High cost and poor stability of the oxygen reduction reaction (ORR) electrocatalysts are the major barriers for broad-based application of polymer electrolyte membrane fuel cells. Here we report a facile and scalable approach to improve Pt/C catalysts for ORR, by modification with small amounts of hydrophobic ionic liquid (IL). The ORR performance of these IL-modified catalysts can be readily manipulated by varying the degree of IL filling, leading to a 3.4 times increase in activity. Besides, the IL-modified catalysts exhibit substantially enhanced stability relative to Pt/C. The enhanced performance is attributed to the optimized microenvironment at the interface of Pt and electrolyte, where advantages stemming from an increased number of free sites, higher oxygen concentration in the IL and electrostatic stabilization of the nanoparticles develop fully, at the same time that the drawback of mass transfer limitation remains suppressed. These findings open a new avenue for catalyst optimization for next-generation fuel cells.
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http://dx.doi.org/10.1021/am5074003 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Developing damping materials that are both optically transparent and mechanically robust, while offering broad frequency damping capacity, is a significant challenge─particularly for devices that require protection without compromising visual clarity. Conventional methods often either fail to maintain transparency or involve complex designs that are difficult to implement. Here, we present an ionogel system that integrates a physically cross-linked elastic copolymer network with a viscous ionic liquid.
View Article and Find Full Text PDFRSC Adv
January 2025
Department of Physics, BITS Pilani-Pilani Campus RJ-333031 India
The study reports solid-state ceramic supercapacitors (SSCs) assembled using a novel composite electrolyte based on Li ion conducting perovskite-type LLTO (LiLaTiO) and an ionic liquid (EMIM BF). Small amounts of various ionic liquids (ILs) were added to LLTO to enhance the ionic conductivity and improve electrode compatibility. The optimal composition with approximately ∼6 wt% EMIM BF in LLTO exhibited a high ionic conductivity of around ∼10 Ω cm at room temperature, nearly three orders of magnitude higher than that of the pristine LLTO.
View Article and Find Full Text PDFSmall
January 2025
Department of Chemical Engineering, POSTECH, Pohang, 37673, Republic of Korea.
Liquid crystals (LCs) are widely used as promising stimuli-responsive materials due to their unique combination of liquid and crystalline properties, providing the capability to sense even molecular-scale events and amplify them into macroscopic optical outputs. However, encoding a high level of selectivity to a specific intermolecular event remains a key challenge, leading to prior studies regarding chemically functionalized LC interfaces. Herein, we propose an integrative strategy to significantly advance the design of chemo-responsive LCs through a deep fundamental understanding on the orientational coupling of LCs with new functional molecules, organic ionic plastic crystals (OIs), presented at LC interfaces.
View Article and Find Full Text PDFNat Commun
January 2025
Laboratory for Chemistry and Life Science, Institute of Integrated Research, Institute of Science Tokyo, Yokohama, 226-8501, Japan.
Atomically flat two-dimensional networks of boron are attracting attention as post-graphene materials. An introduction of cations between the boron atomic layers can exhibit unique electronic functions that are not achieved by neutral graphene or its derivatives. In the present study, we propose a synthesis strategy for ion-laminated boron layered materials in a solution phase, which enables the preparation of analogs by changing the alkali-metal species.
View Article and Find Full Text PDFNat Commun
January 2025
Shenzhen Geim Graphene Center, Tsinghua-Berkeley Shenzhen Institute & Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen, P. R. China.
The unsatisfactory ionic conductivity of solid polymer electrolytes hinders their practical use as substitutes for liquid electrolytes to address safety concerns. Although various plasticizers have been introduced to improve lithium-ion conduction kinetics, the lack of microenvironment understanding impedes the rational design of high-performance polymer electrolytes. Here, we design a class of Hofmann complexes that offer continuous two-dimensional lithium-ion conduction channels with functional ligands, creating highly conductive electrolytes.
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