJ6JIUkqHSw%3D "View Image - Figure 3. (a) Image of pristine Fe(phen)2(NCS)2 obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.")
Enlarge this image.Figure 3. (a) Image of pristine Fe(phen)2(NCS)2 obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.
![View Image - Figure 4. (a) Image of Fe(phen)2(NCS)2 combined with polyaniline (PANI) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.](https://media.proquest.com/media/hms/THUM/12/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=1E2CmEYrrvZyIznvzqhBfp5wJJI%3D "View Image - Figure 4. (a) Image of Fe(phen)2(NCS)2 combined with polyaniline (PANI) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.")
Enlarge this image.Figure 4. (a) Image of Fe(phen)2(NCS)2 combined with polyaniline (PANI) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.
![View Image - Figure 5. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (1% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.](https://media.proquest.com/media/hms/THUM/14/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=ixBLt0G%2FaKdGw5IFL1YbJHS%2FS4Q%3D "View Image - Figure 5. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (1% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.")
Enlarge this image.Figure 5. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (1% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.
![View Image - Figure 6. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (5% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.](https://media.proquest.com/media/hms/THUM/16/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=v9BHX8MmmxxlThSw5HrUFnzK1W8%3D "View Image - Figure 6. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (5% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.")
Enlarge this image.Figure 6. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (5% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.
![View Image - Figure 7. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (10% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.](https://media.proquest.com/media/hms/THUM/18/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=9n8rqSVIvpJgf1HVB4CoYBDAmSo%3D "View Image - Figure 7. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (10% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.")
Enlarge this image.Figure 7. (a) Image of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (10% loading by weight) obtained using scanning transmission microscopy in high-angle annular dark-field mode. (b,c) Elemental mapping of iron and sulfur of the [Fe(phen)2(NCS)2], respectively.
![View Image - Figure 8. The [Forumla omitted. See PDF.] versus T plots for composites of Fe(phen)2(NCS)2 plus PANI plus varying concentrations of Fe3O4 (percent loading, by weight), with an applied magnetic field of 2 T.](https://media.proquest.com/media/hms/THUM/20/sBrGa?_a=ChgyMDI1MDgwNTAyNDgyNzg0NToyMzI5MjESBzEzODMzMjMaCk9ORV9TRUFSQ0giDjIxNi43My4yMTYuMTgwKgcyMDMyMzU1MgozMTE2NzEyMTEwOgtJbmxpbmVJbWFnZUIBMFIGT25saW5lWgNJTEliBFRIVU1qCjIwMjQvMDEvMDFyCjIwMjQvMTIvMzF6AIIBIFAtMTAwMDA4NC0yMDEzOTUtU1RBRkYtbnVsbC1udWxskgEGT25saW5lygFnTW96aWxsYS81LjAgQXBwbGVXZWJLaXQvNTM3LjM2IChLSFRNTCwgbGlrZSBHZWNrbzsgY29tcGF0aWJsZTsgQ2xhdWRlQm90LzEuMDsgK2NsYXVkZWJvdEBhbnRocm9waWMuY29tKdIBElNjaG9sYXJseSBKb3VybmFsc5oCB1ByZVBhaWSqAhtPUzpFTVMtRnVsbFRleHQtZ2V0RnVsbFRleHTKAg9BcnRpY2xlfEZlYXR1cmXiAgFO8gIA%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=JjzqgZJveoB2MEMYDUzrWRs%2F0F0%3D "View Image - Figure 8. The [Forumla omitted. See PDF.] versus T plots for composites of Fe(phen)2(NCS)2 plus PANI plus varying concentrations of Fe3O4 (percent loading, by weight), with an applied magnetic field of 2 T.")
Enlarge this image.Figure 8. The [Forumla omitted. See PDF.] versus T plots for composites of Fe(phen)2(NCS)2 plus PANI plus varying concentrations of Fe3O4 (percent loading, by weight), with an applied magnetic field of 2 T.
