Publications by authors named "Y Iwasawa"

On-purpose atomic scale design of catalytic sites, specifically active and selective at low temperature for a target reaction, is a key challenge. Here, we report teamed Pd and Mo single-atom sites that exhibit high activity and selectivity for anisole hydrodeoxygenation to benzene at low temperatures, 100-150 °C, where a Pd metal nanoparticle catalyst or a MoO nanoparticle catalyst is individually inactive. The catalysts built from Pd or Mo single-atom sites alone are much less effective, although the catalyst with Pd sites shows some activity but low selectivity.

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  • Heart Failure (HF) is a prevalent and costly chronic condition with high rates of hospitalization and a need for effective disease management, particularly through self-care interventions for outpatients.
  • This study aims to compare a structured nurse-led support intervention for chronic HF patients to usual medical care, focusing on self-care behaviors and rehospitalization rates.
  • The trial will involve 40 facilities and 210 adult participants diagnosed with chronic HF, assessing the effectiveness of structured nursing support through regular follow-ups on improving self-care and reducing hospital readmissions.
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Highly efficient, cost-effective, and durable electrocatalysts, capable of accelerating sluggish reaction kinetics and attaining high performance, are essential for developing sustainable energy technologies but remain a great challenge. Here, we leverage a facile heterostructure design strategy to construct atomically thin Os@Pd metallenes, with atomic-scale Os nanoclusters of varying geometries confined on the surface layer of the Pd lattice, which exhibit excellent bifunctional properties for catalyzing both hydrogen evolution (HER) and oxygen reduction reactions (ORR). Importantly, Os@Pd metallenes manifest a low η overpotential of only 11 mV in 1.

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We aimed to investigate the reliability and validity of sweat lactate threshold (sLT) measurement based on the real-time monitoring of the transition in sweat lactate levels (sLA) under hypoxic exercise. In this cross-sectional study, 20 healthy participants who underwent exercise tests using respiratory gas analysis under hypoxia (fraction of inspired oxygen [FiO], 15.4 ± 0.

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  • The study explores how disruptions in the glutathione-based lipid redox system cause increased oxidized lipid production and cell death (ferroptosis) during ischemia-reperfusion (IR) events in cardiomyocytes.
  • Clinical methods such as microdialysis and high-resolution mass spectrometry were used to analyze metabolite fluctuations, revealing significant glutathione release into extracellular spaces and decreased intracellular levels during IR.
  • The research also showed that inhibiting the transporter MRP1 can reduce reactive oxygen species and lipid peroxidation, thus preventing ferroptosis and potential cell death following ischemic events.
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