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Laser-Anchored Ru Single-Atoms Enable Paired PET Plastic and Nitrate Upcycling into Formate and Ammonia

ACS Catalysis 2026
Jangyun Kim, Jayaraman Theerthagiri, Juhyeon Park, Piyapa Junmon, Nuttapon Yodsin, Myong Yong Choi

Summary

Scientists developed a fast, laser-based method to create a specialized catalyst that can simultaneously break down two harmful pollutants — nitrate (a common water contaminant from fertilizer runoff) and PET plastic waste — turning them into useful products like ammonia and formate. This matters because it offers a potential way to clean up nitrate-contaminated water and recycle plastic waste at the same time, rather than treating them as separate problems, though this is still early-stage lab research using electricity-driven chemistry rather than a ready-to-use consumer solution.

Polymers

Electrochemical upcycling of nitrate (NO 3 − ) and polyethylene terephthalate (PET) waste into value-added chemicals offers a promising strategy for simultaneous pollution mitigation and resource recovery. However, progress in this field is hindered by the limited availability of high-performance electrocatalysts. Herein, we report a rapid CO 2 laser irradiation strategy for synthesizing Ru single-atom (RuSA) catalysts anchored on L-tryptophan (Trp) nanodomain-assembled Co 3 O 4 nanocubes (RuSA/Trp-Co 3 O 4 ) within 3 min, enabling high active-site exposure and utilization efficiency for both the electrocatalytic nitrate reduction reaction (NO 3 RR) and the ethylene glycol oxidation reaction (EGOR), where ethylene glycol (EG) is a key PET-derived monomer. The electron-rich Ru−N and Ru−O coordination environments, together with strong metal−support interactions, modulate the electronic structure, inducing a downward shift of the d -band center that optimizes the adsorption of key intermediates (*CH 2 OHCOOH and *NO). As a result, RuSA/Trp-Co 3 O 4 delivers high Faradaic efficiencies of 94.21% for selective C−C cleavage toward formate synthesis via the EGOR at 1.40 V vs RHE and 88.28% for NH 3 formation via the NO 3 RR at −0.20 V vs RHE. In situ spectroelectrochemistry and theoretical calculations reveal that the synergistic effects of isolated Ru sites suppress EG overoxidation and NO 3 − overreduction, thereby enabling efficient hybrid electrolysis for the concurrent upcycling of NO 3 − and PET hydrolysate into NH 3 and formate, respectively, while simultaneously facilitating the recovery of high-purity terephthalic acid. This work establishes a scalable design strategy for high-utilization single-atom catalysts for coupled waste upcycling reactions.

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