2,522 research outputs found
How Voltage Drops are Manifested by Lithium Ion Configurations at Interfaces and in Thin Films on Battery Electrodes
Battery electrode surfaces are generally coated with electronically
insulating solid films of thickness 1-50 nm. Both electrons and Li+ can move at
the electrode-surface film interface in response to the voltage, which adds
complexity to the "electric double layer" (EDL). We apply Density Functional
Theory (DFT) to investigate how the applied voltage is manifested as changes in
the EDL at atomic lengthscales, including charge separation and interfacial
dipole moments. Illustrating examples include Li(3)PO(4), Li(2)CO(3), and
Li(x)Mn(2)O(4) thin-films on Au(111) surfaces under ultrahigh vacuum
conditions. Adsorbed organic solvent molecules can strongly reduce voltages
predicted in vacuum. We propose that manipulating surface dipoles, seldom
discussed in battery studies, may be a viable strategy to improve electrode
passivation. We also distinguish the computed potential governing electrons,
which is the actual or instantaneous voltage, and the "lithium cohesive energy"
based voltage governing Li content widely reported in DFT calculations, which
is a slower-responding self-consistency criterion at interfaces. This
distinction is critical for a comprehensive description of electrochemical
activities on electrode surfaces, including Li+ insertion dynamics, parasitic
electrolyte decomposition, and electrodeposition at overpotentials.Comment: 35 pages. 10 figure
Water-Splitting Photoelectrolysis Reaction Rate via Microscopic Imaging of Evolved Oxygen Bubbles
Bubble formation and growth on a water-splitting semiconductor photoelectrode under illumination with above-bandgap radiation provide a direct measurement of the gas-evolving reaction rate. Optical microscopy was used to record the bubble growth on single-crystal strontium titanate immersed in basic aqueous electrolyte and illuminated with UV light at 351/364 nm from a focused argon laser. By analyzing the bubble size as a function of time, the water-splitting reaction rate was determined for varying light intensities and was compared to photocurrent measurements. Bubble nucleation was explored on an illuminated flat surface, as well as the subsequent light scattering and electrode shielding due to the bubble. This technique allows a quantitative examination of the actual gas evolution rate during photoelectrochemical water splitting, independent of current measurements
Hearing impairment in Stickler syndrome: a systematic review
BACKGROUND: Stickler syndrome is a connective tissue disorder characterized by ocular, skeletal, orofacial and auditory defects. It is caused by mutations in different collagen genes, namely COL2A1, COL11A1 and COL11A2 (autosomal dominant inheritance), and COL9A1 and COL9A2 (autosomal recessive inheritance). The auditory phenotype in Stickler syndrome is inconsistently reported. Therefore we performed a systematic review of the literature to give an up-to-date overview of hearing loss in Stickler syndrome, and correlated it with the genotype.
METHODS: English-language literature was reviewed through searches of PubMed and Web of Science, in order to find relevant articles describing auditory features in Stickler patients, along with genotype. Prevalences of hearing loss are calculated and correlated with the different affected genes and type of mutation.
RESULTS: 313 patients (102 families) individually described in 46 articles were included. Hearing loss was found in 62.9%, mostly mild to moderate when reported. Hearing impairment was predominantly sensorineural (67.8%). Conductive (14.1%) and mixed (18.1%) hearing loss was primarily found in young patients or patients with a palatal defect. Overall, mutations in COL11A1 (82.5%) and COL11A2 (94.1%) seem to be more frequently associated with hearing impairment than mutations in COL2A1 (52.2%).
CONCLUSIONS: Hearing impairment in patients with Stickler syndrome is common. Sensorineural hearing loss predominates, but also conductive hearing loss, especially in children and patients with a palatal defect, may occur. The distinct disease-causing collagen genes are associated with a different prevalence of hearing impairment, but still large phenotypic variation exists. Regular auditory follow-up is strongly advised, particularly because many Stickler patients are visually impaired
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