Enzymes Immobilized on Carbon Nitride (C 3 N 4 ) Cooperating with Metal Nanoparticles for Cascade Catalysis

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Yangxin Wang
  • Ningning Zhang
  • René Hübner
  • Deming Tan
  • Markus Löffler
  • Stefan Facsko
  • En Zhang
  • Yan Ge
  • Zhenhui Qi
  • Changzhu Wu

Research Organisations

External Research Organisations

  • Northwestern Polytechnical University
  • Technische Universität Dresden
  • Helmholtz-Zentrum Dresden-Rossendorf (HZDR)
  • University of Southern Denmark
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Details

Original languageEnglish
Article number1801664
Number of pages11
JournalAdvanced materials interfaces
Volume6
Issue number6
Early online date28 Jan 2019
Publication statusPublished - 22 Mar 2019

Abstract

The exploration of effective platforms for immobilizing chemo- and biocatalysts to develop biohybrid catalysts is an attractive subject of practical interest. In this work, carbon nitride (C 3 N 4 ) is used for the first time as a platform for the immobilization of metal catalyst (Pd nanoparticles) and biocatalyst (Candida antarctica lipase B, CalB) in a facile manner to prepare biohybrid catalyst. The optimal biohybrid catalyst inherits the intrinsic performance of both Pd nanoparticles and CalB, and shows high activity in the one-pot cascade reaction converting benzaldehyde to benzyl hexanoate at room temperature. With this proof of concept, it is expected that C 3 N 4 can be utilized for immobilizing more types of chemo- and biocatalysts for perspective applications.

Keywords

    biohybrid catalysts, CalB, carbon nitride, cascade reactions, Pd nanoparticles

ASJC Scopus subject areas

Cite this

Enzymes Immobilized on Carbon Nitride (C 3 N 4 ) Cooperating with Metal Nanoparticles for Cascade Catalysis. / Wang, Yangxin; Zhang, Ningning; Hübner, René et al.
In: Advanced materials interfaces, Vol. 6, No. 6, 1801664, 22.03.2019.

Research output: Contribution to journalArticleResearchpeer review

Wang, Y., Zhang, N., Hübner, R., Tan, D., Löffler, M., Facsko, S., Zhang, E., Ge, Y., Qi, Z., & Wu, C. (2019). Enzymes Immobilized on Carbon Nitride (C 3 N 4 ) Cooperating with Metal Nanoparticles for Cascade Catalysis. Advanced materials interfaces, 6(6), Article 1801664. https://doi.org/10.1002/admi.201801664
Wang Y, Zhang N, Hübner R, Tan D, Löffler M, Facsko S et al. Enzymes Immobilized on Carbon Nitride (C 3 N 4 ) Cooperating with Metal Nanoparticles for Cascade Catalysis. Advanced materials interfaces. 2019 Mar 22;6(6):1801664. Epub 2019 Jan 28. doi: 10.1002/admi.201801664
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abstract = " The exploration of effective platforms for immobilizing chemo- and biocatalysts to develop biohybrid catalysts is an attractive subject of practical interest. In this work, carbon nitride (C 3 N 4 ) is used for the first time as a platform for the immobilization of metal catalyst (Pd nanoparticles) and biocatalyst (Candida antarctica lipase B, CalB) in a facile manner to prepare biohybrid catalyst. The optimal biohybrid catalyst inherits the intrinsic performance of both Pd nanoparticles and CalB, and shows high activity in the one-pot cascade reaction converting benzaldehyde to benzyl hexanoate at room temperature. With this proof of concept, it is expected that C 3 N 4 can be utilized for immobilizing more types of chemo- and biocatalysts for perspective applications.",
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AU - Wang, Yangxin

AU - Zhang, Ningning

AU - Hübner, René

AU - Tan, Deming

AU - Löffler, Markus

AU - Facsko, Stefan

AU - Zhang, En

AU - Ge, Yan

AU - Qi, Zhenhui

AU - Wu, Changzhu

N1 - Funding Information: The authors gratefully acknowledge financial support from the Thousand Talents Program of China (1800-16GH030121), China Postdoctoral Science Foundation (2017M623231), and Fundamental Research Funds for the Central Universities (3102018zy051). C.W. thanks DFG (WU 814/1-1) for financial support. The use of HZDR Ion Beam Center TEM facilities and the funding of TEM Talos by the German Federal Ministry of Education of Research (BMBF, Grant No. 03SF0451) in the framework of HEMCP are acknowledged. M.L. acknowledges support by Deutsche Forschungsgemeinschaft via the cluster of excellence EXC1056 “Center for Advancing Electronics Dresden” (cfaed). The authors thank Matthias Kluge for his assistance with TGA characterization, Mingchao Wang for his assistance with FTIR characterization, and Yujian Zhou for his assistance with ICP-AES characterization. The authors also thank the Analytical and Testing Center of NPU for the characterization instruments. They thank Prof. Marion B. Ansorge-Schumacher (TU Dresden) for valuable discussions and support and Prof. Rainer Jordan (TU Dresden) for providing lab facility.

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