4.6 Article

Self-Assembly of Porphyrin Dipeptide Conjugates toward Hydrogen Production

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 23, 页码 7781-7791

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.1c00978

关键词

self-assembly; hydrogen production; porphyrin; diphenylalanine

资金

  1. General Secretariat for Research and Technology (GSRT)
  2. Hellenic Foundation for Research and Innovation [508]
  3. European Union
  4. Greek national funds through the Operational Program Competitiveness, Entrepreneurship, and Innovation under the call RESEARCH-CREATE-INNOVATE [T1EDK-01504]
  5. Greek national funds through the Regional Operational Program Crete 2014-2020'' [OPS:5029187]
  6. European Commission's Seventh Framework Programme (FP7/2007-2013) [229927]
  7. Special Research Account of the University of Crete
  8. IPTO (Independent Power Transmission Operator, A.MHE) scholarship
  9. project Materials and Processes for Energy and Environment Applications - Operational Programme. Competitiveness, Entrepreneurship and Innovation. (NSRF 2014-2020) [MIS 5002556]
  10. European Union (European Regional Development Fund)
  11. European Union's Horizon 2020 research and innovation programme [871124]
  12. HELLAS-CH national infrastructure [MIS 5002735]

向作者/读者索取更多资源

In this research, diphenylalanine dipeptide was covalently attached to a tripyridyl porphyrin macrocycle, imparting self-assembling properties to the resulting hybrid used for non-noble metal photocatalytic hydrogen evolution studies. The self-assembling nanostructures of the hybrid were found to enhance hydrogen production in the photocatalytic system. This was supported by fluorescence and transient absorption experiments shedding light on electron transfer processes during photocatalysis.
In this work, the diphenylalanine dipeptide was covalently attached to a tripyridyl porphyrin macrocycle and conveyed self-assembling properties to the resulting hybrid. This hybrid was metallated with non-noble metals, Zn and Sn, and investigated toward photocatalytic hydrogen evolution. The Sn derivative, SnPy3P-FF, was able to produce hydrogen photo-catalytically in the presence of a known cobaloxime catalyst and TEOA as a sacrificial electron donor. When the self-assembling nanostructures of SnPy3P-FF were employed in the photocatalytic system, enhanced hydrogen production was observed. Fluorescence and transient absorption experiments were performed in order to shed light on the electron transfer processes that take place during the photocatalysis.

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