Пожалуйста, помогите статьями:
1. J. Am. Chem. Soc., 2006, 128 (44), pp 14256–14257
Renzhi Li†‡, Xueju Lv†, Dong Shi†, Difei Zhou†‡, Yueming Cheng†, Guangliang Zhang*† and Peng Wang*†
Dye-Sensitized Solar Cells Based on Organic Sensitizers with Different Conjugated Linkers: Furan, Bifuran, Thiophene, Bithiophene, Selenophene, and Biselenophene
Код: Выделить всё
http://dx.doi.org/10.1021/jp900972vHyunwoong Park,† Eunyoung Bae,† Jae-Joon Lee,§ Jaiwook Park,‡ and Wonyong Choi*†‡
Effect of the Anchoring Group in Ru−Bipyridyl Sensitizers on the Photoelectrochemical Behavior of Dye-Sensitized TiO2 Electrodes: Carboxylate versus Phosphonate Linkages
Код: Выделить всё
http://dx.doi.org/10.1021/jp060397eHiroshi Imahori*†‡§, Tomokazu Umeyama‡ and Seigo Ito
Large π-Aromatic Molecules as Potential Sensitizers for Highly Efficient Dye-Sensitized Solar Cells
Код: Выделить всё
http://dx.doi.org/10.1021/ar900034tDaniel P. Hagberg, Xiao Jiang, Erik Gabrielsson, Mats Linder, Tannia Marinado, Tore Brinck, Anders Hagfeldt and Licheng Sun
Symmetric and unsymmetric donor functionalization. comparing structural and spectral benefits of chromophores for dye-sensitized solar cell
Код: Выделить всё
http://dx.doi.org/10.1039/b911397pKannan Muthukumaran,† Robert S. Loewe,† Arounaguiry Ambroise,† Shun-ichi Tamaru,† Qiliang Li,‡ Guru Mathur,‡ David F. Bocian,*§ Veena Misra,*‡ and Jonathan S. Lindsey*
Porphyrins Bearing Arylphosphonic Acid Tethers for Attachment to Oxide Surfaces
Код: Выделить всё
http://dx.doi.org/10.1021/jo034945l
