[RhIII(dmbpy)2Cl2]+ as a highly efficient catalyst for visible-light-driven hydrogen production in pure water: Comparison with other rhodium catalysts

Chemistry - A European Journal

Volumn 19, Issue 2, 2013, Pages 782-792

  Stoll, Thibaut ^a   Gennari, Marcello ^a   Serrano, Isabel ^a   Fortage, Jérôme ^a   Chauvin, Jérôme ^a   Odobel, Fabrice ^b   Rebarz, Mateusz ^c   Poizat, Olivier ^c   Sliwa, Michel ^c   Deronzier, Alain ^a   Collomb, Marie Noëlle ^a  

^a UNIV GRENOBLE ALPES   (France)

^b CNRS   (France)

^c UNIVERSITÉ DES SCIENCES ET TECHNOLOGIES DE LILLE   (France)

Author keywords

homogeneous catalysis; hydrogen; photocatalysis; rhodium; water chemistry

Indexed keywords

ACID SYSTEMS; AQUEOUS MEDIUM; COMPARATIVE STUDIES; EFFICIENT CATALYSTS; EVOLUTION MECHANISM; HOMOGENEOUS CATALYSIS; HOMOGENEOUS SYSTEM; NANOSECOND TRANSIENT ABSORPTION; OPTIMAL CONDITIONS; PERFORMANCE LIMITS; PHOTO-CATALYTIC; PHOTOCATALYTIC SYSTEMS; PURE WATER; RHODIUM CATALYSTS; ROOM TEMPERATURE; RU(BPY); SACRIFICIAL ELECTRON DONORS; TURNOVER FREQUENCY; VISIBLE-LIGHT-DRIVEN; WATER CHEMISTRY;

CATALYSTS; HYDROGEN; HYDROGEN PRODUCTION; IRIDIUM; PHOTOCATALYSIS; PHOTOSENSITIZERS; REACTION KINETICS; RHODIUM; SODIUM; SOLUTIONS;

RHODIUM COMPOUNDS;

EID: 84871979517     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202555     Document Type: Article

References (76)

