Solid polymer electrolytes (SPEs) have gained tremendous attention because they are expected to solve the safety problems caused by liquid electrolytes. However, the low ion-transport capacity, insufficient mechanical strength, and unsatisfying flame-retardant properties greatly limit their further application. Here, we designed a poly(ethylene oxide) (PEO)-based SPE by introducing a calcium alginate (CA) nanofiber membrane obtained by electrospinning as a framework. The abundant C═O and -OH groups in the CA macromolecules not only effectively weakened the coordination environment of lithium ions (Li) but also promoted the dissociation of LiTFSI, assisting in the transfer of Li along PEO polymer chains and providing an effective pathway for Li transfer. The introduction of calcium ions (Ca) during the cross-linking process improved the flame-retardant property of the SPE. The obtained SPE exhibited a high ion conductivity (3.86 × 10 S cm, 30 °C), excellent mechanical strength (2.01 MPa), and a wide electrochemical window (5.32 V). The assembled lithium-symmetric battery could undergo stable lithium plating/stripping for 3000 h at 30 °C. Meanwhile, LiFePO (LFP)/Li all-solid-state lithium metal battery showed excellent cycle stability over 300 cycles with a high discharge capacity (141.2 mAh g) and retention rate (92.5%) at 0.3 and 30 °C.
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http://dx.doi.org/10.1021/acsami.4c22242 | DOI Listing |
Nanomaterials (Basel)
February 2025
Graduate School of Engineering Science, Yokohama National University, Yokohama 240-8501, Japan.
We propose a simple and innovative configuration consisting of a quantum dot and micro-optical resonator that emits single photons with good directionality in a plane parallel to the substrate. In this device, a single quantum dot is placed as a light source between the slits of a triangular split-ring micro-optical resonator (SRR) supported in an optical polymer film with an air-bridge structure. Although most of the previous single photon emitters in solid-state devices emitted photons upward from the substrate, operation simulations confirmed that this configuration realizes lateral light emission in narrow regions above, below, left, and right in the optical polymer film, despite the absence of a light confinement structure such as an optical waveguide.
View Article and Find Full Text PDFJ Biomed Opt
March 2025
Universität zu Lübeck, Institute of Biomedical Optics, Lübeck, Germany.
: Selective cryolipolysis is a widely used aesthetic procedure that cools subcutaneous adipose tissue to temperatures as low as to induce fat cell destruction. However, real-time monitoring techniques are lacking, limiting the ability to optimize safety and efficacy. Traditional imaging methods either fail to provide adequate penetration depth or lack the resolution necessary for visualizing subcutaneous fatty tissue dynamics.
View Article and Find Full Text PDFAAPS PharmSciTech
March 2025
Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Colorectal cancer is the second most common cause of death due to growing incidence. Andrographolide (AGD) induces apoptosis in colorectal cancer cells; however, oral administration of AGD is associated with hindered aqueous solubility (3.29 ± 0.
View Article and Find Full Text PDFAAPS PharmSciTech
March 2025
Department of Pharmaceutics and Drug Delivery, School of Pharmacy, University of Mississippi, University, 38677, MS, U.S.A..
The present study aims to develop and characterize cannabidiol (CBD) solid dispersions using Vacuum Compression Molding (VCM) to enhance the drug solubility and release profile. Solid dispersions of CBD and polymers were processed using VCM at 130 °C for 4 min after a prior physical mixing. Five percent w/w of CBD was used with 5% w/w of poloxamer 188 and 90% w/w of polymeric carrier (Polyethylene Oxide, PEO-N80 or Hydroxypropyl cellulose, HPCEF).
View Article and Find Full Text PDFPharm Res
March 2025
Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, 20 Penn Street, Room 623, HSF2 Building, Baltimore, MD, 21201, USA.
Purpose: There are scarce reports on in vitro-in vivo correlation (IVIVC) model development of immediate-release (IR) formulations, and few investigations of the impacts of formulation and process of spray-dried solid dispersions (SDD)-based tablets on human pharmacokinetics (PK), despite commercial product successes. The goal of this study was to investigate the formulation and process factors that impact bioavailability enhancement of IR itraconazole SDD tablets; and to develop an FDA level A IVIVC that would predict in vivo PK performance from in vitro dissolution testing.
Methods: A direct, differential-equation-based IVIVC model approach was employed, using an oral solution for post-dissolution disposition and Fast-, Medium-, and Slow-release tablets.
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