Enabling Efficient Creation of Long-Lived Charge-Separation on Dye-Sensitized NiO Photocathodes

被引:43
作者
Dillon, Robert J. [1 ]
Alibabaei, Leila [1 ]
Meyer, Thomas J. [1 ]
Papanikolas, John M. [1 ]
机构
[1] Univ North Carolina Chapel Hill, Dept Chem, Chapel Hill, NC 27514 USA
关键词
hole-injection; recombination; dye-sensitized nickel oxide NiO; transient absorption; applied bias; solar fuels; photocathode; DENSITY-OF-STATES; ELECTRON INJECTION; POLYPYRIDYL DYES; HOLE INJECTION; REDOX COUPLE; METAL-OXIDES; SOLAR-CELLS; COMPLEXES; DYNAMICS; FILMS;
D O I
10.1021/acsami.7b05856
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The hole-injection and recombination photophysics for NiO sensitized with RuP ([Ru-II(bpy)(2)(4,4'-(PO3H2)(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.
引用
收藏
页码:26786 / 26796
页数:11
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