Skip to main content

Advertisement

Log in

Rational construction of Co-promoted 1T-MoS2 nanoflowers towards high-efficiency 4-nitrophenol reduction

  • Research Article
  • Published:
Environmental Science and Pollution Research Aims and scope Submit manuscript

Abstract

Developing efficient and cost-effective non-noble metal catalysts for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) is of great importance. Herein, Co-promoted 1T-MoS2 nanoflowers were synthesized via a one-step hydrothermal method. The influence of Co content on the structure and catalytic performance of 1T-MoS2 was studied in detail. It was found that Co doping not only enhanced the electronic conductivity but also increased the hydrogen adsorption ability of 1T-MoS2. Meanwhile, the highest activity was achieved due to the synergy effect of Co-Mo-S and CoS2 active phase. In the catalytic reduction of 4-NP, the reaction rate constant of Co/1T-MoS2-0.3 was as high as 0.908 min−1 and the catalyst exhibited excellent stability after recycling five times. The present work provides new insights for the rational design of highly efficient metal-doped MoS2 catalysts towards 4-NP reduction in wastewater.

Graphical abstract

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Scheme 1
Scheme 2
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

Data availability

All data during this study are included in this article.

References

Download references

Funding

This work was financially supported by the National Natural Science Foundation of China (Grant No. 22102055), Natural Science Foundation of Hunan Province (Grant No. 2021JJ40222), the Scientific Research Fund of Hunan Provincial Education Department (Grant No. 20B264), and the Undergraduate Innovation and Entrepreneurship Training Program of Hunan Institute of Science and Technology.

Author information

Authors and Affiliations

Authors

Contributions

All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by Cen Zhang, Li Wang, Xi Huang, Liang Bai, Qiyuan Yu, Bin Jiang, and Chenlu Zheng. The first draft of the manuscript was written by Jing Cao, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Jing Cao.

Ethics declarations

Ethics approval

Not applicable.

Consent to participate

Not applicable.

Consent for publication

Not applicable.

Conflict of interest

The authors declare no competing interests.

Additional information

Responsible Editor: George Z. Kyzas

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Highlights

• Co-promoted 1T-MoS2 nanoflowers were synthesized by a facile one-pot hydrothermal method.

• The optimized Co/1T-MoS2 catalyst showed excellent catalytic activity and stability in the reduction of 4-nitrophenol.

• The excellent catalytic performance was attributed to the synergism between Co-Mo-S and CoS2 active phase.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 7482 KB)

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhang, C., Wang, L., Huang, X. et al. Rational construction of Co-promoted 1T-MoS2 nanoflowers towards high-efficiency 4-nitrophenol reduction. Environ Sci Pollut Res 30, 11811–11822 (2023). https://doi.org/10.1007/s11356-022-22974-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11356-022-22974-1

Keywords

Navigation