![View Image - Figure 9. The value [Forumla omitted. See PDF.] is plotted as a function of the Fe3O4 nanoparticle concentration in Fe(phen)2(NCS)2 plus PANI composite, for T = 210 K. Insets are the X-ray absorption spectra of Fe L3 (2p3/2) and L2 (2p1/2) edges at 80 K (top left corner) and 300 K (bottom right corner) of the Fe(phen)2(NCS)2 plus PANI plus Fe3O4 (1% loading by weight).](https://media.proquest.com/media/hms/THUM/22/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=xtnmh4atKXJ8MyTEeDBQyFiJPl0%3D "View Image - Figure 9. The value [Forumla omitted. See PDF.] is plotted as a function of the Fe3O4 nanoparticle concentration in Fe(phen)2(NCS)2 plus PANI composite, for T = 210 K. Insets are the X-ray absorption spectra of Fe L3 (2p3/2) and L2 (2p1/2) edges at 80 K (top left corner) and 300 K (bottom right corner) of the Fe(phen)2(NCS)2 plus PANI plus Fe3O4 (1% loading by weight).")
Enlarge this image.Figure 9. The value [Forumla omitted. See PDF.] is plotted as a function of the Fe3O4 nanoparticle concentration in Fe(phen)2(NCS)2 plus PANI composite, for T = 210 K. Insets are the X-ray absorption spectra of Fe L3 (2p3/2) and L2 (2p1/2) edges at 80 K (top left corner) and 300 K (bottom right corner) of the Fe(phen)2(NCS)2 plus PANI plus Fe3O4 (1% loading by weight).
![View Image - Figure 10. The Fe ([Forumla omitted. See PDF.] and [Forumla omitted. See PDF.] edges) XMCD signals for Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (1%, 5% and 10% loading by weight). Data were taken for Fe(phen)2(NCS)2 in the low spin state (a) at 80 K and Fe(phen)2(NCS)2 in the high spin state (b) at 300 K.](https://media.proquest.com/media/hms/THUM/24/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=lhfecsmI6rzrcjdrpjQpfq9pbJY%3D "View Image - Figure 10. The Fe ([Forumla omitted. See PDF.] and [Forumla omitted. See PDF.] edges) XMCD signals for Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (1%, 5% and 10% loading by weight). Data were taken for Fe(phen)2(NCS)2 in the low spin state (a) at 80 K and Fe(phen)2(NCS)2 in the high spin state (b) at 300 K.")
Enlarge this image.Figure 10. The Fe ([Forumla omitted. See PDF.] and [Forumla omitted. See PDF.] edges) XMCD signals for Fe(phen)2(NCS)2 plus PANI plus Fe3O4 nanoparticles (1%, 5% and 10% loading by weight). Data were taken for Fe(phen)2(NCS)2 in the low spin state (a) at 80 K and Fe(phen)2(NCS)2 in the high spin state (b) at 300 K.
![View Image - Figure 11. The XMCD signal of the [Forumla omitted. See PDF.] site for varying concentrations (% by weight) of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite at (a) 80 K and (b) 300 K.](https://media.proquest.com/media/hms/THUM/4/sBrGa?_a=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%2BgIBWYIDA1dlYooDHENJRDoyMDI1MDgwNTAyNDgyNzg0NTo4OTc3NjI%3D&_s=HHnJFxelk9kW%2BWkA9OBEIZ5fyYM%3D "View Image - Figure 11. The XMCD signal of the [Forumla omitted. See PDF.] site for varying concentrations (% by weight) of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite at (a) 80 K and (b) 300 K.")
Enlarge this image.Figure 11. The XMCD signal of the [Forumla omitted. See PDF.] site for varying concentrations (% by weight) of Fe3O4 nanoparticles in the Fe(phen)2(NCS)2 plus PANI composite at (a) 80 K and (b) 300 K.
Enlarge this image.Figure 12. (a) The dc I(V) characteristics of Fe(phen)2(NCS)2 plus PANI plus Fe3O4 (10% by weight) and (b) double-log plot of the I(V) characteristics.
Supplementary Materials
The following supporting information can be downloaded at
References
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Details
; Tamang, Binny 2 ; M Zaid Zaz 1
; Subedi, Arjun 1
; Viswan, Gauthami 1
; Alpha T N’Diaye 3
; Lai, Rebecca Y 2
; Dowben, Peter A 1
1 Department of Physics and Astronomy, University of Nebraska-Lincoln, Lincoln, NE 68588, USA;
2 Department of Chemistry, University of Nebraska-Lincoln, Lincoln, NE 68588, USA;
3 Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA;