Plasmon-Driven Urea Photosynthesis on a Rationally Designed RuCu Nanoalloy Cocatalyst Through a Kinetically Favorable C–N Coupling Mechanism
Abstract Photocatalytic urea synthesis from N2 and CO2 offers a sustainable alternative to the energy-intensive industrial process. However, the efficiency remains hindered by the sluggish C–N coupling kinetics. Herein, a new, kinetically favorable urea synthesis pathway is achieved by a rationally designed RuCu alloy/plasmonic WO3–x hybrid photocatalyst. A remarkable urea production rate of 750 μg gcat–1 h–1 together with a solar-to-chemical conversion efficiency of 0.072% is obtained under simulated sunlight illumination, outperforming those of most reported systems. Unlike commonly studied C–N coupling involving *CO and *N2, a new mechanism is proposed. This mechanism activates and reduces N2 and CO2 into the *NH2NH2 and *CO, respectively, followed by two successive C–N coupling processes to form urea with substantially reduced kinetic barriers. The RuCu alloy demonstrates a much lower energy barrier compared to pure metals, which is attributed to its optimized electronic structure and enhanced intermediate adsorption properties enabled by the intersite synergistic effect within the alloy.
Authors
- Xiaoya Qiao (ORCID: https://orcid.org/0000-0001-7226-4054)
- Jianfang F. Wang (ORCID: https://orcid.org/0000-0002-2467-8751)
- Ruibin Jiang (ORCID: https://orcid.org/0000-0001-6977-3421)
- Binbin Chang (ORCID: https://orcid.org/0000-0001-6172-9952)
- Yini Fang (ORCID: https://orcid.org/0009-0008-9478-5545)
- Ke An (ORCID: https://orcid.org/0000-0003-3136-4600)
- Boyuan Wu
- Baocheng Yang
- Penglei Wang
Institutions
- Chinese University of Hong Kong (HK)
- Shaanxi Normal University (CN)
- Taiyuan University of Technology (CN)
- Huanghe Science and Technology College (CN)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-10-07
- DOI
- https://doi.org/10.1021/jacs.6c18367
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00