My research lives at the interface — literally: the few nanometres where a solid electrode meets a liquid, and where reactions are won or lost. Working on diamond surfaces and (photo)electrochemistry, I combine synchrotron X-ray spectroscopy with lab characterization and the theory to tie it together — chasing one unified picture of interfacial charge transfer rather than a catalogue of special cases.
“God made the bulk, surfaces were invented by the devil.”
Wolfgang Pauli
In the interior of a material, atoms exist in a state of predictable, repeating symmetry. But at the surface, that order vanishes. Atoms are left with "dangling bonds," creating a restless environment where materials rearrange, react, and succumb to even the slightest contamination. This inherent instability is what makes surfaces notoriously difficult to model and control, yet so profoundly interesting to investigate.
This "devilish" complexity is exactly where modern technology lives. Whether it is the flow of electrons in a sub-nanometer transistor, the exchange of ions at a battery electrode, the precise chemical signaling of a biosensor, or the electrochemical production of biofuels—the most critical physical processes do not happen within the volume of a material; they happen at the interface.
My research is dedicated to navigating this frontier. By understanding, probing, and engineering these atomic boundaries, I work to transform the unpredictable chaos of the surface into a foundation for more efficient electronics and sustainable energy solutions.
Understanding the Hidden Electrical Barrier at Solid–Liquid Interfaces
The inherent complexity of interfaces has historically forced a fragmentation of scientific understanding. We are essentially speaking two different languages, physicists describe how electrons behave inside the solid, while chemists focus on the molecular reactions in the liquid. But electrochemistry happens precisely where those two meet. I seek to bridge these silos by introducing a unified theoretical formalism. It integrates four fundamental pillars:
Solid State Physics: To describe Fermi levels, band structures, and doping effects within the solid bulk.
Molecular Chemistry: To account for electron affinities and surface reactivity, grounded in the Sabatier principle.
Chemical Thermodynamics: To model redox potentials and the critical influence of pH within the electrolyte.
Electrostatics & Transport Dynamics: To couple reaction kinetics with Helmholtz double layers and depletion zones.
By merging these disciplines, I demonstrate that the origin of the Helmholtz electric double layer lies in the equilibrium of charges at the interface, dictated by the chemical potential of electrons in both the solid and the liquid. This equilibrium creates a significant electric potential variation (so called Helmholtz potential) and local electric fields, which have a direct impact on interfacial electrochemistry.
This framework provides a theoretical basis for emerging concepts—such as the entropy of the electrolyte at the interface—which are becoming critical descriptors of electrocatalytic activity. By incorporating this electronic equilibrium directly into the Butler-Volmer formalism, we can finally account for the decisive role of the Helmholtz potential in governing reaction kinetics.
Ultimately, this approach attempts to transform the "devilish" unpredictability of the interface into a predictable, engineered landscape, providing the missing link for truly understanding and mastering electrochemical systems.
Recycling CO₂: At the Heart of Future Physical Chemistry
A truly sustainable energy transition will only be possible by closing the carbon cycle by recycling CO2 and using it as a raw material for the organic chemistry of tomorrow (pharmaceuticals, fuels, plastics, etc.). To achieve this, our research aims to understand and optimize the (photo)electrocatalysis of CO2 and the production of H2, utilizing the direct conversion of electrical and solar energy into chemical energy.
Materials Innovation: We develop new generations of electrodes inspired by photovoltaics (thin films, rare-earth-doped semiconductors) and innovative materials such as synthetic diamonds, MXene or high-entropy alloys nanoparticles.
Understanding Interfaces: We develop new theoretical approaches to decrypt the complexity of solid–liquid interfaces and overcome bottlenecks related to catalytic kinetics and reaction selectivity.
Multi-scale Characterization: Our work relies on laboratory techniques and advanced synchrotron methods for structural, electronic, and chemical characterization.
Are you curious about combining fundamental research with environmental challenges? Come discover our projects at the laboratory!