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    <identifier>10.57760/sciencedb.08241</identifier>
    <datestamp>2024-06-17T10:19:13Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2024-06-17</dc:date>
  <dc:title>Efficient hydrogen peroxide photogeneration over GaOOH/In(OH)3 composites via the half-reaction of tetracycline oxidation</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.08241</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Material Characterization: The phase state and crystal structure of GaOOH/In(OH)3 composites were observed by X-ray diffraction (XRD, PANalytical X&amp;rsquo; pert powder). The morphology and size of obtained samples were imaged by scanning electron microscopy (SEM, Hitachi SU8000), transmission electron microscopy (TEM, JEOL JEM-F200). The specific surface area of samples was observed by nitrogen adsorption with a TriStar II Plus 3.03 instrument. UV&amp;ndash;vis diffuse reflectance spectra and photoluminescence (PL) spectra were recorded by a UV 3600 UV&amp;ndash;vis spectrometer and a FLS1000 transient steady-state fluorescence spectrometer respectively.&amp;nbsp;Electron spin resonance (ESR) spectra were obtained by a Bruker model A300-10/12 with TEMPO as spin trapping agent. The elemental composition of samples was analyzed by X-ray photoelectron spectroscopy (XPS, Thermo escalab 250XI). EIS electrochemistry workstation (CHI760E, Shanghia Zhenhua Tech. Co., Ltd., China) at room temperature. 20 mg powder sample was dispersed into 500 &amp;mu;L Nafion and 500 &amp;mu;L of water under ultrasonication for 30 min. The as-prepared samples coated on an ITO glass acted as the working electrode with an active area of 1 cm2, whereas a Pt wire and calomel electrode were used as the counter and reference electrode respectively. 50 mL 0.5 M Na2SO4 aqueous solution was selected as the electrolyte.Computational details: Density functional theory (DFT) calculations were using the Cambridge Serial Total Energy Package (CASTEP) module. Generalized gradient approximation (GGA) with the Perdew-Burke Ernzerhof (PBE) function was selected to study the exchange-correlation interaction. The sampling of the Brillouin zone was conducted using a 3 &amp;times; 4 &amp;times; 1 k-point grid for GaOOH. The sampling of the Brillouin zone was conducted using a 2 &amp;times; 2 &amp;times; 1 k-point grid for In(OOH)3.and The sampling of the Brillouin zone was conducted using a 1 &amp;times; 2 &amp;times; 1 k-point grid for GaOOH/In(OOH)3. To assure rigorous consistency, calculations were performed until the energy convergence threshold was less than 10-5 eV. To effectively isolate periodic structures and preclude their interaction, a vacuum buffer of 15 &amp;Aring; was inserted along the z-axis. The unit cell of GaOOH is defined by the lattice constants: a = 9.77900 &amp;Aring;, b = 5.93200 &amp;Aring;, and c = 22.23640 &amp;Aring;. &amp;alpha;=&amp;beta;=&amp;gamma;= 90&amp;deg;; The unit cell of In(OOH)3 is defined by the lattice constants: a = 15.94860 &amp;Aring;, b = 11.27740 &amp;Aring;, and c = 23.51440 &amp;Aring;. &amp;alpha;=&amp;beta;=&amp;gamma;= 90&amp;deg;; The unit cell of In(OOH)3 is defined by the lattice constants: a = 18.00000 &amp;Aring;, b = 11.57070 &amp;Aring;, and c = 25.14290 &amp;Aring;. &amp;alpha;=&amp;beta;=&amp;gamma;= 90&amp;deg;.Section 3:	The DPD-POD colorimetric method was used to measure the H2O2 content. N,N-diethyl-phenylenediamine and horseradish peroxidase were the chromogenic agents respectively, and the buffer was 0.1M phosphate solution.Preparation of chromogenic agents: 0.1 g DPD dissolved in 10 mL 0.1 M H2SO4 solution to obtain 10 mg mL-1 DPD solution. 0.01 g POD dissolved in 10 mL deionized water to obtain 1mg mL-1 POD solution. Store both solutions at 4℃ for one week.Preparation of phosphate solution: 99.7 mL deionized water, 87.7 mL 1M sodium dihydrogen phosphate solution, 12.6 mL disodium hydrogen phosphate solution mixed.Detection procedures: The 1 mL sample was added with 0.4 mL phosphate buffer, 1.12 mL deionized water, 50 &amp;mu;L DPD solution and 50 &amp;mu;L POD solution, mixed evenly and poured into a colorimetric dish. The absorbance of the solution was measured at 551 nm wavelength. Since the DPD solution is easily oxidized, the detection process is completed within 6 minutes after adding the chromogenic agents.</dc:description>
  <dc:subject>H2O2 photogeneration; GaOOH/In(OH)3 Type II heterojunctions; Tetracycline oxidation half-reaction; Hole consumption; Enhanced electron formation</dc:subject>
  <dc:creator>Ting Yu</dc:creator>
  <dc:creator>Ying Liang</dc:creator>
  <dc:creator>Zejun Zhou</dc:creator>
  <dc:creator>Fengjie Chen</dc:creator>
  <dc:creator>Yingjun Wang</dc:creator>
  <dc:creator>Yunjun Mei</dc:creator>
  <dc:creator>Mengxi Cao</dc:creator>
  <dc:creator>Bolei Chen</dc:creator>
  <dc:creator>Pu Wang</dc:creator>
  <dc:creator>Yawei Wang</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:publisher>Science Data Bank</dc:publisher>
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