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Coexistence of Two Electronic Nano-Phases on a CH3NH3PbI3–xClx Surface Observed in STM Measurements
Author(s) -
Andrew J. Yost,
Artem Pimachev,
ChunChih Ho,
Seth B. Darling,
Leeyih Wang,
WeiFang Su,
Yuri Dahnovsky,
TeYu Chien
Publication year - 2016
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.6b07721
Subject(s) - materials science , perovskite (structure) , dipole , electronic structure , scanning tunneling microscope , spectral line , ferroelectricity , condensed matter physics , phase (matter) , density functional theory , molecular physics , analytical chemistry (journal) , crystallography , nanotechnology , physics , computational chemistry , chemistry , dielectric , optoelectronics , chromatography , quantum mechanics , astronomy
Scanning tunneling microscopy is utilized to investigate the local density of states of a CH 3 NH 3 PbI 3-x Cl x perovskite in cross-sectional geometry. Two electronic phases, 10-20 nm in size, with different electronic properties inside the CH 3 NH 3 PbI 3-x Cl x perovskite layer are observed by the dI/dV mapping and point spectra. A power law dependence of the dI/dV point spectra is revealed. In addition, the distinct electronic phases are found to have preferential orientations close to the normal direction of the film surface. Density functional theory calculations indicate that the observed electronic phases are associated with local deviation of I/Cl ratio, rather than different orientations of the electric dipole moments in the ferroelectric phases. By comparing the calculated results with experimental data we conclude that phase A (lower contrast in dI/dV mapping at -2.0 V bias) contains a lower I/Cl ratio than that in phase B (higher contrast in dI/dV).

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