journal article·2013-01-22

Knitting the Catalytic Pattern of Artificial Photosynthesis to a Hybrid Graphene Nanotexture

Mildred Quintana, Alejandro Montellano López, Stefania Rapino, Francesca Maria Toma, Matteo Iurlo, Mauro Carraro, Andrea Sartorel, Chiara Maccato, Xiaoxing Ke, Carla Bittencourt, Tatiana Da Ros, Gustaaf Van Tendeloo, Massimo Marcaccio, Francesco Paolucci, Maurizio Prato, Marcella Bonchio

ACS Nano· Volume 7· Issue 1
Publisher page

Abstract

The artificial leaf project calls for new materials enabling multielectron catalysis with minimal overpotential, high turnover frequency, and long-term stability. Is graphene a better material than carbon nanotubes to enhance water oxidation catalysis for energy applications? Here we show that functionalized graphene with a tailored distribution of polycationic, quaternized, ammonium pendants provides an sp(2) carbon nanoplatform to anchor a totally inorganic tetraruthenate catalyst, mimicking the oxygen evolving center of natural PSII. The resulting hybrid material displays oxygen evolution at overpotential as low as 300 mV at neutral pH with negligible loss of performance after 4 h testing. This multilayer electroactive asset enhances the turnover frequency by 1 order of magnitude with respect to the isolated catalyst, and provides a definite up-grade of the carbon nanotube material, with a similar surface functionalization. Our innovation is based on a noninvasive, synthetic protocol for graphene functionalization that goes beyond the ill-defined oxidation-reduction methods, allowing a definite control of the surface properties.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Center of Excellence for Nanostructured Materials (CENMAT) and INSTM, unit of Trieste, Dipartimento di Scienze Chimiche e Farmaceutiche, University of Trieste, Piazzale Europa 1, I-34127 Trieste, Italy

Dipartimento di Chimica “G. Ciamician” and INSTM, unit of Bologna, University of Bologna, Via F. Selmi 2, 40126 Bologna, Italy

ITM-CNR and Dipartimento di Scienze Chimiche, University of Padova, via F. Marzolo 1, 35131 Padova, Italy

EMAT, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium

References (40)

Show source-provided references
1. Faraday Discuss. · 2012 · 155 · 110.1039/c1fd90058g ↗
2. Tran P. D. · Energy Environ. Sci. · 2012 · 5 · 590210.1039/c2ee02849b ↗
3. Umena Y. · Nature · 2011 · 473 · 5510.1038/nature09913 ↗
4. Gray H. B. · Nat. Chem. · 2009 · 1 · 710.1038/nchem.141 ↗
5. Hammarström L. · Energy Environ. Sci. · 2011 · 4 · 233910.1039/c1ee90023d ↗
6. Tachibana Y. · Nat. Photonics · 2012 · 6 · 51110.1038/nphoton.2012.175 ↗
7. Du P. · Energy Environ. Sci. · 2012 · 5 · 601210.1039/c2ee03250c ↗
8. Dau H. · ChemCatChem · 2010 · 2 · 72410.1002/cctc.201000126 ↗
9. Sartorel A. · Energy Environ. Sci. · 2012 · 5 · 559210.1039/c2ee02838g ↗
10. Hocking R. K. · Nat. Chem. · 2011 · 3 · 46110.1038/nchem.1049 ↗
11. Mola J. · Angew. Chem., Int. Ed. · 2008 · 47 · 583010.1002/anie.200704912 ↗
12. deKrafft K. E. · ACS Appl. Mater. Interfaces · 2012 · 4 · 60810.1021/am2018095 ↗
13. Toma F. M. · Nat. Chem. · 2010 · 2 · 82610.1038/nchem.761 ↗
14. Toma F. M. · ChemSusChem · 2011 · 4 · 144710.1002/cssc.201100089 ↗
15. Li F. · Angew. Chem., Int. Ed. · 2011 · 50 · 1227610.1002/anie.201105044 ↗
16. Wu J. · Nano Res. · 2012 · 5 · 52110.1007/s12274-012-0237-y ↗
17. Brownson D. A. C. · Chem. Soc. Rev. · 2012 · 41 · 694410.1039/c2cs35105f ↗
18. Wei W. · Small · 2012 · 8 · 213810.1002/smll.201200104 ↗
19. Luo B. · Small · 2012 · 8 · 63010.1002/smll.201101396 ↗
20. Huang X. · Chem. Soc. Rev. · 2012 · 41 · 66610.1039/C1CS15078B ↗
21. Xiang Q. J. · Chem. Soc. Rev. · 2012 · 41 · 78210.1039/C1CS15172J ↗
22. Sun Y. · En. Env. Sci. · 2011 · 4 · 111310.1039/c0ee00683a ↗
23. Quintana M. · Chem. Commun. · 2011 · 47 · 933010.1039/c1cc13254g ↗
24. 10.1021/ar300138e10.1021/ar300138e ↗
25. Sartorel A. · J. Am. Chem. Soc. · 2008 · 130 · 500610.1021/ja077837f ↗
26. Geletii Y. V. · Angew. Chem., Int. Ed. · 2008 · 47 · 389610.1002/anie.200705652 ↗
27. Sartorel A. · J. Am. Chem. Soc. · 2009 · 131 · 1605110.1021/ja905067u ↗
28. Geletii Y. V. · J. Am. Chem. Soc. · 2009 · 131 · 1736010.1021/ja907277b ↗
29. Natali M. · Inorg. Chem. · 2012 · 51 · 732410.1021/ic300703f ↗
30. Orlandi M. · Chem. Commun. · 2010 · 46 · 315210.1039/b926823e ↗
31. Güell A. G. · J. Am. Chem. Soc. · 2012 · 134 · 725810.1021/ja3014902 ↗
32. Chen D. · Chem. Rev. · 2012 · 112 · 602710.1021/cr300115g ↗
33. Loh K. P. · Nat. Chem. · 2010 · 2 · 101510.1038/nchem.907 ↗
34. Quintana M. · ACS Nano · 2010 · 4 · 352710.1021/nn100883p ↗
35. Montellano López A. · Org. Lett. · 2012 · 14 · 445010.1021/ol301946r ↗
36. Carraro M. · Angew. Chem., Int. Ed. · 2008 · 47 · 727510.1002/anie.200801629 ↗
37. Sartorel A. · Chem. Commun. · 2011 · 47 · 171610.1039/c0cc04366d ↗
38. Costentin C. · J. Am. Chem. Soc. · 2012 · 134 · 1123510.1021/ja303560c ↗
39. Hernandez Y. · Nat. Nanotechnol. · 2008 · 3 · 56310.1038/nnano.2008.215 ↗
40. Milic D. · Eur. J. Org. Chem. · 2010 · 3 · 47610.1002/ejoc.200900791 ↗