Copper-Modified Covalent Triazine Frameworks as Non-Noble-Metal Electrocatalysts for Oxygen Reduction

Angewandte Chemie - International Edition

Volumn 54, Issue 38, 2015, Pages 11068-11072

  Iwase, Kazuyuki ^a   Yoshioka, Tatsuro ^a   Nakanishi, Shuji ^a   Hashimoto, Kazuhito ^a   Kamiya, Kazuhide ^a,b  

^a UNIVERSITY OF TOKYO   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

copper; electrocatalysis; fuel cells; nanostructures; oxygen reduction

Indexed keywords

COPPER; COPPER COMPOUNDS; ELECTROCATALYSIS; ELECTROCATALYSTS; ELECTRODES; ELECTROLYSIS; ELECTROLYTIC REDUCTION; FUEL CELLS; NANOSTRUCTURES; OXYGEN; PRECIOUS METALS; SYNTHESIS (CHEMICAL);

CARBON NANO-PARTICLES; CATHODE REACTIONS; COVALENTLY CROSS-LINKED; ELECTROCHEMICAL OXYGEN REDUCTION; MOLECULAR COMPLEXES; NEUTRAL SOLUTION; OXYGEN REDUCTION; REVERSIBLE HYDROGEN ELECTRODES;

OXYGEN REDUCTION REACTION;

EID: 84973657594     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201503637     Document Type: Article

References (52)

