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

Citation data:

Journal of Materials Chemistry A, ISSN: 2050-7496, Vol: 6, Issue: 10, Page: 4305-4312

Publication Year:
2018
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Repository URL:
http://scholarworks.unist.ac.kr/handle/201301/23823
DOI:
10.1039/c7ta09504j
Author(s):
Javaid, Saqib; Myung, Chang Woo; Yun, Jeonghun; Lee, Geunsik; Kim, Kwang S.
Publisher(s):
Royal Society of Chemistry (RSC); The Royal Society of Chemistry; ROYAL SOC CHEMISTRY
Tags:
Chemistry; Energy; Materials Science
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article description
Methylammonium lead-iodide (MAPbI, MA: CH-NH) interfaced with rutile TiOis widely used in photovoltaic devices. These devices utilize the electron transfer from MAPbIto TiO, 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 TiO/MAPbIsystem. 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 TiOsubstrate, highlighting orientationally ordered MA at the interface. The optimized interface structure shows the C-N axis of MA titled towards the TiOsurface 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 TiOhas a critical impact on the energy level alignment at the interface, thus driving the electron transfer process from MA to TiO. 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.