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10.3390/ma9030137 http://scihub22266oqcxt.onion/10.3390/ma9030137 C5456731!5456731!28773266     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Materials+(Basel) 2016 ; 9 (3): ä Nephropedia Template TP {{tp|p=28773266|t=2016. Terpyridine and Quaterpyridine Complexes as Sensitizers for Photovoltaic Applications |pdf=|usr=}}{{28773266}} gab.com Text Terpyridine and Quaterpyridine Complexes as Sensitizers for Photovoltaic Applications JO: Materials (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=28773266 #FOAvip Terpyridine and quaterpyridine-based complexes allow wide light harvesting of the solar spectrum. Terpyridines, with respect to bipyridines, allow for achieving metal-complexes with lower band gaps in the metal-to-ligand transition (MLCT), thus providing a better absorption at lower energy wavelengths resulting in an enhancement of the solar light-harvesting ability. Despite the wider absorption of the first tricarboxylate terpyridyl ligand-based complex, Black Dye (BD), dye-sensitized solar cell (DSC) performances are lower if compared with N719 or other optimized bipyridine-based complexes. To further improve BD performances several modifications have been carried out in recent years affecting each component of the complexes: terpyridines have been replaced by quaterpyridines; other metals were used instead of ruthenium, and thiocyanates have been replaced by different pinchers in order to achieve cyclometalated or heteroleptic complexes. The review provides a summary on design strategies, main synthetic routes, optical and photovoltaic properties of terpyridine and quaterpyridine ligands applied to photovoltaic, and focuses on n-type DSCs. Twit Text FOAVip Terpyridine and Quaterpyridine Complexes as Sensitizers for Photovoltaic Applications ????Materials (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=28773266 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28773266 #FOAvip English Wikipedia <ref>{{Cite pmid|28773266}}</ref> Terpyridine and Quaterpyridine Complexes as Sensitizers for Photovoltaic Applications #MMPMID28773266 Saccone D; Magistris C; Barbero N; Quagliotto P; Barolo C; Viscardi G Materials (Basel) 2016[Mar]; 9 (3): ä PMID28773266show ga Terpyridine and quaterpyridine-based complexes allow wide light harvesting of the solar spectrum. Terpyridines, with respect to bipyridines, allow for achieving metal-complexes with lower band gaps in the metal-to-ligand transition (MLCT), thus providing a better absorption at lower energy wavelengths resulting in an enhancement of the solar light-harvesting ability. Despite the wider absorption of the first tricarboxylate terpyridyl ligand-based complex, Black Dye (BD), dye-sensitized solar cell (DSC) performances are lower if compared with N719 or other optimized bipyridine-based complexes. To further improve BD performances several modifications have been carried out in recent years affecting each component of the complexes: terpyridines have been replaced by quaterpyridines; other metals were used instead of ruthenium, and thiocyanates have been replaced by different pinchers in order to achieve cyclometalated or heteroleptic complexes. The review provides a summary on design strategies, main synthetic routes, optical and photovoltaic properties of terpyridine and quaterpyridine ligands applied to photovoltaic, and focuses on n-type DSCs. äTerpyridine and Quaterpyridine Complexes as Sensitizers for Photovolta(epmc).pdf DeepDyve Pubget Overpricing