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Alberto García-Fernández

Publications and source records attributed to Alberto García-Fernández.

2 recordsLinked to original sources

Resolving the energy alignment between methylammonium lead iodide and C60: an in-situ photoelectron spectroscopy study

Understanding and controlling the energy level alignment at interfaces between lead halide perovskites and electron transport layers is crucial for optimizing perovskite-based devices such as solar cells. In this work, we investigated the energy level alignment of C60 on in-situ cleaved MAPbI3 single crystals in multiple repeat experiments using photoelectron spectroscopy aiming to resolve inconsistencies reported in earlier studies. Our results show that both materials remain chemically stable upon interface formation, in contrast to the strong reactions typically seen when metals are evaporated on perovskite surfaces. By analyzing the Pb 4f and C 1s binding energies in detail, we determined that C60 consistently exhibits a downward energy shift toward MAPbI3, which works against efficient charge extraction. The magnitude of this shift, however, varies between different sample positions, highlighting that small variations in sample surfaces can lead to significant differences in energetic alignment. At higher C60 coverages of more than 5 monolayers, a constant HOMO-valence band offset of 0.52 eV was obtained. These findings underscore the decisive role of surface chemistry on interfacial energetics, explain performance variability in perovskite devices, and demonstrate the need to control and accurately measure surface properties. Furthermore, the observed energetic alignment can explain why further interface modification by charge blocking layers or surface passivation is needed for optimized device efficiencies.

cond-mat.mtrl-sci↗

Strong Electron-Phonon Coupling and Lattice Dynamics in One-Dimensional [(CH3)2NH2]PbI3 Hybrid Perovskite

Hybrid halide perovskites (HHPs) have attracted significant attention due to their remarkable optoelectronic properties that combine the advantages of low cost-effective fabrication methods of organic-inorganic materials. Notably, low-dimensional hybrid halide perovskites including two-dimensional (2D) layers and one-dimensional (1D) chains, are recognized for their superior stability and moisture resistance, making them highly appealing for practical applications. Particularly, DMAPbI3 has attracted attention due to other interesting behaviors and properties, such as thermally induced order-disorder processes, dielectric transition, and cooperative electric ordering of DMA dipole moments. In this paper, we investigated the interplay between low-temperature SPT undergone by the low-dimensional (1D) hybrid halide perovskite-like material DMAPbI3 and its optoelectronic properties. Our approach combines synchrotron X-ray powder diffraction, Raman spectroscopy, thermo-microscopy, differential scanning calorimetry (DSC), and photoluminescence (PL) techniques. Temperature-dependent Synchrotron powder diffraction and Raman Spectroscopy reveal that the modes associated with I-Pb-I and DMA+ ion play a crucial role in the order-disorder SPT in DMAPbI3. The reversible SPT modifies its optoelectronic properties, notably affecting its thermochromic behavior and PL emission. The origin of the PL phenomenon is associated to self-trapped excitons (STEs), which are allowed due to a strong electron-phonon coupling quantified by the Huang-Rhys factor (S = 97+-1). Notably, we identify the longitudinal optical (LO) phonon mode at 84 cm-1 which plays a significant role in electron-phonon interaction. Our results show these STEs not only intensify the PL spectra at lower temperatures but also induce a shift in the color emission, transforming it from a light orange-red to an intense bright strong red.

cond-mat.mtrl-sci↗