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    <identifier>10.57760/sciencedb.23468</identifier>
    <datestamp>2025-04-17T13:45:26Z</datestamp>
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  <dc:date>2025-04-17</dc:date>
  <dc:title>Revealing the dynamics of charge carriers in organic/inorganic hybrid FS-COF/WO3 S-scheme heterojunction for boosted photocatalytic hydrogen evolution</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.23468</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Designing high-efficiency photocatalysts by the construction of organic/inorganic heterojunctions is considered to be an effective approach for improving photocatalytic hydrogen evolution reaction (HER) activity. This work designed and built unique S-scheme heterojunctions by in-situ growing inorganic WO3 nanoparticles with excellent oxidation ability on fused-sulfone-modified covalent organic frameworks (FS-COF) with strong reduction ability. It is found that FS-COF and WO3 have a well-matched staggered band alignment. The best-designed FS-COF/WO3-20% exhibits a maximum photocatalytic HER rate of 24.7 mmol g-1 h-1 under visible light irradiation, which is 1.4 times greater than the pure FS-COF. Moreover, photogenerated electron-hole pairs can be separated and utilized more efficiently thanks to the FS-COF/WO3 heterojunction's ability to create a favorable internal electric field resulting from the difference in work functions between FS-COF and WO3, which speeds up the transfer dynamics of photoinduced electrons from WO3 to FS-COF through an additional interfacial electron-transfer channel obeying the directional S-scheme migration mechanism. Furthermore, the S-scheme migration mechanism of photoinduced charge carriers instead of the type-II mechanism was confirmed by the signal intensity of &amp;bull;O2&amp;minus; species from spin-trapping electron paramagnetic resonance (EPR) spectra over the single component and the formed heterojunction. It ensures the photoexcited electrons maintain on the lowest unoccupied molecular orbital (LUMO) of FS-COF with a strong reduction ability to participate in photocatalytic HER, resulting in a significantly boosted H2 evolution rate. Based on organic/inorganic coupling, this work offers a strategy for creating particular S-scheme heterojunction photocatalysts.</dc:description>
  <dc:subject>S-scheme heterojunction; Photocatalytic hydrogen evolution; Covalent organic frameworks; Dynamics of charge carriers; Organic/inorganic hybrid</dc:subject>
  <dc:creator>Yunchao Zhang</dc:creator>
  <dc:creator>Jinkang Pan</dc:creator>
  <dc:creator>Xiang Ni</dc:creator>
  <dc:creator>Feiqi Mo</dc:creator>
  <dc:creator>Yuanguo Xu</dc:creator>
  <dc:creator>Pengyu Dong</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-sa/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/10.1016/s1872-2067(25)64664-x</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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