The electrochemical oxidation of propylene carbonate containing 1.0 tool dm -3 LiC104 was investigated with the aid of in situ Fourier transform infrared spectroscopy. The subtractively normalized interracial Fourier transform infrared spectra were obtained for potentials ranging from 4.0 V vs. Li/Li § to 5.0 V vs. Li/Li § From these spectra it is concluded that propylene carbonate decomposes at more positive potentials than does 4.2 V vs. Li/Li § on an Ni electrode. The decomposition products adsorbed on the electrode surface and then gradually dissolved in the electrolyte. From the spectral change for carbonyl groups, it can be seen that the ring opening reaction of propylene carbonate is included in the decomposition process of propylene carbonate electrolytes. On the other hand, the oxidation of propylene carbonate on A1, Pt, and Au electrodes was not observed in the range of potentials investigated. Thus, the oxidation of propylene carbonate containing 1.0 tool dm -3 LiC104 must depend on the electrode material. When the electrode surfaces were analyzed by x-ray photoelectron spectroscopy, those of the Ni and A1 electrodes were found to be covered with their oxides, but oxides were not observed on the Pt or Au electrodes. It is therefore concluded that Ni oxide probably contributes to the decomposition of propylene carbonate.
is thus seen as having the potential to open up new markets for high efficiency lighting. However, reducing manufacturing costs is critical because most OLED lighting still costs too much for the average consumer. As Reineke points out, the only way that costs are likely to come down significantly is through the use of roll-to-roll fabrication methods. [5] Polymer LECs (PLECs) based on fluorescent conjugated poly mers (FCPs) and ion conductors are among the most promising candidates for future lighting systems. [7][8][9][10][11][12][13] PLECs have simple singlelayer structures, which can be fabricated using roll-to-roll methods, using solutions containing both FCPs and ion conductors. [14][15][16][17][18][19] When an external voltage (V a ) higher than the threshold voltage (V th = E g /e: E g is the bandgap of the FCP and e is the elementary charge) is applied between the electrodes, light is generated as a p-n or p-i-n junction is formed as a result of in situ electrochemical doping. [7][8][9][10]20] PLECs have many other advantages, e.g., they can be fabricated using air-stable electrodes and thicker active layers. [21] So in addition to having simple single-layer structures, their other advantages make PLECs particularly well suited to manufacturing by roll-to-roll methods. In addition, it has been reported that certain low-molecularweight compounds, such as pentacene, carbene, and metal complexes, can be used to enable color tuning and improve efficiency. [11,[22][23][24][25][26][27] Realizing high efficiency organic lighting will require more effective light outcoupling technologies. [28][29][30][31][32][33][34][35][36] This is because in conventional organic light-emitting devices, ≈80% of the emitted light is optically trapped between the ITO and organic layers (ITO/organic modes) and in the glass substrate (substrate modes) and lost, and only around 20% of the emitted light can typically be extracted from the devices. In OLEDs, various approaches to enhancing outcoupling have been studied. [28][29][30][31][32][33][34][35] However, there are issues of wavelength selectivity, non-Lambertian angular emission (i.e., the directional problem), and production cost with regard to application of these techniques. To address these issues, Forrest and co-workers developed highly efficient light extraction technologies using a sub anode grid. [35] We, too, have developed efficient Next-generation, power-efficient organic lighting systems, which ideally would be low-cost and mass-producible, are urgently needed because more than 20% of total electricity use goes to lighting. This study presents polymer light-emitting electrochemical cells (PLECs) made using mass-producible nanoimprinted corrugated substrates, which effectively improve light extraction efficiency. The corrugated substrates are fabricated using roll-to-roll methods, using self-assembled block copolymers on glass and film substrates (glass: 0.45 m × 0.55 m, film: 0.6 m wide). Using the glass-type corrugated substrates, two PLECs based on (poly[2-methoxy...
slow, the bulk and surface concentrations of NH3 are assumed to be approximately equal i.e., C3 = C,.Accordingly, the relative change in Cr as a function of electrode area measured along the axis of the reactor is a function of the apparent heterogeneous rate constant (kapp) and the volume flow rate (Vf, cm3 s1) as given bywhere A,0, is the total electrode area, and C,,,,,, and correspond to the concentration of NH3 at the inlet and outlet, respectively, of the reactor. Equation A-3 can be rearranged to give Eq. 5. ABSTRACTElectrochemical oxidation processes on Ni electrodes in propylene carbonate electrolytes were investigated by using cyclic voltammetry, x-ray photoelectron spectroscopy, and in situ Fourier transform infrared spectroscopy. The results of these analyses suggest that Ni electrodes, electrolyte salts, and solvent are oxidized at a greater anodic potential than 4.2 V vs. Li/Li. When propylene carbonate (PC) electrolyte containing LiAsF,, LiBF4, or LiPF, was used, a large amount of Ni fluorides and oxides formed on the Ni electrodes and became inactive in response to Ni oxidation. The Fourier transform infrared measurement showed that the oxidation of PC in these electrolytes is enhanced by the formation of the above-mentioned Ni compounds in the first scan. On the other hand, inactivation was not observed for PC electrolytes containing LiCF3SO3. Correspondingly, the oxidation of PC in this electrolyte was more suppressed than that in the other three electrolytes. When PC containing LiC1O4 was used as an electrolyte, the formation of Ni oxides was observed as well as the active oxidation of PC. This result indicates that Ni oxides are actively involved in the electrochemical oxidation of PC. Thus, electrochemical oxidation processes on Ni electrodes in various PC electrolytes can be explained by the oxidation of Ni electrodes in association with anion decomposition, which determines a type of products formed on Ni electrodes. InfroductionRechargeable lithium batteries are very attractive ) unless CC License in place (see abstract). ecsdl.org/site/terms_use address. Redistribution subject to ECS terms of use (see 169.233.240.12 Downloaded on 2015-03-09 to IP ) unless CC License in place (see abstract). ecsdl.org/site/terms_use address. Redistribution subject to ECS terms of use (see 169.233.240.12 Downloaded on 2015-03-09 to IP
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.