arXiv subjects

Ernest Pastor

Publications and source records attributed to Ernest Pastor.

10 recordsLinked to original sources

arXiv2026

Spin-lattice coupling enables adaptive adsorption in magnetically-driven electrocatalysts

A major challenge in electrochemistry is to decouple the reactive intermediates of a catalytic cycle to optimise their energies independently. During the oxygen evolution reaction (OER), such energy interdependence results from the need to generate multiple adsorbates at the same site and sets the minimum overpotential. Here, we show that an external stimulus, such as a magnetic field, can relax the scaling relationships between intermediates during the OER. Spectroscopic measurements and Density Functional Theory simulations in Ni-Fe oxyhydroxides reveal that applying a magnetic field alters surface chemisorption and injects structural flexibility at the interface. We interpret these observations as a consequence of stimulated changes in the spin-lattice coupling, which allow access to quasi-degenerate oxygenated intermediates that modulate the reaction energy demands. Our findings redefine the scaling limitations as state-projected rather than intrinsic and establish external stimulation as a strategy to navigate multi-state energy landscapes in electrocatalysis and sensing applications.

cond-mat.mtrl-sci↗

arXiv2026

Thermodynamics of the ultrafast phase transition of vanadium dioxide

Ultrafast photoexcitation is an emerging route to selective control of phase transitions. However, it is difficult to determine which modes govern the transformation and how effectively they are targeted by photoexcitation. This is exemplified in vanadium dioxide, which transitions from a monoclinic insulator to a rutile metal upon heating or photoexcitation. There is a long-standing debate about whether this transition is electronically or structurally driven and whether the structural component is coherent, driven by a single structural mode or thermal in nature. In this work, we develop a simple thermodynamic framework based on temperature-dependent ultrafast pump-probe measurements and contrast it to microscopic-detail-free modelling to identify the driving mechanism of the transition, revealing that population of the full thermal phonon spectrum, especially high-frequency oxygen modes, is necessary to stabilize the metallic phase. Our approach can straightforwardly be applied to determine the nature of other photoinduced phase transitions without the need for complex multi-messenger experiments and can guide new control strategies, even for incoherent transitions.

cond-mat.str-el↗

arXiv2024

Ultrafast lattice disordering can be accelerated by electronic collisional forces

In the prevalent picture of ultrafast structural phase transitions, the atomic motion occurs in a slowly varying potential energy surface determined adiabatically by the fast electrons. However, this ignores non-conservative forces caused by electron-lattice collisions, which can significantly influence atomic motion. Most ultrafast techniques only probe the average structure and are less sensitive to random displacements, and therefore do not detect the role played by non-conservative forces in phase transitions. Here we show that the lattice dynamics of the prototypical insulator-to-metal transition of VO2 cannot be described by a potential energy alone. We use the sample temperature to control the preexisting lattice disorder before ultrafast photoexcitation across the phase transition and our ultrafast diffuse scattering experiments show that the fluctuations characteristic of the rutile metal develop equally fast (120 fs) at initial temperatures of 100 K and 300 K. This indicates that additional non-conservative forces are responsible for the increased lattice disorder. These results highlight the need for more sophisticated descriptions of ultrafast phenomena beyond the Born-Oppenheimer approximation as well as ultrafast probes of spatial fluctuations beyond the average unit cell measured by diffraction.

cond-mat.str-el↗

arXiv2023

Dynamics of electronic states in the insulating Intermediate surface phase of 1T-TaS$_2$

This article reports a comparative study of bulk and surface properties in the transition metal dichalcogenide 1T-TaS$_2$. When heating the sample, the surface displays an intermediate insulating phase that persists for $\sim 10$ K on top of a metallic bulk. The weaker screening of Coulomb repulsion and stiffer Charge Density Wave (CDW) explain such resilience of a correlated insulator in the topmost layers. Both time resolved ARPES and transient reflectivity are employed to investigate the dynamics of electrons and CDW collective motion. It follows that the amplitude mode is always stiffer at the surface and displays variable coupling to the Mott-Peierls band, stronger in the low temperature phase and weaker in the intermediate one.

cond-mat.str-el↗

arXiv2023

All-optical seeding of a light-induced phase transition with correlated disorder

Ultrafast manipulation of vibrational coherence is an emergent route to control the structure of solids. However, this strategy can only induce long-range correlations and cannot modify atomic structure locally, which is required in many technologically-relevant phase transitions. Here, we demonstrate that ultrafast lasers can generate incoherent structural fluctuations which are more efficient for material control than coherent vibrations, extending optical control to a wider range of materials. We observe that local, non-equilibrium lattice distortions generated by a weak laser pulse reduce the energy barrier to switch between insulating and metallic states in vanadium dioxide by 6%. Seeding inhomogeneous structural-fluctuations presents an alternative, more energy efficient, route for controlling materials that may be applicable to all solids, including those used in data and energy storage devices.

cond-mat.str-el↗

arXiv2023

Correlating activity and defects in (photo)electrocatalysts using in-situ transient optical microscopy

