Single Atom Cu‐Mediated Efficient Z‐Scheme Photocatalytic CO <sub>2</sub> Conversion of TiO <sub>2</sub> Hetero‐Phase Assembly
Constructing metal single-atom-mediated Z-scheme charge transmission is a promising yet challenging avenue to realize efficient solar photocatalysis. Here, a single-atom Cu-bridged TiO<sub>2</sub> hetero-phase assembly with opened cavities and Z-scheme charge transmission is fabricated via the illumination-assisted preparation recipe. When tested for gas-solid photocatalytic CO<sub>2</sub> conversion, our photocatalyst displays an extraordinary activity with CH<sub>4</sub> production rate reaching to 327.19 µmol·g<sup>-1</sup>·h<sup>-1</sup>, roughly 15.6 and 122.1 times enhancement than Degussa P25 TiO<sub>2</sub> and TiO<sub>2</sub>(B), and it outperforms those of Cu nanoparticles, Pd single atoms, Pt nanoparticles, Pd nanoparticles, and Au nanoparticles-loaded counterparts as well as most TiO<sub>2</sub>-based composites ever reported. Based on the experimental test and theoretical calculation results, Cu single atoms act as the mediator to enhance interfacial charge transfer, which changes the photo-carrier transmission pathway from type-II to Z-scheme, accounting for the significant promotion of photocatalytic capability. The study results could propel the marked optimization of photocatalytic efficiency by steering Z-scheme charge transport with a single-atom mediator.
Authors
- V. Z. Turkevich (ORCID: https://orcid.org/0000-0002-1441-4269)
- Zhe Wu (ORCID: https://orcid.org/0000-0001-5552-4619)
- Yang Li (ORCID: https://orcid.org/0009-0009-6927-7271)
- Jie Xu (ORCID: https://orcid.org/0000-0002-1579-0338)
- Yuanxin Qiu
- Haifeng Lin
- Li Wang
- Xun Wang
- Lei Wang
Institutions
- Qingdao University of Science and Technology (CN)
- V. Bakul Institute for Superhard Materials (UA)
- Tsinghua University (CN)
Publication Details
- Journal
- Small
- Published
- 2026-03-09
- DOI
- https://doi.org/10.1002/smll.202514920
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00