The use of ordered catalyst layers, based on micro-/nanostructured arrays such as the ordered Nafion array, has demonstrated great potential in reducing catalyst loading and improving fuel cell performance. However, the size (diameter) of the basic unit of the most existing ordered Nafion arrays, such as Nafion pillar or cone, is typically limited to micron or submicron sizes. Such small sizes only provide a limited number of proton transfer channels and a small specific area for catalyst loading. In this work, the ordered Nafion array with a pillar diameter of only 40 nm (D40) was successfully prepared through optimization of the Nafion solvent, thermal annealing temperature, and stripping mode from the anode alumina oxide (AAO) template. The density of D40 is 2.7 × 10 pillars/cm, providing an abundance of proton transfer channels. Additionally, D40 has a specific area of up to 51.5 cm/cm, which offers a large area for catalyst loading. This, in turn, results in the interface between the catalyst layer and gas diffusion layer becoming closer. Consequently, the peak power densities of the fuel cells are 1.47 (array as anode) and 1.29 W/cm (array as cathode), which are 3.3 and 2.9 times of that without array, respectively. The catalyst loading is significantly reduced to 17.6 (array as anode) and 61.0 μg/cm (array as cathode). Thus, the nanosized Nafion array has been proven to have high fuel cell performance with low Pt catalyst loading. Moreover, this study also provides guidance for the design of a catalyst layer for water electrolysis and electrosynthesis.
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http://dx.doi.org/10.1021/acsnano.3c01690 | DOI Listing |
Nature
January 2025
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, USA.
Crosslinked thermosets are highly durable materials, but overcoming their petrochemical origins and inability to be recycled poses a grand challenge. Many strategies to access crosslinked polymers that are bioderived or degradable-by-design have been proposed, but they require several resource-intensive synthesis and purification steps and are not yet feasible alternatives to conventional consumer materials. Here we present a modular, one-pot synthesis of degradable thermosets from the commercially available, biosourced monomer 2,3-dihydrofuran (DHF).
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
In this study, we synthesized CeO possessing an open pore structure and verified its structural differences compared to CeO lacking such an open pore structure. Using these two CeO samples as catalyst supports and loading them with Pd metals, a series of characterizations were carried out on the resultant catalysts to analyze their structures and properties meticulously. We have elucidated the influence of the open pore structure on the loading position of Pd.
View Article and Find Full Text PDFChemSusChem
January 2025
Peking University, Chemistry, 292 Chengfu Rd, 100871, Beijing, CHINA.
Polyesters featuring a linear topology and in-chain 1,3-cyclobutane rings, synthesized via ring-opening polymerization (ROP) of 2-oxabicyclo[2.1.1]hexan-3-one (4R-BL, R = Bu, Ph) through a coordination-insertion mechanism, display excellent thermal and hydrolytic stability, making them promising candidates for sustainable circular materials.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Chang Chun Institute of Applied Chemistry Chinese Academy of Sciences, Key Laboratory of Polymer Ecomaterials, 5625 Renmin Street, Changchun, , 130022, Changchun, CHINA.
Living cationic polymerization (LCP) is a classical technique for precision polymer synthesis; however, due to the high sensitivity of cationic active species towards chain-transfer/termination events, it is notoriously difficult to control polymerization under mild conditions, which inhibits its progress in advanced materials engineering. Here, we unlock a practical anion-binding catalytic strategy to address the historical dilemma in LCP. Our experimental and mechanistic studies demonstrate that commercially accessible hexafluoroisopropanol (HFIP), when used in high loading, can create higher-order HFIP aggregates to tame dormant-active species equilibrium via non-covalent anion-binding principle, in turn inducing distinctive polymerization kinetics behaviors that grant efficient chain propagation while minimizing competitive side reactions.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Chemical and Environmental Engineering, Yale University, New Haven, CT, USA.
Discharge of wastewater containing nitrate (NO) disrupts aquatic ecosystems even at low concentrations. However, selective and rapid reduction of NO at low concentration to dinitrogen (N) is technically challenging. Here, we present an electrified membrane (EM) loaded with Sn pair-atom catalysts for highly efficient NO reduction to N in a single-pass electrofiltration.
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