Bio-inspired protonic memristor devices based on metal complexes with proton-coupled electron transfer.

A new type of memristor inspired by bio-membranes is presented, based on the proton movement resulting from proton-coupled electron transfer (PCET) processes in dinuclear Ru complexes, whereby a two-terminal device based on said Ru complexes and a proton-conducting polymer was constructed as a proof-of-concept. Two ITO electrodes were modified separately with dinuclear Ru complexes that bear tetraphosphonic acid linkers at both ends and a 2,6,2',6'-tetrakis(benzimidazol-2-yl)-4,4'-bipyridine (RuNH-OH) or 1,3,1',3'-tetrakis(benzimidazol-2-yl)-5,5'-biphenyl (RuCH-OH) bridging ligand, and both ITO electrodes exhibit PCET processes with different Ru(ii/iii) redox potentials and pKa values. Poly(4-vinylpyridine) (P4VP; pKa = 4-5), a proton-conducting polymer, was sandwiched between the two modified ITO electrodes to construct a two-terminal device of the type ITO|(RuNH-OH)3|P4VP|(RuCH-OH)3|ITO. Initially, the oxidation state of the metal centers in RuNH-OH and RuCH-OH is Ru(ii) and Ru(iii), respectively. Upon applying a bias voltage between the two ITO electrodes, the high and low current states switch at approximately ±1.10 V due to Ru(ii/iii) redox reactions. At the RuNH-OH|P4VP and RuCH-OH|P4VP interfaces, a proton is released from Ru(ii)NH-OH and subsequently captured by Ru(iii)CH-OH through the hydrogen-bonding interaction with the P4VP polymer, which is driven by the changes in the pKa values of the Ru complexes from 4.1-8.8 [Ru(ii)NH-OH] to <3.8 [Ru(iii)NH-OH] and from <8.4 [Ru(ii)CH-OH] to 5.2-9.8 [Ru(iii)CH-OH] under these conditions. The redox reactions on the modified Ru films create a large proton gradient between the two electrodes, enhancing the proton conductivity through the P4VP layer (pKa = 4-5). When the applied bias potential was inverted, the pKa gradient returned to the original state and the current decreased. Such a proton-conductivity enhancement is relevant to the transport of protons by proton gradients in bio-membranes. Therefore, the present protonic coordination-network films containing metal complexes that exhibit PCET should open new avenues for the design of a new type of memristor devices mimicking the function of synapses.

Viral infection induces different detoxification enzyme activities in insecticide-resistant and -susceptible brown planthopper Nilaparvata lugens strains.

This study aimed to describe the relationship between viral infection in Nilaparvata lugens (Stål), the brown planthopper (BPH), and different insecticide susceptibilities. BPH-resistant strains were selected using fenthion (an organophosphate) or etofenprox (a pyrethroid); a susceptible strain was used as the baseline colony before insecticide selection. All strains were infected with rice ragged stunt virus (RRSV) or rice grassy stunt virus (RGSV), after which the activities of three detoxification enzymes, cytochrome-P450-monooxygenase (P450), glutathione S-transferase (GST), and carboxylesterase (CE), were compared. Males of the strains selected for both insecticides showed high P450 and GST-CDNB activities. The activity of all enzymes was higher in males than in females, as a whole. However, males of the susceptible strain infected with RRSV showed decreased CE and GST-CDNB activities. BPH with low susceptibility to etofenprox showed a marked increase in P450 activity after RRSV infection; the GST-CDNB activity of females in the insecticide-resistant strain increased. RGSV infection induced high CE and P450 activities in etofenprox-selected females. The RRSV infection rate, but not the RGSV, decreased in etofenprox-selected strains.

Proton-Rocking-Chair-Type Redox Capacitors Based on Indium Tin Oxide Electrodes with Multilayer Films Containing Ru Complexes.

A rechargeable proton-rocking-chair-type redox capacitor was fabricated using scalable layer-by-layer-(LbL)-assembled films composed of two dinuclear Ru complexes that exhibit proton-coupled electron-transfer (PCET) reactions with different Ru(II/III) redox potentials (RuNH-OH and RuCH-OH). RuNH-OH and RuCH-OH contain different coordination environments that involve two phosphonate linker ligands at both ends and bridging 2,6,2',6'-tetrakis(benzimidazol-2-yl)-4,4'-bipyridine or 1,3,1',3'-tetrakis(benzimidazol-2-yl)-5,5'-biphenyl ligands, respectively. The molecular units were assembled onto indium tin oxide (ITO) electrodes by complexation between the phosphonate groups and zirconium(IV) ions. The LbL growing process of these multilayer films was monitored by electrochemical or UV-vis spectroscopic measurements. The thus obtained LbL films on the ITO electrodes showed PCET reactions at different potentials, depending on the bridging ligands. The introduction of cyclometalated Ru-C bonds in the bridging ligand of RuCH-OH led to the stabilization of the ruthenium(III) oxidation state, and therefore, RuCH-OH exhibited lower p Ka values for the imino N-H protons in the bridging benzimidazole groups compared to those of the corresponding RuNH-OH complex. The proton movements that accompany the redox reaction in the Ru multilayer films on the ITO electrode were confirmed using a pH indicator probe. For the performance test of a proton-rocking-chair-type redox capacitor, a two-electrode system composed of RuNH-OH and RuCH-OH multilayer films on ITO electrodes was examined in an aqueous solution of NaClO4. Under galvanostatic conditions, stable, reversible, and repeatable charging/discharging processes occurred. The capacitance increased with an increasing number of LbL layers. For comparison, a similar redox capacitor composed of two RuNMe-OH and RuCMe-OH analogues, in which all four imino N-H protons on the benzimidazole moieties are protected by N-Me groups, was constructed and examined. In these complexes, the capacitance decreased by 77% compared to the PCET-type capacitor composed of a cell containing RuNH-OH and RuCH-OH; this result strongly suggests that the proton movement plays a more important role for the charge storage than the anion movement. In such LbL films composed of Ru complexes that exhibit PCET-type redox reactions, the capacitance is drastically improved with an increasing number of layers and using protons as charge carriers.

