期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 11, 期 11, 页码 5925-5936出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ta00196b
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By introducing Rb+ ions, the PCN photocatalyst was modified to have more edge active sites and improved hydrophilicity and O2 adsorption capacity, leading to a higher H2O2 yield. Experimental and theoretical results showed that CNR-0.5 followed a two-step single-electron O2 reduction reaction pathway in the H2O2 photogeneration reaction. CNR-0.5 exhibited excellent photocatalytic H2O2 production performance in a real water body, expanding the practical applications of PCN materials.
The H2O2 yield is substantially hindered by the four-electron competitive reaction and limited oxygen-capture ability of PCN. We herein demonstrated a Rb+-modified PCN photocatalyst (CNR-0.5) for highly efficient H2O2 production, in which the introduction of Rb+ ions creates abundant edge active sites within the-C equivalent to N/-OH groups of the triazine ring. The hydrophilicity and O-2 adsorption capacity of the PCN catalyst were significantly improved. As a result, CNR-0.5 achieved a relatively high H2O2 yield (2225.05 mmol g(-1) h(-1)), which is 37.58 times higher than that of pristine PCN under white light-emitting diode (LED) light. Experimental and theoretical results demonstrated that CNR-0.5 followed a two-step single-electron O2 reduction reaction pathway in the H2O2 photogeneration reaction. Additionally, the AQE of CNR-0.5 was 24.52% at 385 nm in an ethanol system with O-2 injection. The excellent photocatalytic H2O2 production performance of CNR-0.5 in a real water body broadens the path for practical applications of PCN materials in photocatalytic H2O2 production.
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