Toggle Main Menu Toggle Search

Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Can aliphatic anchoring groups be utilised with dyes for p-type dye sensitized solar cells?

Lookup NU author(s): Chris Wood, Professor Elizabeth GibsonORCiD

Downloads


Licence

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).


Abstract

A series of novel laterally anchoring tetrahydroquinoline derivatives have been synthesized and investigated for their use in NiO-based p-type dye-sensitized solar cells. The kinetics of charge injection and recombination at the NiO-dye interface for these dyes have been thoroughly investigated using pico-second transient absorption and time-resolved infrared measurements. It was revealed that despite the anchoring unit being electronically decoupled from the dye structure, charge injection occurred on a sub pico-second timescale. However, rapid recombination was also observed due to the close proximity of the electron acceptor on the dyes to the NiO surface, ultimately limiting the performance of the p-DSCs.


Publication metadata

Author(s): Hao H, Wood CJ, Clark CA, Calladine J, Horvath R, Hanson-Heine M, Sun XZ, Clark IP, Towrie M, George MW, Yang X, Sun L, Gibson EA

Publication type: Article

Publication status: Published

Journal: Dalton Transactions

Year: 2016

Volume: 45

Issue: 18

Pages: 7708-7719

Print publication date: 14/05/2016

Online publication date: 29/03/2016

Acceptance date: 29/03/2016

Date deposited: 08/04/2016

ISSN (print): 1477-9226

ISSN (electronic): 1477-9234

Publisher: Royal Society of Chemistry

URL: http://dx.doi.org/10.1039/C6DT00146G

DOI: 10.1039/C6DT00146G


Altmetrics

Altmetrics provided by Altmetric


Share