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          <dc:title xml:lang="en">Highly porous boron nitride as a metal-free heterogeneous catalyst for cycloaddition of CO2 to epoxides</dc:title>
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            <jpcoar:creatorName xml:lang="en">Miyamoto, Teppei</jpcoar:creatorName>
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              <jpcoar:affiliationName xml:lang="en">Department of Applied Chemistry, Faculty of Engineering, Kyushu University</jpcoar:affiliationName>
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            <jpcoar:creatorName xml:lang="en">Takagaki, Atsushi</jpcoar:creatorName>
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            <jpcoar:creatorName xml:lang="en">Song, Jun, Tae</jpcoar:creatorName>
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              <jpcoar:affiliationName xml:lang="en">Department of Applied Chemistry, Faculty of Engineering, Kyushu University</jpcoar:affiliationName>
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              <jpcoar:affiliationName xml:lang="en">International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University</jpcoar:affiliationName>
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            <jpcoar:creatorName xml:lang="en">Watanabe, Motonori</jpcoar:creatorName>
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              <jpcoar:affiliationName xml:lang="en">Department of Applied Chemistry, Faculty of Engineering, Kyushu University</jpcoar:affiliationName>
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              <jpcoar:affiliationName xml:lang="en">International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University</jpcoar:affiliationName>
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            <jpcoar:creatorName xml:lang="en">Ishihara, Tatsumi</jpcoar:creatorName>
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              <jpcoar:affiliationName xml:lang="en">Department of Applied Chemistry, Faculty of Engineering, Kyushu University</jpcoar:affiliationName>
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              <jpcoar:affiliationName xml:lang="en">International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University</jpcoar:affiliationName>
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          <datacite:description xml:lang="en" descriptionType="Abstract">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.</datacite:description>
          <dc:publisher>Royal Society of Chemistry</dc:publisher>
          <datacite:date dateType="Issued">2024-12-07</datacite:date>
          <dc:language>eng</dc:language>
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          <jpcoar:sourceTitle xml:lang="en">Catalysis Science &amp; Technology</jpcoar:sourceTitle>
          <jpcoar:volume>14</jpcoar:volume>
          <jpcoar:issue>23</jpcoar:issue>
          <jpcoar:numPages>8</jpcoar:numPages>
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