1. B. E. Logan, B. Hamelers, R. A. Rozendal, U. Schrorder, J. Keller, S. Freguia, P. Aelterman, W. Verstraete, K. Rabaey, Environ. Sci. Technol. 2006, 40, 5181–5192;
2. A. Heller, Phys. Chem. Chem. Phys. 2004, 6, 209–216;
3. S. Calabrese Barton, J. Gallaway, P. Atanassov, Chem. Rev. 2004, 104, 4867–4886;
4. F. Zhao, R. C. T. Slade, J. R. Varcoe, Chem. Soc. Rev. 2009, 38, 1926–1939.
5. L. Feng, Y. Chen, L. Chen, ACS Nano 2011, 5, 9611–9618;
6. F. Harnisch, U. Schroeder, Chem. Soc. Rev. 2010, 39, 4433–4448;
7. L. Birry, P. Mehta, F. Jaouen, J. P. Dodelet, S. R. Guiot, B. Tartakovsky, Electrochim. Acta 2011, 56, 1505–1511.
8. H. B. Gray, B. G. Malmstrom, R. J. P. Williams, J. Biol. Inorg. Chem. 2000, 5, 551–559.
9. N. Mano, V. Soukharev, A. Heller, J. Phys. Chem. B 2006, 110, 11180–11187.
10. E. I. Solomon, D. E. Heppner, E. M. Johnston, J. W. Ginsbach, J. Cirera, M. Qayyum, M. T. Kieber-Emmons, C. H. Kjaergaard, R. G. Hadt, L. Tian, Chem. Rev. 2014, 114, 3659–3853.
11. M. S. Thorum, J. Yadav, A. A. Gewirth, Angew. Chem. Int. Ed. 2009, 48, 165–167;
12. Angew. Chem. 2009, 121, 171–173.
13. M. A. Thorseth, C. S. Letko, E. C. M. Tse, T. B. Rauchfuss, A. A. Gewirth, Inorg. Chem. 2013, 52, 628–634.
14. V. L. N. Dias, E. N. Fernandes, L. M. S. da Silva, E. P. Marques, J. J. Zhang, A. L. B. Marques, J. Power Sources 2005, 142, 10–17;
15. C. C. L. McCrory, X. Ottenwaelder, T. D. P. Stack, C. E. D. Chidsey, J. Phys. Chem. A 2007, 111, 12641–12650;
16. K. Slowiński, Z. Kublik, R. Bilewicz, M. Pietraszkiewicz, J. Chem. Soc. Chem. Commun. 1994, 1087–1088.
17. M. A. Thorseth, C. E. Tornow, E. C. M. Tse, A. A. Gewirth, Coord. Chem. Rev. 2013, 257, 130–139.
18. S. Y. Ding, W. Wang, Chem. Soc. Rev. 2013, 42, 548–568;
19. X. Feng, X. S. Ding, D. L. Jiang, Chem. Soc. Rev. 2012, 41, 6010–6022;
20. P. Kuhn, M. Antonietti, A. Thomas, Angew. Chem. Int. Ed. 2008, 47, 3450–3453;
21. Angew. Chem. 2008, 120, 3499–3502;
22. P. Kuhn, A. Forget, D. S. Su, A. Thomas, M. Antonietti, J. Am. Chem. Soc. 2008, 130, 13333–13337;
23. K. Sakaushi, M. Antonietti, Bull. Chem. Soc. Jpn. 2015, 88, 386–398.
24. K. Kamiya, R. Kamai, K. Hashimoto, S. Nakanishi, Nat. Commun. 2014, 5, 5040.
25. X. F. Yang, A. Q. Wang, B. T. Qiao, J. Li, J. Y. Liu, T. Zhang, Acc. Chem. Res. 2013, 46, 1740–1748.
26. F. Calle-Vallejo, D. Loffreda, M. T. M. Koper, P. Sautet, Nat. Chem. 2015, 7, 403–410.
27. C. E. Chan-Thaw, A. Villa, G. M. Veith, K. Kailasam, L. A. Adamczyk, R. R. Unocic, L. Prati, A. Thomas, Chem. Asian J. 2012, 7, 387–393;
28. J. Roeser, K. Kailasam, A. Thomas, ChemSusChem 2012, 5, 1793–1799.
29. H. Irie, K. Kamiya, T. Shibanuma, S. Miura, D. A. Tryk, T. Yokoyama, K. Hashimoto, J. Phys. Chem. C 2009, 113, 10761–10766.
30. G. G. Jernigan, G. A. Somorjai, J. Catal. 1994, 147, 567–577;
31. J. L. Du, Z. F. Chen, S. R. Ye, B. J. Wiley, T. J. Meyer, Angew. Chem. Int. Ed. 2015, 54, 2073–2078;
32. Angew. Chem. 2015, 127, 2101–2106;
33. V. Hayez, A. Franquet, A. Hubin, H. Terryn, Surf. Interface Anal. 2004, 36, 876–879.
34. N. Kitajima, Y. Morooka, Chem. Rev. 1994, 94, 737–757;
35. C. C. L. McCrory, A. Devadoss, X. Ottenwaelder, R. D. Lowe, T. D. P. Stack, C. E. D. Chidsey, J. Am. Chem. Soc. 2011, 133, 3696–3699.
36. A. K. Churg, A. Warshel, Biochemistry 1986, 25, 1675–1681;
37. F. A. Tezcan, J. R. Winkler, H. B. Gray, J. Am. Chem. Soc. 1998, 120, 13383–13388.
38. H. Alt, H. Binder, G. Sandsted, J. Catal. 1973, 28, 8–19.
39. P. Vasudevan, Santosh, N. Mann, S. Tyagi, Transition Met. Chem. 1990, 15, 81–90.
40. K. K. Tanabe, M. S. Ferrandon, N. A. Siladke, S. J. Kraft, G. H. Zhang, J. Niklas, O. G. Poluektov, S. J. Lopykinski, E. E. Bunel, T. R. Krause, J. T. Miller, A. S. Hock, S. T. Nguyen, Angew. Chem. Int. Ed. 2014, 53, 12055–12058;
41. Angew. Chem. 2014, 126, 12251–12254;
42. K. K. Tanabe, N. A. Siladke, E. M. Broderick, T. Kobayashi, J. F. Goldston, M. H. Weston, O. K. Farha, J. T. Hupp, M. Pruski, E. A. Mader, M. J. A. Johnson, S. T. Nguyen, Chem. Sci. 2013, 4, 2483–2489;
43. J. M. Thomas, R. Raja, D. W. Lewis, Angew. Chem. Int. Ed. 2005, 44, 6456–6482;
44. Angew. Chem. 2005, 117, 6614–6641.
45. F. Calle-Vallejo, M. T. M. Koper, A. S. Bandarenka, Chem. Soc. Rev. 2013, 42, 5210–5230;
46. J. Greeley, I. E. L. Stephens, A. S. Bondarenko, T. P. Johansson, H. A. Hansen, T. F. Jaramillo, J. Rossmeisl, I. Chorkendorff, J. K. Norskov, Nat. Chem. 2009, 1, 552–556;
47. A. U. Nilekar, M. Mavrikakis, Surf. Sci. 2008, 602, L89–L94;
48. L. Yang, M. B. Vukmirovic, D. Su, K. Sasaki, J. A. Herron, M. Mavrikakis, S. Liao, R. R. Adzic, J. Phys. Chem. C 2013, 117, 1748–1753;
49. J. L. Zhang, M. B. Vukmirovic, Y. Xu, M. Mavrikakis, R. R. Adzic, Angew. Chem. Int. Ed. 2005, 44, 2132–2135;
50. Angew. Chem. 2005, 117, 2170–2173.
51. J. Artz, S. Mallmann, R. Palkovits, ChemSusChem 2015, 8, 672–679;
52. X. Zhu, C. Tian, S. M. Mahurin, S.-H. Chai, C. Wang, S. Brown, G. M. Veith, H. Luo, H. Liu, S. Dai, J. Am. Chem. Soc. 2012, 134, 10478–10484.