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.

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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

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article

2D/2D CdS/1T-MoS2 heterojunctions with abundant interfacial sulfur vacancies for high-efficient photocatalytic amino acid synthesis from bio-based feedstocks

Maofeng Ding, Licai Hao, Song Song, Xingang Li et al.
17 citations
Applied Catalysis B: Environmental
Advanced Photocatalysis Techniques
6.18
article

2D/2D CdS/1T-MoS2 heterojunctions with abundant interfacial sulfur vacancies for high-efficient photocatalytic amino acid synthesis from bio-based feedstocks

Maofeng Ding, Licai Hao, Song Song, Xingang Li, Yong You
article en
17 citations

Abstract

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.

Applied Catalysis B: EnvironmentalVol. 374
Tianjin University (CN), Shaoxing University (CN), State Key Laboratory of Chemical Engineering (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 3%
Advanced Photocatalysis Techniques
6.18
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