TY - JOUR
T1 - Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design
AU - Passarelli, James V.
AU - Fairfield, Daniel J.
AU - Sather, Nicholas A.
AU - Hendricks, Mark P.
AU - Sai, Hiroaki
AU - Stern, Charlotte L.
AU - Stupp, Samuel I.
N1 - Funding Information:
This work was primarily supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, under award no. DE-FG02-00ER45810. Work on single-crystal conductivity measurements was supported by the Air Force Research Laboratory under agreement number FA8650-15-2-5518. N.A.S. was supported by the Department of Defense (DoD), Air Force Office of Scientific Research, through the National Defense Science and Engineering Graduate (NDSEG) Fellowship, 32 CFR 168a. N.A.S. and J.V.P. also acknowledge support from Northwestern University through a Ryan Fellowship. We would like to thank Michelle Chen for photoluminescence measurements. This work made use of the IMSERC at Northwestern University, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205); the State of Illinois and International Institute for Nanotechnology (IIN). This work made use of the EPIC, Keck-II, and SPID facilities of Northwestern University’s NUANCE Center, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205); the MRSEC program (DMR-1720139) at the Materials Research Center; the International Institute for Nanotechnology (IIN); the Keck Foundation; and the State of Illinois, through the IIN. This work made use of the J. B. Cohen X-ray Diffraction Facility supported by the MRSEC program of the National Science Foundation (DMR-1720139) at the Materials Research Center of Northwestern University [LCP1]. This work made use of the Northwestern University Micro/Nano Fabrication Facility (NUFAB), which is partially supported by Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205), the Materials Research Science and Engineering Center (NSF DMR-1720139), the State of Illinois, and Northwestern University. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357.
Funding Information:
This work was primarily supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, under award no. DE- FG02-00ER45810. Work on single-crystal conductivity measurements was supported by the Air Force Research Laboratory under agreement number FA8650-15-2-5518. N.A.S. was supported by the Department of Defense (DoD), Air Force Office of Scientific Research, through the National Defense Science and Engineering Graduate (NDSEG) Fellowship 32 CFR 168a. N.A.S. and J.V.P. also acknowledge support from Northwestern University through a Ryan Fellowship. We would like to thank Michelle Chen for photoluminescence measurements. This work made use of the IMSERC at Northwestern University, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205); the State of Illinois and International Institute for Nanotechnology (IIN).
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/6/13
Y1 - 2018/6/13
N2 - Layered perovskites with the formula (R-NH3)2PbI4 have excellent environmental stability but poor photovoltaic function due to the preferential orientation of the semiconducting layer parallel to the substrate and the typically insulating nature of the R-NH3 + cation. Here, we report a series of these n = 1 layered perovskites with the form (aromatic-O-linker-NH3)2PbI4 where the aromatic moiety is naphthalene, pyrene, or perylene and the linker is ethyl, propyl, or butyl. These materials achieve enhanced conductivity perpendicular to the inorganic layers due to better energy level matching between the inorganic layers and organic galleries. The enhanced conductivity and visible absorption of these materials led to a champion power conversion efficiency of 1.38%, which is the highest value reported for any n = 1 layered perovskite, and it is an order of magnitude higher efficiency than any other n = 1 layered perovskite oriented with layers parallel to the substrate. These findings demonstrate the importance of leveraging the electronic character of the organic cation to improve optoelectronic properties and thus the photovoltaic performance of these chemically stable low n layered perovskites.
AB - Layered perovskites with the formula (R-NH3)2PbI4 have excellent environmental stability but poor photovoltaic function due to the preferential orientation of the semiconducting layer parallel to the substrate and the typically insulating nature of the R-NH3 + cation. Here, we report a series of these n = 1 layered perovskites with the form (aromatic-O-linker-NH3)2PbI4 where the aromatic moiety is naphthalene, pyrene, or perylene and the linker is ethyl, propyl, or butyl. These materials achieve enhanced conductivity perpendicular to the inorganic layers due to better energy level matching between the inorganic layers and organic galleries. The enhanced conductivity and visible absorption of these materials led to a champion power conversion efficiency of 1.38%, which is the highest value reported for any n = 1 layered perovskite, and it is an order of magnitude higher efficiency than any other n = 1 layered perovskite oriented with layers parallel to the substrate. These findings demonstrate the importance of leveraging the electronic character of the organic cation to improve optoelectronic properties and thus the photovoltaic performance of these chemically stable low n layered perovskites.
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U2 - 10.1021/jacs.8b03659
DO - 10.1021/jacs.8b03659
M3 - Article
C2 - 29869499
AN - SCOPUS:85048744184
SN - 0002-7863
VL - 140
SP - 7313
EP - 7323
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 23
ER -