Effect of Iodide-Based Organic Salts and Ionic Liquid Additives in Dye-Sensitized Solar Cell Performance.

The use of ionic liquid and organic salts as additives for electrolyte systems in dye-sensitized solar cells have been widely described in recent years. The tunability of their physical-chemical properties according to the cation-anion selection contributes toward their high efficiencies. For this purpose, several iodide-based organic salts including imidazolium, picolinium, guanidinium and alkylammonium cations were tested using acetonitrile/valeronitrile electrolytes and their photovoltaic parameters were compared. A best efficiency of 4.48% (4.15% for the reference) was found for 1-ethyl-2,3-dimethylimidazolium iodide ([C2DMIM]I) containing electrolyte, reaffirming the effectiveness of these additives. 4-tertbutylpyridine was included into the formulation to further improve the performance while determining which iodide salts demonstrate the highest synergy with this additive. [C2DMIM]I once again proved to be the superior additive, achieving an efficiency of 6.48% (6% for the reference). Electrochemical impedance spectroscopy was employed to elucidate the effects of the various additives, demonstrating the relevance of the counter electrode resistance on device performance. Finally, several computational descriptors for the cationic structures were calculated and correlated with the photovoltaic and resistance parameters, showing that properties related to polarity, namely relative positive charge, molecular polarizability and partition coefficient are in good agreement with the counter-electrode resistance.

Development of cellulose-based polymeric structures using dual functional ionic liquids.

Carboxylate ionic liquids (ILs) combining benzethonium (BE) and didecyldimethylammonium (DDA) as cations have been explored to be used for the first time as dual functional solvents for microcrystalline cellulose (MCC) dissolution and, subsequently development of polymeric structures. Considering that some ILs can remain in the polymeric structures after phase inversion, these ILs can offer advantages such as antibacterial/antimicrobial response and ability to disrupt H-bonds. In this context, all tested ILs have been able to dissolve MCC up to a concentration of 4% (w/w), resulting in different polymeric structures, such as gel-like or films, depending on the type of IL and the ratio between MCC and IL. Furthermore, FTIR spectroscopy showed that some IL remains in the polymeric structures, which can enhance their application in the biomedical field.

Tetramethylguanidine-based gels and colloids of cellulose.

Novel and stable gels of cellulose were produced. These gels are prepared at room temperature by combination of cellulose and tetramethylguanidine (TMG) in different ratios (1:1, 1:2, 1:3 in equivalents of alcohol groups of cellulose per number of molecules of TMG). Detailed NMR, SEM, rheological and XRD studies of these gels were carried out. The concentration of cellulose in the gel, temperature, frequency of oscillation and shear rate were used as variables in order to understand the fundamentals and optimize operational conditions, considering their possible use as matrices for CO2 capture. Cellulose recovery from a specific gel was performed using ethanol as precipitating agent, leading to a lower crystallinity, which permits to consider this polymer in further studies associated to physical/chemical modification of cellulose.

Bis(bipyridinium) Salts as Multicolored Electrochromic Devices.

Symmetrical and nonsymmetrical oxobis(bipyridinium) cations combined with iodide and bistriflimide anions were prepared. In the case of the bistriflimide-based bis(bipyridinium) salts, two room-temperature ionic liquids (RTILs) with a combination of linkers and terminal ethers, [(C3 O)bpy(C4 O)bpy(C3 O)][NTf2 ]4 and [(C10 )bpy(C4 O)bpy(C3 O)][NTf2 ]4 , were obtained, with glass transition temperatures (between -6.9 and 6.0 °C) higher than those reported previously for salts of dication bipyridinium scaffolds (-17.5 to -30.0 °C). The prepared salt containing [(C10 )bpy(C4 O)bpy(C10 )][NTf2 ] can form an ionic liquid crystal structure. The most promising salts were tested as efficient and reversible multicolored electrochromic devices through cyclic voltammetry studies and detailed characterizations of their electrochromic performances. In general, tetracations based on oxobis(bipyridinium) salts show higher chromatic contrast and lower coloration efficiency than similar dication salts. Exchange of the anion from iodide to [NTf2 ] increases the transition times and coloration efficiencies for all the prepared di- and tetracation salts. The electrochromic device stability of [(C3 O)bpy(C4 O)bpyC3 O]I4 was tested by on/off cycling; this device loses around 23 % of the initial color after 8640 redox cycles and shows very good cycling stability compared with previously reported diiodide salts.

4'-carboxy-7-hydroxyflavylium. A multistate system involving twelve species reversibly interconverted by pH and light stimuli.

In the frame of the metamorphosis chemistry, where complexity is achieved at the bottom, a multistate system based on 4'-carboxy-7-hydroxyflavylium is described. Twelve species reversibly interconverted by pH and light stimuli were identified at the equilibrium or as transients. The carboxylic substituent deprotonates at moderately acidic pH values and as a consequence allows the existence of two photoactive trans-chalcones, whose irradiation leads to different photoproducts. The thermodynamic and kinetic properties of the network of reactions of the multistate system were investigated by means of UV-vis spectroscopy, stopped-flow, continuous irradiation, and flash photolysis. The evolution of the system to the equilibrium when the pH is raised from acidic to higher pH values can take place through two different routes involving the protonated or the deprotonated species at the carboxylic acid substituent. The kinetics and the photochromism of the system were rationalized by means of an energy level diagram.

Novel bipyridinium ionic liquids as liquid electrochromic devices.

Novel mono and dialkylbipyridinium (viologens) cations combined with iodide, bromide, or bis(trifluoromethanesulfonyl)imide [NTf2] as anions were developed. Selective alkylation synthetic methodologies were optimized in order to obtain the desired salts in moderate to high yields and higher purities. All prepared mono- and dialkylbipyridinium salts were completely characterized by (1)H, (13)C, and (19)F NMR spectroscopy, Fourier-transform IR spectroscopy, and elemental analysis (in the case of NTf2 salts). Melting points, glass transition temperatures by differential scanning calorimetry (DSC) studies, and decomposition temperatures were also checked for different prepared organic salts. Viscosities at specific temperatures and activation energies were determined by rheological studies (including viscosity dependence with temperature in heating and cooling processes). Electrochemical studies based on cyclic voltammetry (CV), differential pulsed voltammetry (DPV), and square-wave voltammetry (SWV) were performed in order to determine the redox potential as well as evaluate reversibility behavior of the novel bipyridinium salts. As proof of concept, we developed a reversible liquid electrochromic device in the form of a U-tube system, the most promising dialkylbipyridinium-NTf2 ionic liquid being used as the electrochromic material and the room-temperature ionic liquid (RTIL), 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)-imide [EMIM][NTf2], as a stable and efficient electrolyte.