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The photocatalytic degradation of plastic waste represents a pivotal strategy for mitigating the global plastic pollution and fostering resource-efficient utilization. Herein, a facile impregnation method was used to uniformly load various Ni-substituted polyoxometalates (Ni-POMs) onto CdS nanospheres and thus obtain a series of single-cluster Ni-POM@CdS photocatalysts. During visible-light irradiation for 10 h, the catalyst with the highest synergistic photoredox performance (Ni9@CdS-10) achieved an exceptional extent of polylactic acid degradation and H2 productivity (22.29 mmol·gcat−1) exceeding that of pristine CdS ~ 160-fold. The generation of pyruvate—a versatile and valuable chemical—as a degradation product (19.01 mmol·gcat−1) rendered the process highly economically viable. Systematic control experiments and comprehensive characterization analyses indicate that the photocatalytic degradation of plastic waste by Ni9@CdS-10 proceeds via a charge transfer–mediated mechanism, with the Ni9 clusters acting as electron sponges and efficiently extracting photogenerated electrons from CdS to promote H2 evolution while facilitating hole-dominated plastic oxidation. This work provides valuable insights into the development of plastic waste degradation processes promoted by Ni-POM photocatalysts and establishes a practical strategy for converting plastic waste into fuels and chemicals.

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