1. T. S. Teets, D. G. Nocera, Chem. Commun. 2011, 47, 9268-9274
2. M. J. Esswein, D. G. Nocera, Chem. Rev. 2007, 107, 4022-4047
3. N. D. McDaniel, S. Bernhard, Dalton Trans. 2010, 39, 10021-10030.
4. B. V. Koriakin, T. S. Dzhabiev, A. E. Shilov, Dokl. Akad. Nauk SSSR 1977, 233, 620-622
5. J. M. Lehn, J. P. Sauvage, Nouv. J. Chim. 1977, 1, 449-451
6. A. Moradpour, E. Amouyal, P. Keller, H. Kagan, Nouv. J. Chim. 1978, 2, 547-549
7. K. Kalyanasundaram, J. Kiwi, M. Gratzel, Helv. Chim. Acta 1978, 61, 2720-2730
8. M. Kirch, J. M. Lehn, J. P. Sauvage, Helv. Chim. Acta 1979, 62, 1345-1384
9. P. J. Delaive, B. P. Sullivan, T. J. Meyer, D. G. Whitten, J. Am. Chem. Soc. 1979, 101, 4007-4008
10. G. M. Brown, B. S. Brunschwig, C. Creutz, J. F. Endicott, N. Sutin, J. Am. Chem. Soc. 1979, 101, 1298-1300
11. G. M. Brown, S. F. Chan, C. Creutz, H. A. Schwarz, N. Sutin, J. Am. Chem. Soc. 1979, 101, 7638-7640
12. B. Durham, W. J. Dressick, T. J. Meyer, J. Chem. Soc. Chem. Commun. 1979, 381-382
13. J. Kiwi, M. Gratzel, J. Am. Chem. Soc. 1979, 101, 7214-7217
14. J. Kiwi, M. Gratzel, Nature 1979, 281, 657-658
15. I. Okura, N. Kimthuan, J. Mol. Catal. 1979, 5, 311-314.
16. S. Rau, D. Walther, J. G. Vos, Dalton Trans. 2007, 915-919
17. M. Wang, Y. Na, M. Gorlov, L. C. Sun, Dalton Trans. 2009, 6458-6467
18. L. L. Tinker, N. D. McDaniel, S. Bernhard, J. Mater. Chem. 2009, 19, 3328-3337
19. S. Losse, J. G. Vos, S. Rau, Coord. Chem. Rev. 2010, 254, 2492-2504
20. V. Artero, M. Chavarot-Kerlidou, M. Fontecave, Angew. Chem. 2011, 123, 7376-7405
21. Angew. Chem. Int. Ed. 2011, 50, 7238-7266
22. P. Du, R. Eisenberg, Energy Environ. Sci. 2012, 5, 6012-6021.
23. B. D. Stubbert, J. C. Peters, H. B. Gray, J. Am. Chem. Soc. 2011, 133, 18070-18073
24. B. Probst, M. Guttentag, A. Rodenberg, P. Hamm, R. Alberto, Inorg. Chem. 2011, 50, 3404-3412
25. M. Guttentag, A. Rodenberg, R. Kopelent, B. Probst, C. Buchwalder, M. Brandstätter, P. Hamm, R. Alberto, Eur. J. Inorg. Chem. 2012, 59-64.
26. C. V. Krishnan, N. Sutin, J. Am. Chem. Soc. 1981, 103, 2141-2142
27. C. V. Krishnan, C. Creutz, D. Mahajan, H. A. Schwarz, N. Sutin, Isr. J. Chem. 1982, 22, 98-106
28. J. R. Fisher, D. J. Cole-Hamilton, J. Chem. Soc. Dalton Trans. 1984, 809-813
29. S. Oishi, J. Mol. Catal. 1987, 39, 225-232
30. U. Kölle, M. Grätzel, Angew. Chem. 1987, 99, 572-574
31. Angew. Chem. Int. Ed. Engl. 1987, 26, 567-570
32. R. Bauer, H. A. F. Werner, Int. J. Hydrogen Energy 1994, 19, 497-499
33. S. Tanaka, S. Masaoka, K. Yamauchi, M. Annaka, K. Sakai, Dalton Trans. 2010, 39, 11218-11226
34. S. Fukuzumi, T. Kobayashi, T. Suenobu, Angew. Chem. 2011, 123, 754-757
35. Angew. Chem. Int. Ed. 2011, 50, 728-731
36. Y. Sano, A. Onoda, T. Hayashi, Chem. Commun. 2011, 47, 8229-8231
37. F. Wang, W.-G. Wang, X.-J. Wang, H.-Y. Wang, C.-H. Tung, L.-Z. Wu, Angew. Chem. 2011, 123, 3251-3255
38. Angew. Chem. Int. Ed. 2011, 50, 3193-3197
39. H. Ozawa, K. Sakai, Chem. Commun. 2011, 47, 2227-2242
40. W. Zhang, J. Hong, J. Zheng, Z. Huang, J. S. Zhou, R. Xu, J. Am. Chem. Soc. 2011, 133, 20680-20683
41. T. M. McCormick, Z. J. Han, D. J. Weinberg, W. W. Brennessel, P. L. Holland, R. Eisenberg, Inorg. Chem. 2011, 50, 10660-10666.
