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Activated by the Li-O-Li configuration with nonbonding O 2p state (lO), anionic redox reaction (ARR) in Li-rich layered oxides (LLOs) contributes to additional capacity but exhibits significant irreversibility, leading to severe surface oxygen loss. Herein, surface nonbonding oxygen state (SNBOS) is regulated by the integrated surface structure engineering to suppress surface oxygen loss and enhance the reversibility of ARR. On the outermost layer, the conversion of layered structure into a LiLaO layer and spinel phase structure eliminates lO, thereby preventing the activation of ARR and suppressing side reactions between electrolyte and oxidized oxygen ions. Besides, by introducing 5d metal La on the near surface, the energy of lO is decreased corresponding to the increased charge-transfer gap Δ and the d-d coulomb repulsion term U is reduced, making U/2 decrease close to Δ and enhancing ARR reversibility. Furthermore, it is demonstrated that the oxidized oxygen of the modified sample cannot become O gas and escape, but rather exists more in the form of high-valence oxygen dimer anions , reducing the reaction depth of surface ARR and inhibiting oxygen loss. Therefore, the designed material demonstrates outstanding cycling stability and kinetics performance.
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http://dx.doi.org/10.1002/anie.202424079 | DOI Listing |
J Am Chem Soc
September 2025
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) State Key Laboratory of Advanced Chemical Power Sources, College of Chemistry, Nankai University, Tianjin 300071, China.
Developing cost-effective spinel oxide catalysts with both high oxygen evolution reaction (OER) activity and stability is crucial for advancing sustainable clean energy conversion. However, practical applications are often hindered by the activity limitations inherent in the adsorbate evolution mechanism (AEM) and the stability limitations associated with the lattice oxygen mechanism (LOM). Herein, we demonstrate structural changes induced by phase transformation in CoMn spinel oxides, which yield more active octahedral sites with shortened intersite distance.
View Article and Find Full Text PDFJCI Insight
September 2025
Division of Cardiovascular Medicine, Department of Medicine.
Aortic valve stenosis is a progressive and increasingly prevalent disease in older adults, with no approved pharmacologic therapies to prevent or slow its progression. Although genetic risk factors have been identified, the contribution of epigenetic regulation remains poorly understood. Here, we demonstrated that histone deacetylase 3 (HDAC3) maintains aortic valve structure by suppressing mitochondrial biogenesis and preserving extracellular matrix integrity in valvular interstitial fibroblasts.
View Article and Find Full Text PDFJTCVS Open
August 2025
Department of Cardiothoracic Surgery, University of Louisville and Norton Children's Hospital, Louisville, Ky.
Objectives: Severe obesity is an established risk factor for adverse cardiovascular events and heart transplantation (HT) outcomes in adults. However, the effect of severe obesity on children after HT is not well studied. We aimed to examine the prevalence and effect of severe obesity on pediatric HT.
View Article and Find Full Text PDFArch Esp Urol
August 2025
Urology Department, Hospital and University Complex of Albacete, 02006 Albacete, Spain.
Background: Delayed graft function is a common situation that leads to increased long-term rates of graft rejection and loss. It is seen increasingly more often, as the use of kidneys from donors after controlled cardiac death has become more widespread. This study aimed to identify factors contributing to its onset and determine how these factors may influence graft survival.
View Article and Find Full Text PDFBMC Res Notes
September 2025
Center for Molecular Medicine Cologne, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.
Objectives: Small cell lung cancer (SCLC) accounts for approximately 15% of lung tumors and is marked by aggressive growth and early metastatic spread. In this study, we used two SCLC mouse models with differing tumor mutation burdens (TMB). To investigate tumor composition, spatial architecture, and interactions with the surrounding microenvironment, we acquired multiplexed images of mouse lung tumors using imaging mass cytometry (IMC).
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