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Semiconductor photocatalysis is a potential solution to meet energy needs with green and inexhaustible solar energy. However, designing efficient and stable photocatalysts is a challenging task due to the limited ability to effectively separate electrons and holes. In this paper, by using a straightforward ethanol dispersion technique, we were able to combine ultrathin layered Cu-TCPP MOFs with g-C3N4 nanosheets, resulting in the creation of an extremely effective nano-composite photocatalyst with exceptional UV-vis activity. CT/CN heterojunctions displayed remarkable photocatalytic efficacy for the production of H2, with 3CT/CN showcasing a five-fold enhancement in photoactivity as compared to the unadorned g-C3N4. Based on the results of photoluminescence spectroscopy, electrochemical impedance spectroscopy, and electrochemical reduction, the considerably improved charge transfer and separation, together with the possible catalytic capability of uniformly distributed metal nodes in Cu-TCPP, are believed to be the underlying reason for the observed exceptional photoactivity. After thorough analysis, a potential process for charge transfer and segregation between g-C3N4 and Cu-TCPP has been suggested. [ABSTRACT FROM AUTHOR]

Catalysts with low cost, high efficiency, and no need for precious metal cocatalysts are the key to realizing the maximum utilization of solar energy-efficient hydrogen (H2) production. In this study, a series of graphitic carbon nitride-derived catalysts (g-C3N4/CoP@C) were successfully obtained by in situ phosphating of g-C3N4/Co-BDC. A CoP@C cocatalyst developed with Co-BDC nanosheets as precursors can accelerate the H2 generation of g-C3N4. The close interface between CoP@C and g-C3N4 increased the electron–hole separation efficiency. Moreover, the CoP@C surface carbon accelerated electron transfer and increased the light absorption range. The prepared g-C3N4/CoP@C composite material exhibited H2 production capability up to 1968 μmol g−1 (3 h), approximately 129.9 times that of g-C3N4. Therefore, the CoP@C cocatalyst is proposed as an alternative to non-precious metal cocatalysts based on the findings of the study. [ABSTRACT FROM AUTHOR]