42. W. M. Singh, T. Baine, S. Kudo, S. Tian, X. A. N. Ma, H. Zhou, N. J. DeYonker, T. C. Pham, J. C. Bollinger, D. L. Baker, B. Yan, C. E. Webster, X. Zhao, Angew. Chem. 2012, 124, 6043-6046
43. Angew. Chem. Int. Ed. 2012, 51, 5941-5944.
44. E. Amouyal, P. Koffi, J. Photochem. 1985, 29, 227-242.
45. Mercury is known to form amalgam with colloidal metal or to adsorb to nanoparticular metal catalysts and mercury poisoning has been reported for rhodium colloids. See:, K. Weddle, J. Aiken, R. Finke, J. Am. Chem. Soc. 1998, 120, 5653-5666.
46. C. Caix, S. Chardon-Noblat, A. Deronzier, J. C. Moutet, S. Tingry, J. Organomet. Chem. 1997, 540, 105-111.
47. S. Cosnier, A. Deronzier, N. Vlachopoulos, J. Chem. Soc. Chem. Commun. 1989, 1259-1261
48. S. Chardon-Noblat, S. Cosnier, A. Deronzier, N. Vlachopoulos, J. Electroanal. Chem. 1993, 352, 213-228
49. I. M. F. De Oliveira, J. C. Moutet, N. Vlachopoulos, J. Electroanal. Chem. 1990, 291, 243-249
50. S. Chardon-Noblat, I. M. F. De Oliveira, J. C. Moutet, S. Tingry, J. Mol. Catal. A: Chem. 1995, 99, 13-21.
51. E. D. Cline, S. E. Adamson, S. Bernhard, Inorg. Chem. 2008, 47, 10378-10388
52. S. Metz, S. Bernhard, Chem. Commun. 2010, 46, 7551-7553.
53. A. Fihri, V. Artero, A. Pereira, M. Fontecave, Dalton Trans. 2008, 5567-5569
54. J. I. Goldsmith, W. R. Hudson, M. S. Lowry, T. H. Anderson, S. Bernhard, J. Am. Chem. Soc. 2005, 127, 7502-7510
55. S. Jasimuddin, T. Yamada, K. Fukuju, J. Otsuki, K. Sakai, Chem. Commun. 2010, 46, 8466-8468.
56. P. Zhang, M. Wang, Y. Na, X. Q. Li, Y. Jiang, L. C. Sun, Dalton Trans. 2010, 39, 1204-1206
57. F. Gärtner, A. Boddien, E. Barsch, K. Fumino, S. Losse, H. Junge, D. Hollmann, A. Bruckner, R. Ludwig, M. Beller, Chem. Eur. J. 2011, 17, 6425-6436
58. F. Gärtner, D. Cozzula, S. Losse, A. Boddien, G. Anilkumar, H. Junge, T. Schulz, N. Marquet, A. Spannenberg, S. Gladiali, M. Beller, Chem. Eur. J. 2011, 17, 6998-7006.
59. Z. Han, W. R. McNamara, M.-S. Eum, P. L. Holland, R. Eisenberg, Angew. Chem. 2012, 124, 1699-1702
60. Angew. Chem. Int. Ed. 2012, 51, 1667-1670.
61. J. Van Houten, R. J. Watts, J. Am. Chem. Soc. 1975, 97, 3843-3844.
62. G. Kew, K. DeArmond, K. Hanck, J. Phys. Chem. 1974, 78, 727-734.
63. A. Juris, V. Balzani, F. Barigelletti, S. Campagna, P. Belser, A. Von Zelewsky, Coord. Chem. Rev. 1988, 84, 85-277.
64. F. Prieto, B. A. Coles, R. G. Compton, J. Phys. Chem. B 1998, 102, 7442-7447.
65. C. Creutz, Inorg. Chem. 1981, 20, 4449-4452.
66. C. Creutz, N. Sutin, B. S. Brunschwig, J. Am. Chem. Soc. 1979, 101, 1297-1298.
67. R. Bensasson, C. Sale, V. Balzani, J. Am. Chem. Soc. 1976, 98, 3722-3724
68. N. H. Damrauer, G. Cerullo, A. Yeh, T. R. Boussie, C. V. Shank, J. K. McCusker, Science 1997, 275, 54-57
69. J. K. McCusker, Acc. Chem. Res. 2003, 36, 876-887.
70. M. Chou, C. Creutz, D. Mahajan, N. Sutin, A. P. Zipp, Inorg. Chem. 1982, 21, 3989-3997.
71. S. F. Chan, M. Chou, C. Creutz, T. Matsubara, N. Sutin, J. Am. Chem. Soc. 1981, 103, 369-379
72. N. Sutin, C. Creutz, E. Fujita, Comments Inorg. Chem. 1997, 19, 67-92.
73. S. Fukuzumi, T. Kobayashi, T. Suenobu, ChemSusChem 2008, 1, 827-834.
74. A. F. Borowski, D. J. Cole-Hamilton, G. Wilkinson, Nouv. J. Chim. 1978, 2, 137-144.
75. M. Mauro, K. C. Schuermann, R. Pretot, A. Hafner, P. Mercandelli, A. Sironi, L. De Cola, Angew. Chem. 2010, 122, 1244-1248
76. Angew. Chem. Int. Ed. 2010, 49, 1222-1226.