We propose novel pseudocapacitors that can store energy related to the partial entropy change associated with proton concentration variations following neutralization reactions. In this situation, it is possible to obtain electrochemical energy after the complete charge/discharge cycle conducted in electrolytic solutions with different proton concentrations. To this end, we prepared modified electrodes from phosphomolybdic acid (PMA), poly(3,4-ethylenedioxythiophene/poly(styrenesulfonate) (PEDOT-PSS), and polyallylamine (PAH) by the layer-by-layer (LbL) method and investigated their electrochemical behavior, aiming to use them in these neutralization pseudocapacitors. We analyzed the potentiodynamic profile of the current density at several scan rates, to evaluate the reversibility of the proton electroinsertion process, which is crucial to maximum energy storage efficiency. On the basis of the proposed reaction mechanism and by using frequency-domain measurements and models, we determined rate constants at different potentials. Our results demonstrated that the conducting polymer affects the self-assembled matrixes, ensuring that energy storage is high (22.5 kJ mol(-1)). The process involved neutralization of a hydrochloric acid solution from pH = 1 to pH = 6, which corresponds to 40% of the neutralization enthalpy.

Layer-by-layer (LbL) nanocomposite films from TiO(2) nanoparticles and tungsten-based oxides (WO(x)H(y)), as well as dip-coating films of TiO(2) nanoparticles, were prepared and investigated by electrochemical techniques under visible light beams, aiming to evaluate the lithium ion storage and chromogenic properties. Atomic force microscopy (AFM) images were obtained for morphological characterization of the surface of the materials, which have similar roughness. Cyclic voltammetry and chronoamperometry measurements indicated high storage capacity of lithium ions in the LbL nanocomposite compared with the dip-coating film, which was attributed to the faster lithium ion diffusion rate within the self-assembled matrix. On the basis of the data obtained from galvanostatic intermittent titration technique (GITT), the values of lithium ion diffusion coefficient (D(Li)) for TiO(2)/WO(x)H(y) were larger compared with those for TiO(2). The rate of the coloration front in the matrices was investigated using a spectroelectrochemical method based on GITT, allowing the determination of the "optical" diffusion coefficient (D(op)) as a function of the amount of lithium ions previously inserted into the matrices. The values of D(Li) and D(op) suggested the existence of phases with distinct contribution to lithium ion diffusion rates and electrochromic efficiency. Moreover, these results aided a better understanding of the temporal change of current density and absorbance during the ionic electro-insertion, which is important for the possible application of these materials in lithium ion batteries and electrohromic devices.

Filmes de quitosana/poli(ácido vinilsulfônico) (PVS) foram depositados sobre membranas de Nafion ® a partir do método camada por camada (LbL), visando o seu uso em células a combustível de metanol direto (DMFC). Métodos computacionais e espectros de infravermelho com transformada de Fourier (FTIR) sugerem a formação de um par iônico entre o grupo sulfônico do PVS e o grupo amino protonado da quitosana, o qual promove o crescimento dos filmes LbL sobre a membrana de Nafion ® , assim como impede parcialmente a passagem de metanol. Experimentos de cronopotenciometria e varredura linear de potencial foram realizados a fim de se investigar a passagem de metanol através das membranas de Nafion ® e quitosana/PVS/Nafion ® em uma célula a diafragma. Os valores de resistência iônica associada ao transporte de prótons nas membranas de Nafion ® e quitosana/PVS/Nafion ® são próximos, de acordo com as medidas de impedância elétrica devido à pequena espessura do filme LbL. Assim, espera-se um melhor desempenho da DMFC, uma vez que a resistência do filme automontado é insignificante comparada ao resultado associado à passagem de metanol através das membranas.Chitosan/poly(vinyl sulfonic acid) (PVS) films have been prepared on Nafion ® membranes by the layer-by-layer (LbL) method for use in direct methanol fuel cell (DMFC). Computational methods and Fourier transform infrared (FTIR) spectra suggest that an ionic pair is formed between the sulfonic group of PVS and the protonated amine group of chitosan, thereby promoting the growth of LbL films on the Nafion ® membrane as well as partial blocking of methanol. Chronopotentiometry and potential linear scanning experiments have been carried out for investigation of methanol crossover through the Nafion ® and chitosan/PVS/Nafion ® membranes in a diaphragm diffusion cell. On the basis of electrical impedance measurements, the values of proton resistance of the Nafion ® and chitosan/PVS/Nafion ® membranes are close due to the small thickness of the LbL film. Thus, it is expected an improved DMFC performance once the additional resistance of the self-assembled film is negligible compared to the result associated with the decrease in the crossover effect.Keywords: chitosan, direct methanol fuel cell, proton exchange membrane, crossover effect, methanol permeability IntroductionDirect methanol fuel cells (DMFCs) are the most promising portable, stationary power sources with application in several fields. In these cells, methanol and air are continually injected into the anode and cathode compartments, respectively, thus providing energy with high efficiency. Methanol has been largely employed as fuel once it is abundant and inexpensive. Even though DMFCs produce carbon dioxide, which is released into the atmosphere, their high efficiency guarantees low pollution as compared to other power sources. [1][2][3] One drawback of DMFCs is the so-called crossover effect, through which methanol leaves the anodic compartment and crosses the proton exchange membrane (PEM), thereby promoting cell de...

One major challenge for the widespread application of direct methanol fuel cells (DMFCs) is to decrease the amount of platinum used in the electrodes, which has motivated a search for novel electrodes containing platinum nanoparticles. In this study, platinum nanoparticles were electrodeposited on layer-by-layer (LbL) films from TiO2 and poly(vinyl sulfonic) (PVS), by immersing the films into a H2PtCl6 solution and applying a 100 microA current during different electrodeposition times. Scanning tunnel microscopy (STM) and atomic force microscopy (AFM) images showed increased platinum particle size and electrode roughness for increasing electrodeposition times. The potentiodynamic profile of the electrodes indicated that oxygen-like species in 0.5 mol L(-1) H2SO4 were formed at less positive potentials for the smallest platinum particles. Electrochemical impedance spectroscopy measurements confirmed the high reactivity for the water dissociation and the large amount of oxygen-like species adsorbed on the smallest platinum nanoparticles. This high oxophilicity of the smallest nanoparticles was responsible for the electrocatalytic activity of Pt-TiO2/PVS systems for methanol electrooxidation, according to the Langmuir-Hinshelwood bifunctional mechanism. Significantly, the approach used here combining platinum electrodeposition and LbL matrices allows one to both control the particle size and optimize methanol electrooxidation, being therefore promising for producing membrane-electrode assemblies of DMFCs.

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