TY - JOUR
T1 - Enhanced charge transport and photovoltaic performance induced by incorporating rare-earth phosphor into organic-inorganic hybrid solar cells
AU - Chen, Zihan
AU - Li, Qinghua
AU - Chen, Chuyang
AU - Du, Jiaxing
AU - Tong, Jifeng
AU - Jin, Xiao
AU - Li, Yue
AU - Yuan, Yongbiao
AU - Qin, Yuancheng
AU - Wei, Taihuei
AU - Sun, Weifu
PY - 2014/10/21
Y1 - 2014/10/21
N2 - In this work, dysprosium ion decorated yttrium oxide (Dy3+:Y2O3) nanocrystal phosphors were incorporated into TiO2 acceptor thin film in a bid to enhance the light harvest, charge separation and transfer in the hybrid solar cells. The results show that the energy level offset between the donor (P3HT) and the acceptor (Dy3+:Y2O3-TiO2) has been narrowed down, thus leading to the enhanced electron and hole transports, and also photovoltaic performances as compared to pure TiO2 without incorporating Dy3+:Y2O3. By applying femtosecond transient optical spectroscopy, after the incorporation of dopant Dy3+:Y2O3 into TiO2 at 6 wt%, both the hot electron and hole transfer lifetimes have been shortened, that is, from 30.2 ps and 6.94 ns to 25.1 ps and 1.26 ns, respectively, and an enhanced efficiency approaching 3% was achieved as compared to 2.0% without doping, indicating that the energetic charges are captured more efficiently benefitting a higher power conversion efficiency. Moreover, these results reveal that both the conduction band (CB) and valence band (VB) edges of the acceptor were elevated by 0.57 and 0.32 eV, respectively, after incorporating 6 wt% Dy3+:Y2O3. This work demonstrates that distinct energy level alignment engineered by Dy3+:Y2O3 phosphor has an important role in pursuing efficient future solar cells and underscores the promising potential of rare-earth phosphor in solar applications.
AB - In this work, dysprosium ion decorated yttrium oxide (Dy3+:Y2O3) nanocrystal phosphors were incorporated into TiO2 acceptor thin film in a bid to enhance the light harvest, charge separation and transfer in the hybrid solar cells. The results show that the energy level offset between the donor (P3HT) and the acceptor (Dy3+:Y2O3-TiO2) has been narrowed down, thus leading to the enhanced electron and hole transports, and also photovoltaic performances as compared to pure TiO2 without incorporating Dy3+:Y2O3. By applying femtosecond transient optical spectroscopy, after the incorporation of dopant Dy3+:Y2O3 into TiO2 at 6 wt%, both the hot electron and hole transfer lifetimes have been shortened, that is, from 30.2 ps and 6.94 ns to 25.1 ps and 1.26 ns, respectively, and an enhanced efficiency approaching 3% was achieved as compared to 2.0% without doping, indicating that the energetic charges are captured more efficiently benefitting a higher power conversion efficiency. Moreover, these results reveal that both the conduction band (CB) and valence band (VB) edges of the acceptor were elevated by 0.57 and 0.32 eV, respectively, after incorporating 6 wt% Dy3+:Y2O3. This work demonstrates that distinct energy level alignment engineered by Dy3+:Y2O3 phosphor has an important role in pursuing efficient future solar cells and underscores the promising potential of rare-earth phosphor in solar applications.
UR - http://www.scopus.com/inward/record.url?scp=84908125706&partnerID=8YFLogxK
U2 - 10.1039/c4cp03232b
DO - 10.1039/c4cp03232b
M3 - Article
AN - SCOPUS:84908125706
SN - 1463-9076
VL - 16
SP - 24499
EP - 24508
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 44
ER -