Year: 2025
Type: article
Abstract: Solar reforming uses sunlight to valorize waste and offers a promising route to circular chemistry, but most current systems operate under corrosive conditions, lack scalability and processability, or suffer from poor selectivity in oxidative waste valorization. Here, a modular composite photocatalyst, comprising a crystalline covalent organic framework (COF), cyanamide‐functionalized carbon nitride (CN x ), indium tin oxide (ITO), and a nickel‐based molecular catalyst (NiME), capable of driving selective waste valorization and H 2 generation using visible light under pH neutral aqueous conditions is reported. The porous structure of the COF provides nanoconfinement, thereby supporting the targeted oxidation of polyols and sugars into formate (HCOO − ), while carbon nitride in the presence of the molecular catalyst facilitates H 2 evolution. ITO functions as a solid‐state electron mediator, enabling coupled oxidative and reductive processes for the concurrent solar‐driven production of H 2 and HCOO − . The high processability of the COF|ITO|CN x |NiME composite allows for the construction of a standalone photoleaf and photopanel, which have been integrated into a single‐window and a scalable multi‐window reactor, respectively. Continuous operability over seven days, along with testing under outdoor conditions with pretreated plastic under direct sunlight, offers a pathway toward practical and scalable solar reforming using structurally tunable organic semiconductor composites.
Source: Advanced Materials
Institution: University of Cambridge
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $6,070
OpenAlex ID: W4414557040