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Enabling Efficient Creation of Long-Lived Charge-Separation on Dye-Sensitized NiO Photocathodes
Author(s) -
Robert J. Dillon,
Leila Alibabaei,
Thomas J. Meyer,
John M. Papanikolas
Publication year - 2017
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.7b05856
Subject(s) - materials science , non blocking i/o , charge (physics) , separation (statistics) , dye sensitized solar cell , optoelectronics , nanotechnology , chemical engineering , engineering physics , catalysis , electrode , chemistry , organic chemistry , electrolyte , physics , quantum mechanics , machine learning , computer science , engineering
The hole-injection and recombination photophysics for NiO sensitized with RuP ([Ru II (bpy) 2 (4,4'-(PO 3 H 2 ) 2 -bpy)] 2+ ) are explored. Ultrafast transient absorption (TA) measurements performed with an external electrochemical bias reveal the efficiency for productive hole-injection, that is, quenching of the dye excited state that results in a detectable charge-separated electron-hole pair, is linearly dependent on the electronic occupation of intragap states in the NiO film. Population of these states via a negative applied potential increases the efficiency from 0% to 100%. The results indicate the primary loss mechanism for dye-sensitized NiO is rapid nongeminate recombination enabled by the presence of latent holes in the surface of the NiO film. Our findings suggest a new design paradigm for NiO photocathodes and devices centered on the avoidance of this recombination pathway.

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