Photo-charge regulation of metal-free photocatalyst by carbon dots for efficient and stable hydrogen peroxide production

Solar-driven water splitting for hydrogen peroxide (H2O2) production is a sustainable and ultra-clean method. It is difficult for a single-component photocatalyst to meet all the requirements for efficient and stable photoproduction of H2O2. Meanwhile, for multiple-component catalysts, a huge and urgent challenge is to adjust the photo-charge between the multiple components and interfaces of catalysts. Herein, we report a metal-free photocatalyst CN1.8/ICT/CDs composed of CN1.8, organic small molecules (ICT) and N, S-doped carbon dots (CDs) to produce H2O2 efficiently and stably through a dual-channel process. In this catalyst system, CDs are first reported as the active site of water oxidation reaction (WOR) and ICT as the active site of oxygen reduction reaction (ORR), with greatly improved efficiency of the use of photo-charge, and the poisoning of CN1.8/ICT/CDs by H2O2 was prevented. In situ transient photovoltage measurements (TPV) further revealed the photo-charge regulation function of CDs in this multiple-component metal-free photocatalyst. As a result, the CN1.8/ICT/CDs catalyst exhibits a prominent H2O2 production rate of 2202.81 mu mol h(-1) g(-1) (lambda >= 420 nm), which represents the most efficient H2O2 production rate from a metal-free photocatalyst in air atmosphere without sacrificial agents. This work also provides a valid TPV-based method for a deep understanding of complex photocatalytic systems.

Automated summary

A metal-free photocatalyst CN1.8/ICT/CDs composed of CN1.8, ICT, and CDs was developed for efficient and stable production of H2O2. The CDs were identified as the active site for the water oxidation reaction, while ICT served as the active site for the oxygen reduction reaction. This catalyst exhibited a prominent H2O2 production rate, showcasing the potential of metal-free photocatalysts for sustainable and clean H2O2 production.