Description

PRISM programme

 The PRISM (PhD Research Programme for International Training in Sustainable Soft Matter) programme has launched its first call for applications, offering up to 14 fully funded PhD fellowships starting from 1 March 2027 at Paris Sciences & Lettres (PSL) University. The programme trains researchers to address ecological transition challenges through sustainable soft matter science, with projects focused on eco-friendly chemical processes, circular economy, renewable energies, and carbon capture, storage, and valorisation. Co-funded by the European Union under Horizon Europe MSCA COFUND (Grant Agreement 101261637) and partner institutions, PRISM provides interdisciplinary, international, and intersectoral training, including mobility opportunities, secondments, and courses in sustainability, innovation, entrepreneurship, career development, and transferable skills.

 Applications must be submitted via the PRISM website (https://prism.psl.eu/en/) by 31 October 2026 (23:59 Paris time).

 

The PhD project

 The transition toward sustainable energy systems critically relies on the development of efficient water electrolysis technologies for green hydrogen production. However, the performance of electrolyzers is strongly limited by the formation, growth, and adhesion of gas bubbles at electrode surfaces, which block active sites, increase local resistance, and alter mass transport near the interface. Despite extensive studies, the fundamental mechanisms governing the earliest stages of bubble nucleation, occurring at the nanometric scale, remain poorly understood due to the lack of suitable in situ characterization techniques.

 This PhD proposal aims to address this major knowledge gap by developing an innovative experimental approach combining electrochemical control with in situ Atomic Force Microscopy (AFM) in liquid environments. Building on recent advances and the installation of a new electrochemical AFM platform within the ESPCI premises, the project will provide unprecedented access to molecular-scale processes occurring at electrode/electrolyte interfaces during water electrolysis. In particular, it seeks to elucidate the transition from solvent restructuring under applied potential to gas supersaturation and ultimately nanobubble nucleation.

 The scientific rationale rests on the hypothesis that bubble nucleation is a metastable process governed by a subtle interplay between local surface properties (chemistry, wettability, roughness, defects) and electrochemical conditions. To get novel fundamental insights into this process, we will first focus on model electrodes (e.g., graphite). We will rely on high-speed and high-resolution dynamic force spectroscopy of near-surface structural and solvation forces, which will provide insight into the early stages of bubble nucleation — from solvent restructuring under electrochemical potential, to interfacial gas saturation, to bubble nucleation and growth kinetics. We will then extend our investigations towards more realistic electrodes, using high-resolution imaging of surface nanobubbles to correlate local bubble nucleation with surface chemistry (hydrophilicity/hydrophobicity balance), topography, and defects. Together, these measurements will help identify nucleation pathways and clarify the role of surface heterogeneities in triggering bubble formation.

 A second objective will then be to establish quantitative correlations between these nanoscale observations and macroscopic electrochemical performance. By systematically varying electrode materials and surface treatments, we will aim to determine how local interfacial phenomena influence global efficiency, thereby providing guidelines for the rational design of improved electrodes with reduced bubble-related losses.

 Overall, this PhD project is highly innovative in its ability to access previously inaccessible interfacial phenomena at the nanoscale and to bridge the gap between interfacial soft matter, solid/liquid interfaces, fundamental surface science and applied electrochemical engineering. Its expected outcomes will contribute to both fundamental understanding and technological advances in hydrogen production, positioning it at the forefront of research on energy-related interfacial processes.

 

3i dimensions

 INTERNATIONAL: The project has a strong international dimension through established and planned collaborations with leading experts in interfacial science and advanced AFM, providing complementary expertise in confined electrolyte studies under surface-force apparatus, molecular-scale characterization of solid–liquid interfaces, and interfacial liquid structuring. The compulsory international secondment (minimum one month) will ideally take place at one of these partner laboratories, enabling knowledge transfer, access to complementary instrumentation, and strengthening the international impact and visibility of the project.

 INTERSECTORAL: The project has a strong intersectoral potential through its direct relevance to industrial challenges in hydrogen production and surface engineering. A collaboration or secondment with an industrial partner such as TotalEnergies or Saint-Gobain will be sought to investigate the role of engineered surface coatings and functional interfaces on gas bubble nucleation, growth and detachment during water electrolysis.

 INTERDISCIPLINARY: The project is highly interdisciplinary, bridging together concepts in interfacial physics, soft matter, electrochemistry, surface science and electrocatalysis. It combines advanced scanning probe microscopy, molecular-scale characterization of solid–liquid interfaces, electrochemical measurements and materials engineering to investigate gas bubble nucleation during water electrolysis. By linking nanoscale interfacial phenomena to macroscopic electrochemical performance, the project integrates fundamental physics and physical chemistry with challenges in energy conversion and materials design.

