The generation of hydrogen through photocatalysis is a fascinating technology for addressing environmental concerns and the energy crisis. Nevertheless, the quest for cost-effective, stable, and efficient photocatalysts in the realm of energy conversion remains a significant challenge. Herein, we designed novel InVO 4 /Ti 3 C 2 MXene (IVTC) heterostructures by employing acid etching to produce Ti 3 C 2 MXene with an accordion-like morphology, using the hydrothermal technique for the production of orthorhombic InVO 4 nanoparticles (NPs), and integrating them through a self-assembly approach. Both field-emission scanning electron microscopy and HRTEM analyses revealed a consistent distribution of InVO 4 NPs with an average size of 43.4 nm on both surfaces and between the sheets of Ti 3 C 2 MXene. The intimate interface between the Ti 3 C 2 MXene nanosheet and InVO 4 suppressed carrier recombination and promoted charge transfer, thereby boosting photocatalytic H 2 production. Under visible light exposure, the rate of hydrogen evolution is enhanced in IVTC heterostructures containing an optimized 10% loading of InVO 4 , exhibiting over a 3-fold increase compared to pristine InVO 4 NPs, maintaining efficiency across four cycles. This research presents a promising method for designing and creating high-efficiency heterostructures possessing excellent visible-light-driven photocatalytic activity for H 2 evolution.