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Increased resistance to photooxidation in Dion-Jacobson lead halide perovskites -- implication for perovskite device stability
Authors:
Zhilin Ren,
Juraj Ovčar,
Tik Lun Leung,
Yanling He,
Yin Li,
Dongyang Li,
Xinshun Qin,
Hongbo Mo,
Zhengtian Yuan,
Jueming Bing,
Martin P. Bucknall,
Luca Grisanti,
Muhammad Umair Ali,
Peng Bai,
Tao Zhu,
Ali Ashger Syed,
Jingyang Lin,
Jingbo Wang,
Abdul-Khaleed,
Wenting Sun,
Gangyue Li,
Gang Li,
Alan Man Ching Ng,
Anita W. Y. Ho-Baillie,
Ivor Lončarić
, et al. (2 additional authors not shown)
Abstract:
2D metal halide perovskites have enabled significant stability improvements in perovskite devices, particularly in resistance to moisture. However, some 2D perovskites are even more susceptible to photooxidation compared to 3D perovskites. This is particularly true for more commonly investigated Ruddlesden-Popper (RP) perovskites that exhibit increased susceptibility to photoinduced degradation co…
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2D metal halide perovskites have enabled significant stability improvements in perovskite devices, particularly in resistance to moisture. However, some 2D perovskites are even more susceptible to photooxidation compared to 3D perovskites. This is particularly true for more commonly investigated Ruddlesden-Popper (RP) perovskites that exhibit increased susceptibility to photoinduced degradation compared to Dion-Jacobson (DJ) perovskites. Comparisons between different RP and DJ perovskites reveal that this phenomenon cannot be explained by commonly proposed differences in superoxide ion generation, interlayer distance and lattice structural rigidity differences. Instead, the resistance to photooxidation of DJ perovskites can be attributed to decreased likelihood of double deprotonation events (compared to single deprotonation events in RP perovskites) required for the loss of organic cations and the perovskite decomposition. Consequently, DJ perovskites are less susceptible to oxidative degradation (both photo- and electrochemically induced), which leads to improved operational stability of solar cells based on these materials.
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Submitted 19 September, 2024;
originally announced September 2024.
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Quantitative reconstruction of defects in multi-layered bonded composites using fully convolutional network-based ultrasonic inversion
Authors:
Jing Rao,
Fangshu Yang,
Huadong Mo,
Stefan Kollmannsberger,
Ernst Rank
Abstract:
Ultrasonic methods have great potential applications to detect and characterize defects in multi-layered bonded composites. However, it remains challenging to quantitatively reconstruct defects, such as disbonds and kissing bonds, that influence the integrity of adhesive bonds and seriously reduce the strength of assemblies. In this work, an ultrasonic method based on the supervised fully convolut…
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Ultrasonic methods have great potential applications to detect and characterize defects in multi-layered bonded composites. However, it remains challenging to quantitatively reconstruct defects, such as disbonds and kissing bonds, that influence the integrity of adhesive bonds and seriously reduce the strength of assemblies. In this work, an ultrasonic method based on the supervised fully convolutional network (FCN) is proposed to quantitatively reconstruct defects hidden in multi-layered bonded composites. In the training process of this method, an FCN establishes a non-linear mapping from measured ultrasonic data to the corresponding velocity models of multi-layered bonded composites. In the predicting process, the trained network obtained from the training process is used to directly reconstruct the velocity models from the new measured ultrasonic data of adhesively bonded composites. The presented FCN-based inversion method can automatically extract useful features in multi-layered composites. Although this method is computationally expensive in the training process, the prediction itself in the online phase takes only seconds. The numerical results show that the FCN-based ultrasonic inversion method is capable to accurately reconstruct ultrasonic velocity models of the high contrast defects, which has great potential for online detection of adhesively bonded composites.
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Submitted 11 September, 2021;
originally announced September 2021.
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Magnetic structure of the field-induced multiferroic GdFe3(BO3)4
Authors:
Haiding Mo,
Christie S. Nelson,
Leonard N. Bezmaternykh,
V. T. Temerov
Abstract:
We report a magnetic x-ray scattering study of the field-induced multiferroic GdFe3(BO3)4. Resonant x-ray magnetic scattering at the Gd LII,III edges indicates that the Gd moments order at TN ~ 37 K. The magnetic structure is incommensurate below TN, with the incommensurability decreasing monotonically with decreasing temperature until a transition to a commensurate magnetic phase is observed at…
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We report a magnetic x-ray scattering study of the field-induced multiferroic GdFe3(BO3)4. Resonant x-ray magnetic scattering at the Gd LII,III edges indicates that the Gd moments order at TN ~ 37 K. The magnetic structure is incommensurate below TN, with the incommensurability decreasing monotonically with decreasing temperature until a transition to a commensurate magnetic phase is observed at T ~ 10 K. Both the Gd and Fe moments undergo a spin reorientation transition at TSR ~ 9 K such that the moments are oriented along the crystallographic c axis at low temperatures. With magnetic field applied along the a axis, our measurements suggest that the field-induced polarization phase has a commensurate magnetic structure with Gd moments rotated ~45 degrees toward the basal plane, which is similar to the magnetic structure of the Gd subsystem observed in zero field between 9 and 10 K, and the Fe subsystem has a ferromagnetic component in the basal plane.
