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        <identifier>oai:ynu.repo.nii.ac.jp:02001448</identifier>
        <datestamp>2025-04-30T06:09:00Z</datestamp>
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          <dc:title>Highly porous boron nitride as a metal-free heterogeneous catalyst for cycloaddition of CO2 to epoxides</dc:title>
          <dc:creator>Miyamoto, Teppei</dc:creator>
          <dc:creator>Takagaki, Atsushi</dc:creator>
          <dc:creator>0000-0002-7829-3451</dc:creator>
          <dc:creator>30456157</dc:creator>
          <dc:creator>Song, Jun, Tae</dc:creator>
          <dc:creator>0000-0003-1047-6152</dc:creator>
          <dc:creator>Watanabe, Motonori</dc:creator>
          <dc:creator>0000-0003-3621-4361</dc:creator>
          <dc:creator>Ishihara, Tatsumi</dc:creator>
          <dc:creator>80184555</dc:creator>
          <dc:description>Self-repairing catalysts are useful for achieving alkaline water electrolyzers with long lifetimes under intermittent operation. However, rational methodologies for designing self-repairing catalysts have not yet been established. Herein, hybrid cobalt hydroxide nanosheets (Co-ns), with a high deposition (repairing) rate, and β-FeOOH nanorods (Fe-nr), with high oxygen evolution reaction (OER) ability, are electrostatically self-assembled into composite catalysts. This strategy is developed to integrate multifunctionality in self-repairing catalysts. Positively charged Co-ns and negatively charged Fe-nr form uniform composites when dispersed in an electrolyte. These composites are electrochemically deposited on a nickel electrode by electrolysis at 800 mA cm−2. Co-ns form a conductive mesoporous assembly of CoOOH nanosheets as a support. Fe-nr are then distributed on the CoOOH nanosheets as active sites for the OER. Because of the high deposition rate of Co-ns, the amount of Fe-nr deposited increases 22 times compared to when Fe-nr is deposited alone, and the OER current density increases 14 times compared to that of Co-ns alone. The composite self-repair catalyst shows the highest activity and durability under an accelerated durability test (ADT), and its degradation rate decreases from 84 μV cycle−1 (Fe-nr only) to 60 μV cycle−1 (composite catalyst) under ADT conditions without repair.</dc:description>
          <dc:description>journal article</dc:description>
          <dc:publisher>Royal Society of Chemistry</dc:publisher>
          <dc:date>2024-12-07</dc:date>
          <dc:type>AM</dc:type>
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          <dc:format>application/pdf</dc:format>
          <dc:identifier>Catalysis Science &amp; Technology</dc:identifier>
          <dc:identifier>23</dc:identifier>
          <dc:identifier>14</dc:identifier>
          <dc:identifier>6782</dc:identifier>
          <dc:identifier>6789</dc:identifier>
          <dc:identifier>20444753</dc:identifier>
          <dc:identifier>https://ynu.repo.nii.ac.jp/record/2001448/files/revised_manuscript.pdf</dc:identifier>
          <dc:identifier>https://ynu.repo.nii.ac.jp/record/2001448/files/d4cy01080a1.pdf</dc:identifier>
          <dc:identifier>http://hdl.handle.net/10131/0002001448</dc:identifier>
          <dc:identifier>https://ynu.repo.nii.ac.jp/records/2001448</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:relation>https://doi.org/10.1039/D4CY01080A</dc:relation>
          <dc:rights>embargoed access</dc:rights>
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