Manganese dioxide cathodes are inexpensive and have high theoretical capacity (based on two electrons) of 617 mAh g−1, making them attractive for low-cost, energy-dense batteries. They are used in non-rechargeable batteries with anodes like zinc. Only ∼10% of the theoretical capacity is currently accessible in rechargeable alkaline systems. Attempts to access the full capacity using additives have been unsuccessful. We report a class of Bi-birnessite (a layered manganese oxide polymorph mixed with bismuth oxide (Bi2O3)) cathodes intercalated with Cu2+ that deliver near-full two-electron capacity reversibly for >6,000 cycles. The key to rechargeability lies in exploiting the redox potentials of Cu to reversibly intercalate into the Bi-birnessite-layered structure during its dissolution and precipitation process for stabilizing and enhancing its charge transfer characteristics. This process holds promise for other applications like catalysis and intercalation of metal ions into layered structures. A large prismatic rechargeable Zn-birnessite cell delivering ∼140 Wh l−1 is shown.
We compare the near-surface composition and electroactivity of commercial indium tin oxide (ITO) thin films, activated by plasma cleaning or etching with strong haloacids, with ITO films that have been freshly deposited in high vacuum, before and after exposure to the atmosphere or water vapor. Conductive-tip AFM, X-ray photoelectron spectroscopy (XPS), and the electrochemistry of probe molecules in solution were used to compare the relative degrees of electroactivity and the near-surface composition of these materials. Brief etching of commercial ITO samples with concentrated HCl or HI significantly enhances the electrical activity of these oxides as revealed by C-AFM. XPS was used to compare the composition of these activated surfaces, focusing on the intrinsically asymmetric O 1s line shape. Energy-loss processes associated with photoemission from the tin-doped, oxygen-deficient oxides complicate the interpretation of the O 1s spectra. O 1s spectra from the stoichiometric indium oxide lattice are accompanied by higher-binding-energy peaks associated with hydroxylated forms of the oxide (and in some cases carbonaceous impurities) and overlapping photoemission associated with energy-loss processes. Characterization of freshly sputter-deposited indium oxide (IO) and ITO films, transferred under high vacuum to the surface analysis environment, allowed us to differentiate the contributions of tin doping and oxygen-vacancy doping to the O 1s line shape, relative to higher-binding-energy O 1s components associated with hydroxyl species and carbonaceous impurities. Using these approaches, we determined that acid activation and O2 plasma etching create an ITO surface that is still covered with an average of one to two monolayers of hydroxide. Both of these activation treatments lead to significantly higher rates of electron transfer to solution probe molecules, such as dimethyferrocene in acetonitrile. Solution electron-transfer events appear to occur at no more than 4x10(7) electroactive sites per cm2 (each with diameters of ca. 50-200 nm) (i.e., a small fraction of the geometric area of the electrode). Electron-transfer rates correlate with the near-surface tin dopant concentration, suggesting that these electroactive sites arise from near-surface tin enrichment.
Zinc
alkaline anodes command significant share of consumer battery
markets and are a key technology for the emerging grid-scale battery
market. Improved understanding of this electrode is required for long-cycle
deployments at kWh and MWh scale due to strict requirements on performance,
cost, and safety. Here we give a modern literature survey of zinc
alkaline anodes with levelized performance metrics and also present
an experimental assessment of leading formulations. Long-cycle materials
characterization, performance metrics, and failure analysis are reported
for over 25 unique anode formulations with up to 1500 cycles and ∼1.5
years of shelf life per test. Statistical repeatability of these measurements
is made for a baseline design (fewest additives) via 15 duplicates.
Baseline design capacity density is 38 mAh per mL of anode volume,
and lifetime throughput is 72 Ah per mL of anode volume. We then report
identical measurements for anodes with improved material properties
via additives and other perturbations, some of which achieve capacity
density over 192 mAh per mL of anode volume and lifetime throughput
of 190 Ah per mL of anode volume. Novel in operando X-ray microscopy
of a cycling zinc paste anode reveals the formation of a nanoscale
zinc material that cycles electrochemically and replaces the original
anode structure over long-cycle life. Ex situ elemental mapping and
other materials characterization suggest that the key physical processes
are hydrogen evolution reaction (HER), growth of zinc oxide nanoscale
material, concentration deficits of OH– and ZnOH4
2–, and
electrodeposition of Zn growths outside and through separator membranes.
We
report for the first time the creation of 2.45 and 2.8 V aqueous
manganese dioxide (MnO2)|zinc (Zn) batteries without the
use of expensive ion-selective membranes separating the anodes and
cathodes. This new high-voltage aqueous battery (HiVAB) is able to
charge and discharge 20–100% of MnO2’s theoretical
capacity (308 mAh/g) repeatedly for many cycles, thereby establishing
this new MnO2|Zn battery as the forerunner for the possible
replacement of lithium-ion batteries for applications where cost,
safety, and energy density characteristics are considered paramount.
We report here the synthesis, characterization, and thin film formation of a polymerizable octa-substituted phthalocyanine (Pc) with styryl-terminated side chains, CuPc(OCH2CH2OCH2CHdCHPh) 8, 2,3,9,10,16,-17,23,24-octakis(2-cinnamyloxyethoxy) phthalocyaninato copper(II) (1). We compare this Pc with a previously discussed phthalocyanine, also possessing styryl groups at the termini of the side chains, but with one alkoxy group in the side chain removed, CuPc(OCH2CH2CHdCHPh)8 (2) (J. Am. Chem. Soc. 2001, 123, 3595). Both 1 and 2 are related to the octa-substituted phthalocyanine CuPc(OCH2CH2OBz)8, 2,3,9,10,-16,17,23,24-octakis (2-benzyloxyethoxy) phthalocyaninato copper(II) (3), which has been shown to form highly coherent rodlike aggregates in Langmuir-Blodgett (LB) films, with excellent control of rod orientation (
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