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Submitted 20 November, 2008;
originally announced November 2008.
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Spin-charge-lattice coupling near the metal-insulator transition in Ca3Ru2O7
Authors:
C. S. Nelson,
H. Mo,
B. Bohnenbuck,
J. Strempfer,
N. Kikugawa,
S. I. Ikeda,
Y. Yoshida
Abstract:
We report x-ray scattering studies of the c-axis lattice parameter in Ca3Ru2O7 as a function of temperature and magnetic field. These structural studies complement published transport and magnetization data, and therefore elucidate the spin-charge-lattice coupling near the metal-insulator transition. Strong anisotropy of the structural change for field applied along orthogonal in-plane direction…
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We report x-ray scattering studies of the c-axis lattice parameter in Ca3Ru2O7 as a function of temperature and magnetic field. These structural studies complement published transport and magnetization data, and therefore elucidate the spin-charge-lattice coupling near the metal-insulator transition. Strong anisotropy of the structural change for field applied along orthogonal in-plane directions is observed. Competition between a spin-polarized phase that does not couple to the lattice, and an antiferromagnetic metallic phase, which does, gives rise to rich behavior for B $\parallel$ b.
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Submitted 5 June, 2007;
originally announced June 2007.
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Nanoscale Observation of Alkane Delayering
Authors:
M. Bai,
K. Knorr,
M. J. Simpson,
S. Trogisch,
H. Taub,
S. N. Ehrlich,
H. Mo,
U. G. Volkmann,
F. Y. Hansen
Abstract:
Noncontact Atomic Force Microscopy and synchrotron x-ray scattering measurements on dotriacontane (n-C32H66 or C32) films adsorbed on SiO2-coated Si(100) wafers reveal a narrow temperature range near the bulk C32 melting point Tb in which a monolayer phase of C32 molecules oriented perpendicular to surface is stable. This monolayer phase undergoes a delayering transition to a three-dimensional (…
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Noncontact Atomic Force Microscopy and synchrotron x-ray scattering measurements on dotriacontane (n-C32H66 or C32) films adsorbed on SiO2-coated Si(100) wafers reveal a narrow temperature range near the bulk C32 melting point Tb in which a monolayer phase of C32 molecules oriented perpendicular to surface is stable. This monolayer phase undergoes a delayering transition to a three-dimensional (3D) fluid phase on heating to just above Tb and to a solid 3D phase on cooling below Tb. An equilibrium phase diagram provides a useful framework for interpreting the unusual spreading and receding of the monolayer observed in transitions to and from the respective 3D phases.
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Submitted 18 November, 2006;
originally announced November 2006.
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Conformational rearrangements in thin films of polydimethylsiloxane melt
Authors:
Guennadi Evmenenko,
Haiding Mo,
Sumit Kewalramani,
Pulak Dutta
Abstract:
Synchrotron X-ray reflectivity (XRR) confirms the formation of a quasi-immobilized layer in thin films of polydimethylsiloxane (PDMS) melts near silica surfaces. This layer (40-60A) has a lower density than the bulk value, and its thickness varies slightly with PDMS molecular weight. Formation of this layer is very rapid for PDMS melts with low molecular weights (below entanglement limit for the…
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Synchrotron X-ray reflectivity (XRR) confirms the formation of a quasi-immobilized layer in thin films of polydimethylsiloxane (PDMS) melts near silica surfaces. This layer (40-60A) has a lower density than the bulk value, and its thickness varies slightly with PDMS molecular weight. Formation of this layer is very rapid for PDMS melts with low molecular weights (below entanglement limit for these molecules) but takes 5-10 hours for higher molecular weights (close to and above their entanglement value).
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Submitted 26 October, 2005;
originally announced October 2005.
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Observation of surface layering in a nonmetallic liquid
Authors:
Haiding Mo,
Guennadi Evmenenko,
Sumit Kewalramani,
Kyungil Kim,
Steven N. Ehrlich,
Pulak Dutta
Abstract:
Oscillatory density profiles (layers) have previously been observed at the free surfaces of liquid metals, but not in other isotropic liquids. We have used x-ray reflectivity to study a molecular liquid, tetrakis(2-ethylhexoxy)silane. When cooled to T/Tc~0.25 (well above the freezing point for this liquid), density oscillations appear at the surface. Lateral order within the layers is liquid-lik…
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Oscillatory density profiles (layers) have previously been observed at the free surfaces of liquid metals, but not in other isotropic liquids. We have used x-ray reflectivity to study a molecular liquid, tetrakis(2-ethylhexoxy)silane. When cooled to T/Tc~0.25 (well above the freezing point for this liquid), density oscillations appear at the surface. Lateral order within the layers is liquid-like. Our results confirm theoretical predictions that a surface-layered state will appear even in dielectric liquids at sufficiently low temperatures, if not preempted by freezing.
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Submitted 17 February, 2006; v1 submitted 26 October, 2005;
originally announced October 2005.