2D/2D CdS/1T-MoS2 heterojunctions with abundant interfacial sulfur vacancies for high-efficient photocatalytic amino acid synthesis from bio-based feedstocks
Photocatalytic amino acid synthesis from biomass is a promising and renewable method, yet the synthesis efficiency remains suboptimal. Here, we report a novel strategy for synthesizing 2D/2D CdS/1T-MoS 2 heterojunctions by leveraging 1T-phase MoS 2 with distorted octahedral coordination and sulfur-rich edges to promote the formation of large contact areas and abundant interfacial sulfur vacancies in combination with CdS. CdS/1T-MoS 2 displays exceptional photocatalytic performance for amination of biomass-derived α-hydroxy acids to α-amino acids, achieving an alanine formation rate of 23.3 mmol·g −1 ·h −1 from lactic acid, which is 4.4 and 1.6 times higher than those of CdS and CdS/2H-MoS 2 , respectively. Detailed characterizations reveal that CdS/1T-MoS 2 possesses abundant interfacial sulfur vacancies at the 2D/2D heterojunction interface compared to CdS and CdS/2H-MoS 2 . These vacancies create numerous Lewis acids sites, significantly enhancing the adsorption and activation of hydroxyl groups in lactic acid, thereby promoting the dehydrogenation step. Moreover, CdS/1T-MoS 2 facilitates the condensation of pyruvic acid with ammonia and promotes the desorption of alanine from the catalyst surface, effectively improving the reductive amination step. Additionally, CdS/1T-MoS 2 exhibits superior charge carrier separation and migration efficiency, further boosting its photocatalytic amination activity. This study provides a novel strategy for synthesizing 2D/2D heterojunctions with abundant interfacial vacancies for efficient photocatalytic biomass valorization. 2D/2D CdS/1T-MoS 2 heterojunctions with abundant interfacial sulfur vacancies for high-efficient photocatalytic amino acid synthesis from bio-based feedstocks. • A two-step solvothermal strategy to synthesize 2D/2D CdS/1T-MoS 2 heterojunctions with interfacial S vacancies. • Interfacial sulfur vacancies are favorable for the adsorption and activation of the hydroxy group in the lactic acid. • 2D/2D CdS/1T-MoS 2 enhances photocatalytic activity via improved charge carrier separation and migration.
Authors
- Maofeng Ding
- Licai Hao (ORCID: https://orcid.org/0000-0002-0637-5132)
- Song Song (ORCID: https://orcid.org/0000-0002-0216-3941)
- Xingang Li (ORCID: https://orcid.org/0000-0002-8226-9796)
- Yong You (ORCID: https://orcid.org/0000-0002-4689-0235)
Institutions
- Tianjin University (CN)
- Shaoxing University (CN)
- State Key Laboratory of Chemical Engineering (CN)
Publication Details
- Journal
- Applied Catalysis B: Environmental
- Published
- 2025-04-14
- DOI
- https://doi.org/10.1016/j.apcatb.2025.125371
- Citations
- 17
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 6.18
Funders
- National Natural Science Foundation of China