(Photo)electrocatalysts capture sunlight and use it to drive chemical reactions such as water splitting to produce H2. A major factor limiting photocatalyst development is their large heterogeneity which spatially modulates reactivity and precludes establishing robust structure-function relationships. To make such links requires simultaneously probing of the electrochemical environment at microscopic length scales (nm to um) and broad timescales (ns to s). Here, we address this challenge by developing and applying in-situ steady-state and transient optical microscopies to directly map and correlate local electrochemical activity with hole lifetimes, oxygen vacancy concentration and the photoelectrodes crystal structure. Using this combined approach alongside spatially resolved X-Ray absorption measurements, we study microstructural and point defects in prototypical hematite (Fe2O3) photoanodes. We demonstrate that regions of Fe2O3, adjacent to microstructural cracks have a better photoelectrochemical response and reduced back electron recombination due to an optimal oxide vacancy concentration, with the film thickness and carbon impurities also dramatically influencing activity in a complex manner. Our work highlights the importance of microscopic mapping to understand activity and the impact of defects in even, seemingly, homogeneous solid-state metal oxide photoelectrodes.

physics.chem-ph↗

arXiv2023

Electronic dispersion, correlations and stacking in the photoexcited state of 1T-TaS$_2$

Here we perform angle and time-resolved photoelectron spectroscopy on the commensurate Charge Density Wave (CDW) phase of 1T-TaS$_2$. Data with different probe pulse polarization are employed to map the dispersion of electronic states below and above the chemical potential. Upon photoexcitation, the fluctuations of CDW order erase the band dispersion near to the chemical potential and halve the charge gap size. This transient phase sets within half a period of the coherent lattice motion and is favored by strong electronic correlations. The experimental results are compared to Density-Functional Theory (DFT) calculations with a self-consistent evaluation of the Coulomb repulsion. Our simulations indicate that the screening of Coulomb repulsion depends on the stacking order of the TaS$_2$ layers. The entanglement of such degrees of freedom suggest that both the structural order and electronic repulsion are locally modified by the photoinduced CDW fluctuations.

cond-mat.str-el↗

arXiv2022

Electronic Defects in Metal Oxide Photocatalysts

A deep understanding of defects is essential for the optimisation of materials for solar energy conversion. This is particularly true for metal oxide photo(electro)catalysts, which typically feature high concentrations of charged point defects that are electronically active. In photovoltaic materials, except for selected dopants, defects are considered detrimental and should be eliminated to minimise charge recombination. However, photocatalysis is a more complex process where defects can play an active role, for example, by stabilising charge separation and mediating rate-limiting catalytic steps. Here, we review the behaviour of electronic defects in metal oxides, paying special attention to the principles underpinning the formation and function of trapped charges in the form of polarons. We focus on how defects alter the electronic structure, statically or transiently upon illumination, and discuss the implications of such changes in light-driven catalytic reactions. Finally, we consider the applicability of lessons learned from oxide defect chemistry to new photocatalysts based on carbon nitrides, polymers and metal halide perovskites.

cond-mat.mtrl-sci↗

arXiv2022

Non-thermal breaking of magnetic order via photo-generated spin defects

In Mott insulators the evolution of antiferromagnetic order to superconducting or charge-density-wave-like states upon chemical doping underpins the control of quantum phases. Photo-doping can induce similar transitions on the ultrafast timescale, however the response of the spin system has remained elusive. Here, we use 4D-ultrafast optical spectroscopy to extract quantitative magnetic dynamics in the spin-orbit coupled Mott insulator Sr3Ir2O7. We demonstrate that light can non-thermally melt long-range spin order. At low fluences magnetic order recovers within 1 ps despite demagnetization of roughly 50%. However, high fluences induce a crossover to a long-lived demagnetized state without increasing the lattice temperature. We show that the generation of photo-induced spin defects enables a mechanism that stabilizes the demagnetized state which could help expose new transient phases.

cond-mat.str-el↗

arXiv2021

All-Chalcogenide Programmable All-Optical Deep Neural Networks

Deeplearning algorithms are revolutionising many aspects of modern life. Typically, they are implemented in CMOS-based hardware with severely limited memory access times and inefficient data-routing. All-optical neural networks without any electro-optic conversions could alleviate these shortcomings. However, an all-optical nonlinear activation function, which is a vital building block for optical neural networks, needs to be developed efficiently on-chip. Here, we introduce and demonstrate both optical synapse weighting and all-optical nonlinear thresholding using two different effects in a chalcogenide material photonic platform. We show how the structural phase transitions in a wide-bandgap phase-change material enables storing the neural network weights via non-volatile photonic memory, whilst resonant bond destabilisation is used as a nonlinear activation threshold without changing the material. These two different transitions within chalcogenides enable programmable neural networks with near-zero static power consumption once trained, in addition to picosecond delays performing inference tasks not limited by wire charging that limit electrical circuits; for instance, we show that nanosecond-order weight programming and near-instantaneous weight updates enable accurate inference tasks within 20 picoseconds in a 3-layer all-optical neural network. Optical neural networks that bypass electro-optic conversion altogether hold promise for network-edge machine learning applications where decision-making in real-time are critical, such as for autonomous vehicles or navigation systems such as signal pre-processing of LIDAR systems.

physics.optics↗