Yifei Liang, Fulai Liu, Fulai Liu, Fan Liu, Fan Liu, Rui Shi, Jing Li, Lei Kang, Yong Chen
ABSTRACT Hydroxymethylsulfonate (HMS) is an important cleaning agent in the electronics industry and serves as a crucial intermediate in the synthesis of surfactants and pharmaceuticals. Conventional industrial production of HMS relies on toxic and volatile formaldehyde, presenting considerable safety and environmental risks. Herein, we report a solar‐driven photocatalytic route for the synthesis of HMS from waste SO 2 and polyethylene terephthalate (PET)‐derived ethylene glycol (EG) under ambient conditions, using a Cu single‐atom‐decorated TiO 2 catalyst (Cu 1 /TiO 2 ). The optimized Cu 1 /TiO 2 catalyst achieves an HMS yield rate of ∼ 2.31 mmol g cat −1 h −1 with a 77.5% carbon selectivity, along with a H 2 evolution rate of ∼ 4.36 mmol g cat −1 h −1 . Mechanistic studies reveal that the atomically dispersed Cu sites act as electron sinks, which enhance charge separation and induce electronic modulation of TiO 2 . This modulation facilitates the adsorption and activation of reactants while lowering the energy barrier for the formation of a key *CHOH─CH 2 OH intermediate via EG dehydrogenation. This resulting intermediate then undergoes nucleophilic attack by hole‐generated •SO 3 − , triggering C─C cleavage to form HMS. This work establishes a sustainable and waste‐valorizing route for organosulfur synthesis.