Promoting Piezocatalytic H2O2 Production in Pure Water by Loading Metal‐Organic Cage‐Modified Gold Nanoparticles on Graphitic Carbon Nitride

Author:

Fu Meng1,Luo Jinghong1,Shi Bo1,Tu Shuchen2,Wang Zihao3,Yu Changlin3,Ma Zequn4,Chen Xingyuan5,Li Xiangming1ORCID

Affiliation:

1. School of Materials Sciences and Technology Guangdong University of Petrochemical Technology Maoming 525000 China

2. SCNU Environmental Research Institute Guangdong Provincial Key Laboratory of Chemical Pollution and Environmental Safety & MOE Key Laboratory of Theoretical Chemistry of Environment School of Environment South China Normal University Guangzhou 510006 China

3. School of Chemical Engineering Guangdong University of Petrochemical Technology Maoming 525000 China

4. Institute of Materials Science and Devices School of Materials Science and Engineering Suzhou University of Science and Technology Suzhou 215009 China

5. School of Science Guangdong University of Petrochemical Technology Maoming 525000 China

Abstract

AbstractPiezocatalytic hydrogen peroxide (H2O2) production is a green synthesis method, but the rapid complexation of charge carriers in piezocatalysts and the difficulty of adsorbing substrates limit its performance. Here, metal‐organic cage‐coated gold nanoparticles are anchored on graphitic carbon nitride (MOC‐AuNP/g‐C3N4) via hydrogen bond to serve as the multifunctional sites for efficient H2O2 production. Experiments and theoretical calculations prove that MOC‐AuNP/g‐C3N4 simultaneously optimize three key parts of piezocatalytic H2O2 production: i) the MOC component enhances substrate (O2) and product (H2O2) adsorption via host–guest interaction and hinders the rapid decomposition of H2O2 on MOC‐AuNP/g‐C3N4, ii) the AuNP component affords a strong interfacial electric field that significantly promotes the migration of electrons from g‐C3N4 for O2 reduction reaction (ORR), iii) holes are used for H2O oxidation reaction (WOR) to produce O2 and H+ to further promote ORR. Thus, MOC‐AuNP/g‐C3N4 can be used as an efficient piezocatalyst to generate H2O2 at rates up to 120.21 μmol g−1 h−1 in air and pure water without using sacrificial agents. This work proposes a new strategy for efficient piezocatalytic H2O2 synthesis by constructing multiple active sites in semiconductor catalysts via hydrogen bonding, by enhancing substrate adsorption, rapid separation of electron‐hole pairs and preventing rapid decomposition of H2O2.

Publisher

Wiley

Subject

General Chemistry,Catalysis

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