“Using light and colors to unravel the invisible of interfaces”
Passionate about my work, this website enables me to present my research as well as communicating on my work, what I do, why I do it, and explaining my research tools such as the synchrotron.
“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.
A Unified Framework for Electrochemical interfaces
The inherent complexity of interfaces has historically forced a fragmentation of scientific understanding: physics governed the solid, molecular chemistry addressed the surface, and electrochemistry managed the electrolyte. My recent work, published in Nature Communications, seeks 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 attemps 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!
Next to come
2026 MRS Spring Meeting & Exhibit
This Spring, I will be attending the 2026 MRS Spring Meeting & Exhibit in Honolulu, Hawai‘i. I am deeply honored to have been invited to present our work at the symposium on Nanodiamonds.
My presentation, titled "Probing, Understanding, and Engineering Diamond Interfaces for Quantum and Energy Technologies," will provide a comprehensive review of the techniques used to investigate diamond surfaces and nanodiamonds. Specifically, I will discuss how we probe surface states and defects using NEXAFS, depth-resolved XPS, and STXM. Furthermore, I will explore the interactions between these surfaces and their environment, and the resulting implications for future technologies.
Picture highlight
Diamonds are not just precious stones—they can also be grown in the lab and engineered into advanced materials for science and technology. In this image, taken with an electron microscope, you can see "diamond black" electrodes developed by my collaborator, Dr. Peter Knittel from the Fraunhofer Institute. These electrodes feature a surface covered with needle-like structures, designed to significantly increase the contact area with water, enhancing their efficiency in chemical reactions. This innovation highlights the incredible potential of diamond-based materials in cutting-edge research.
Last Publication
Recycling CO₂ with Electrons from Nanodiamonds
Kiendl, B., Chemin, A., Day, A. H., Rodriguez, R. B., Choudhury, S., Buchner, F., ... & Krueger, A. (2026). Intrabandgap States Engineering in Functionalized Nanodiamond to Generate Solvated Electrons for Photocatalysis Under Solar Illumination. Advanced Functional Materials, e23545.
In close collaboration with Tristan Petit from Helmholtz-Zentrum Berlin and Anke Krueger from Stuttgart, we have published an article entitled “Intrabandgap States Engineering in Functionalized Nanodiamond to Generate Solvated Electrons for Photocatalysis Under Solar Illumination” in the journal Advanced Functional Materials.
Diamond can emit solvated electrons, extremely powerful reducing agents capable of transforming CO₂. However, it normally operates only under deep ultraviolet light, which is scarcely present in sunlight. By modifying the surface of nanodiamonds, we introduced electronic states within their bandgap, enabling them to absorb visible light.
More importantly, we show that electron generation under solar illumination does not depend solely on the material itself, but on a subtle balance of charges between the nanodiamond, its surface states, and the surrounding water.
This work lays the foundations for solar catalysis based on controlling interfaces at the nanoscale and mastering electronic equilibria between solids and liquids.