Light‐Driven Coupled Upcycling of Polyethylene and CO <sub>2</sub> to Aromatics over Zeolite–Ni/CeO <sub>2</sub> Composite Catalysts
Coupled upcycling of polyolefins and CO 2 into valuable chemicals is a promising waste management strategy, but conventional thermocatalysis requires harsh conditions and high energy input. Here, we report a light‐driven photothermal tandem catalyst of Zn/ZSM‐5 and Ni/CeO 2 for efficient coconversion of low‐density polyethylene (LDPE) and CO 2 . The highly dispersed Ni/CeO 2 component delivers strong light‐to‐heat conversion and abundant Ni–O–Ce interfacial oxygen vacancies for CO 2 activation. Under illumination, Zn/ZSM‐5 catalyzes LDPE C–C cleavage and aromatization, generating active hydrogen species. Simultaneously, Ni/CeO 2 then consumes hydrogen via reverse water‐gas shift, suppressing alkene hydrogenation and promoting aromatics formation. The photothermal catalytic system achieves 82.4% LDPE conversion and 34% aromatic selectivity. This work provides an energy‐efficient, solar‐driven route for plastic and CO 2 upcycling toward carbon‐neutral chemical recycling.
Authors
- Zhiyi Wu (ORCID: https://orcid.org/0009-0007-9005-2304)
- Yihe Huang (ORCID: https://orcid.org/0000-0002-5514-0460)
- Kai Feng (ORCID: https://orcid.org/0000-0003-3697-6139)
- Xingda An (ORCID: https://orcid.org/0000-0002-7484-7410)
- Jiahui Shen (ORCID: https://orcid.org/0000-0003-2531-7752)
- Le He (ORCID: https://orcid.org/0000-0002-4520-0482)
- Weiwei Li (ORCID: https://orcid.org/0000-0002-7329-4236)
- Liu Cao (ORCID: https://orcid.org/0000-0002-6560-154X)
- Chaoran Li (ORCID: https://orcid.org/0000-0001-9517-8431)
- Yuxuan Zhou (ORCID: https://orcid.org/0000-0003-1889-747X)
- Q Feng
- Ning Zhang
- Xiaohan Jin
Institutions
- University of Science and Technology of China (CN)
- Suzhou University of Science and Technology (CN)
- Soochow University (CN)
Publication Details
- Journal
- ChemSusChem
- Published
- 2026-06-13
- DOI
- https://doi.org/10.1002/cssc.70802
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00