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Lee, Geunsik
Electronic Structure and Transport in Condensed Materials
Research Interests
  • open quantum system, non-equilibrium electron transport

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Organic cation steered interfacial electron transfer within organic-inorganic perovskite solar cells

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Title
Organic cation steered interfacial electron transfer within organic-inorganic perovskite solar cells
Author
Javaid, SaqibMyung, Chang WooYun, JeonghunLee, GeunsikKim, Kwang S.
Issue Date
201803
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.6, no.10, pp.4305 - 4312
Abstract
Methylammonium lead-iodide (MAPbI3, MA: CH3–NH3) interfaced with rutile TiO2 is widely used in photovoltaic devices. These devices utilize the electron transfer from MAPbI3 to TiO2, which may not be explained solely by the band structures of the two bulk materials. To elucidate the interface dynamics and its impact on the electron transfer process, we have studied the interfacial features of a TiO2/MAPbI3 system. First principles calculations and ab initio molecular dynamics simulations show that the rotational freedom of MA present within the bulk is considerably suppressed due to interaction of MA with the TiO2 substrate, highlighting orientationally ordered MA at the interface. The optimized interface structure shows the C–N axis of MA titled towards the TiO2 surface so as to maximize the interaction between N-attached H and underlying O. The very short O⋯H⋯N distance with very large hydrogen bonding energy identifies short strong hydrogen bonding (SSHB) as the origin of structural re-organization at the interface. As for the electronic structure, this proton sharing between MA and TiO2 has a critical impact on the energy level alignment at the interface, thus driving the electron transfer process from MA to TiO2. Indeed, significant reduction in the electron transfer barrier is observed for the energetically optimal interface configuration which promotes the electron transfer across the interface and photovoltaic properties.
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DOI
http://dx.doi.org/10.1039/C7TA09504J
ISSN
2050-7488
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