Hydrogen-bonded metallo-supramolecular polymers based on ruthenium or iron complexes for the selective extraction of single-walled carbon nanotubes.

The chemical functionalization of nano-carbon materials such as single-walled carbon nanotubes (SWNTs) and graphene by metal complexes has attracted much attention due to the multitude of potential applications in efficient energy-conversion and -storage devices. The solubilization and single-chirality separation of SWNTs by surface modifications is a useful approach to manipulate SWNTs in the liquid phase. In this study, several Ru and Fe complexes containing two terminal quadruple hydrogen-bonded (H-bonded) ureidopyrimidinedione (UPy) groups were synthesized (Ru-1, Ru-UPy, and Fe-UPy) to form H-bonded supramolecular polymers by self-association. In order to control the solubility of these complexes in nonpolar solvents, Ru-UPy and Fe-UPy were endowed with long alkyl side chain groups in the coordinated 2,6-bis(benzimidazol-2-yl)pyridine ligand, while Ru-1 and Ru-2 do not contain such long alkyl chain groups. AFM measurements revealed that Ru-1, Ru-UPy, and Fe-UPy form a fiber-like network morphology on HOPG surfaces, arising from the H-bonded aggregation. However, only Ru-UPy and Fe-UPy are able to solubilize SWNTs effectively upon simple sonication in chlorobenzene. After the solubilization of a CoMoCAT® SWNT in chlorobenzene using Ru-UPy or Fe-UPy, UV-Vis-NIR spectra showed sharp peaks at 996 and 1150 nm, which were attributed to (6, 5) and (7, 6)-SWNTs. The Raman spectra of the solubilized SWNTs revealed peaks that were attributed to the radial breathing mode (RBM), which suggests an enrichment of semiconducting SWNTs, i.e., Ru-UPy and Fe-UPy are able to selectively solubilize semiconducting SWNTs. Cyclic voltammograms of films of SWNTs covered with Ru-UPy or Fe-UPy on ITO electrodes showed a well-defined adsorbed Ru(ii/iii) or Fe(ii/iii) wave. Upon addition of acid, the redox response from the adsorbed H-bonded Ru-UPy and Fe-UPy disappeared and only SWNTs were left on the ITO electrode. Moreover, the Ru-UPy/SWNT and Fe-UPy/SWNT hybrids exhibited non-linear I-V characteristics.

Energy-Storage Applications for a pH Gradient between Two Benzimidazole-Ligated Ruthenium Complexes That Engage in Proton-Coupled Electron-Transfer Reactions in Solution.

The judicious selection of pairs of benzimidazole-ligated ruthenium complexes allowed the construction of a rechargeable proton-coupled electron-transfer (PCET)-type redox battery. A series of ruthenium(II) and -(III) complexes were synthesized that contain substituted benzimidazoles that engage in PCET reactions. The formation of intramolecular Ru-C cyclometalation bonds stabilized the resulting ruthenium(III) complexes, in which pKa values of the imino N-H protons on the benzimidazoles are usually lower than those for the corresponding ruthenium(II) complexes. As a proof-of-concept study for a solution redox battery based on such PCET reactions, the charging/discharging cycles of several pairs of ruthenium complexes were examined by chronopotentiometry in an H-type device with half-cells separated by a Nafion membrane in unbuffered CH3CN/H2O (1/1, v/v) containing 0.1 M NaCl. During the charging/discharging cycles, the pH value of the solution gradually changed accompanied by a change of the open-circuit potential (OCP). The changes for the OCP and pH value of the solution in the anodic and cathodic half-cells were in good agreement with the predicted values from the Pourbaix diagrams for the pairs of ruthenium complexes used. Accordingly, the careful selection of pairs of ruthenium complexes with a sufficient potential gradient and a suitably large pKa difference is crucial: the charge generated between the two ruthenium complexes changes the OCP and the pH difference between the two cells in an unbuffered solution, given that the PCET reactions occur at both electrodes and that discharging leads to the original state. Because the electric energy is stored as a pH gradient between the half-cells, new possibilities for PCET-type rocking-chair redox batteries arise.

Controlling the Direction of the Molecular Axis of Rod-Shaped Binuclear Ruthenium Complexes on Single-Walled Carbon Nanotubes.

We report the synthesis of a mixed-valence ruthenium complex, bearing pyrene moieties on one side of the ligands as anchor groups. Composites consisting of mixed-valence ruthenium complexes and SWNTs were prepared by noncovalent π-π interactions between the SWNT surface and the pyrene anchors of the Ru complex. In these composites, the long axis of the Ru complexes was aligned in parallel to the principal direction of the SWNT. The optimized conformation of these complexes on the SWNT surface was calculated by molecular mechanics. The composites were examined by UV/Vis absorption and FT-IR spectroscopy, XPS, and SEM analysis. Furthermore, their electrochemical properties were evaluated. Cyclic voltammograms of the composites showed reversible oxidation waves at peak oxidation potentials (Epox ) = 0.86 and 1.08 V versus Fc(+) /Fc, which were assigned to the Ru(II) -Ru(II) /Ru(II) -Ru(III) and the Ru(II) -Ru(III) /Ru(III) -Ru(III) oxidation events of the dinuclear ruthenium complex, respectively. Based on these observations, we concluded that the electrochemical properties and mixed-valence state of the dinuclear ruthenium complexes were preserved upon attachment to the SWNT surface.