 

Eligibility criteria

1. At the time of application, candidates must be in possession of their Master’s degree or equivalent/postgraduate degree which formally entitles them to start a doctorate. All applicants with a doctoral degree are ineligible.
2. A minimum English proficiency level of C1 (Advanced) is required for applicants from non-English-speaking countries. No French language skills are required.
3. Applicants must fulfil the transnational mobility rule: open to all nationalities but all incoming applicants must not have resided or carried out their main activity (work, studies, etc.) in France for more than 12 months in the 3 years immediately prior to the call for applications deadline.
4. Applicants must be available to start the program on schedule: 1st March 2027.
5. Completeness of the application, submitted in English on the PRISM dedicated website, before the deadline of 31 October 2026.

 

*Name of the school of PSL*

ESPCI - PSL (Ecole Supérieure de Physique et de Chimie Industrielles de la ville de Paris)

 

Research Unit

Soft Matter Science and Engineering (UMR 7615, SIMM)

Institute of Porous MAterials of Paris (UMR 8004, IMAP)

 The project team brings together complementary expertise from two researchers, J. Comtet and L. Assaud, based in two ESPCI research units: the Soft Matter Science and Engineering Laboratory (SIMM) and the Institute of Porous Materials of Paris (IMAP). J. Comtet's research focuses on probing the transport and dynamics of soft matter at interfaces, at the nano- and molecular scale, using innovative experimental approaches ranging from scanning probe to single-molecule imaging. L. Assaud's work centers on the characterization and optimization of novel two-dimensional electrochemical interfaces and electrocatalytic processes through nanostructuration. This project is thus unique in bringing together complementary expertise in electrochemistry (IMAP), wetting and solid/liquid interfaces (SIMM), and quantitative scanning probe microscopy (IMAP, SIMM). By combining in situ electrochemical AFM with systematic surface engineering to directly observe the nucleation and early growth of gas bubbles at the nanoscale, this approach will enable the exploration of interfacial material properties at the nanometric scales, and open new avenues for the design of highly efficient electrodes for water electrolysis.

 

Supervision

Supervisor: jean.comtet@espci.fr

Co-supervisor: loic.assaud@espci.fr

 Candidates are encouraged to contact the project supervisors to discuss the proposed research topics before applying. All projects are open PhD projects, meaning that the research plan will be further developed collaboratively by the selected doctoral candidate and the supervisors.

Skills required

We are looking for a master's student with a background in physics, materials science, electrochemistry, or physical chemistry, who is excited to dive into an interdisciplinary project at the crossroads of soft matter, interfacial physics and physico-chemistry, liquid-state physics, electrochemistry, and electrocatalysis. The envisioned AFM experiments are technically demanding and require great care and precision: a strong aptitude for hands-on experimental work with complex, custom-built instruments — here, Atomic Force Microscopy — together with solid data analysis skills, will be key to making the most of this project. Beyond technical background, we are above all looking for someone curious, open-minded, and able to think independently, who is eager to take ownership of a research question at the frontier of physics and electrochemistry.

Bibliography

References [1] Kempler, P. A., Coridan, R. H., & Luo, L. (2024). Gas evolution in water electrolysis. Chemical reviews, 124(19), 10964-11007. [2] Zhang, L., Zhang, Y., Zhang, X., Li, Z., Shen, G., Ye, M., ... & Hu, J. (2006). Electrochemically controlled formation and growth of hydrogen nanobubbles. Langmuir, 22(19), 8109-8113. [3] Utsunomiya, T., Yokota, Y., Enoki, T., & Fukui, K. I. (2014). Potential-dependent hydration structures at aqueous solution/graphite interfaces by electrochemical frequency modulation atomic force microscopy. Chemical Communications, 50(98), 15537-15540. [4] Martin-Jimenez, D., Chacon, E., Tarazona, P., & Garcia, R. (2016). Atomically resolved threedimensional structures of electrolyte aqueous solutions near a solid surface. Nature communications, 7(1), 12164. [5] Comtet, Jean, et al. "Nanoscale capillary freezing of ionic liquids confined between metallic interfaces and the role of electronic screening." Nature materials 16.6 (2017): 634-639.

Keywords

Solid/liquid interfaces, nanobubbles, nanofluidics, electrocatalysis, energy, hydrogen, Atomic Force Microscopy