CuO/Cu(OH)2@g-C3N4 derived from CuBTC/g-C3N4 for two channel photocatalytic hydrogen peroxide production
Photocatalytic production of H 2 O 2 is indeed a safe, sustainable and cost-effective technology, offering an environmentally friendly solution to the energy crisis through solar photocatalysis. However, it still faces challenges such as reliance on organic electron donors and pure O 2 , as well as inefficiencies in hole utilization. To overcome these limitations, a dual-channel photocatalytic system has been developed. In this study, we showcase the efficiency of the CuO/Cu(OH) 2 @g-C 3 N 4 composite, derived from CuBTC/g-C 3 N 4 via NaOH treatment, as a high-performance dual-channel photocatalyst for H 2 O 2 production. Under visible light (λ ≥ 420 nm), this composite achieves a H 2 O 2 yield of 1354 μmol/L in 120 min without any sacrificial agent, outperforming g-C 3 N 4 by 8.4 times, CuO by 13.6 times and CuO@g-C 3 N 4 by 1.9 times. Quenching experiments and electron paramagnetic resonance spectra confirmed that HO • and O 2 •− are intermediate products in the photocatalytic process, following a two-step single-electron reaction pathway. The superior activity of CuO/Cu(OH) 2 @g-C 3 N 4 in H 2 O 2 generation can be attributed to the synergistic effects of OH bonds on the CuO@g-C 3 N 4 Z-type heterojunction and Cu(OH) 2 . This research presents a straightforward and promising approach for developing highly efficient photocatalysts for energy conversion.
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