High Efficiency Quantum Dot Heterojunction Solar Cell Using Anatase (001) TiO2 Nanosheets
High Efficiency Quantum Dot Heterojunction Solar Cell Using Anatase (001) TiO2 Nanosheets
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DOI:
10.1002/adma.201104497
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发表时间:
2012-04-24
影响因子:
29.4
通讯作者:
Graetzel, Michael
中科院分区:
文献类型:
--
作者:
Etgar, Lioz;Zhang, Wei;Graetzel, Michael
Quantum dots (QDs) have attracted a lot of attention due to their tunable bandgap and their high optical absorption cross section.[1–3] A variety of research projects attempt to integrate QDs into solar cells devices, including nanocrystal (NC)-poly mer hybrid solar cells, NC-Schottky solar cells, NC-sensitized titanium dioxide (TiO 2) solar cells, and NC hybrid bilayer solar cells.[4–12] Recently investigations focus on QD heterojunction solar cells, by placing oxide NCs (TiO 2 or ZnO) as a thin spacer layer between the QDs and the FTO.[13–19] In addition, a tandem QD solar cell with the same structure has been demonstrated as well.[20] Multiple exciton generation (MEG) effect was also demonstrate in similar QD based solar cell structure.[21]PbS and PbSe QDs belong to group IV-VI, which are known for their high absorbance in the visible and in the near infrared regions. They have a relatively large Bohr radius,[22–24] large ground state cross section of absorption (∼ 10–15 cm− 2) and long excitonic lifetime (∼ 200–800 ns).[25] In addition their bandgap can be tuned between 0.3–2.0 eV The crystal structure of anatase TiO 2 can be theoretically constructed as truncated octahedron with eight equivalent (101) facets and two equivalent (001) facets on the top/bottom.[26] Studies have shown that the (001) facets of anatase TiO 2 are more reactive than the (101) facets which are more thermodynamically stable.[27] Moreover, the band edge of anatase TiO 2 with dominant (101) facets is more negative than the exposed (001) anatase TiO 2.[28]