Articles and Theses – 2024

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Articles

Peeters, W. H. J.; Vettori, M.; Fadaly, E. M. T.; Danescu, A.; Mao, C.; Verheijen, M. A.; Bakkers, E. P. A. M.

Onset of Uncontrolled Polytypism during the Au-Catalyzed Growth of Wurtzite GaAs Nanowires

Phys. Rev. Mater. 2024, 8 (2), L020401

Shani, L.; Lueb, P.; Menning, G.; Gupta, M.; Riggert, C.; Littmann, T.; Hackbarth, F.; Rossi, M.; Jung, J.; Badawy, G.; Verheijen, M. A.; Crowell, P. A.; Bakkers, E. P. A. M.; Pribiag, V. S.

Diffusive and Ballistic Transport in Thin InSb Nanowire Devices Using a Few-Layer-Graphene-AlOx Gate

Mater. Quantum. Technol. 2024, 4 (1), 015101.

https://doi.org/10.1088/2633-4356/ad2d6b

Melian A.R. Blijlevens, Ekaterina D. Garina, Quirine D.K. Wildeman, Roy van Alst, Natalia Mazur, Hugo`Meekes and Elias Vlieg,

NaI as suitable alkali halide hydrate for domestic thermochemical heat storage

Journal of Energy Storage, 88 (2024) 111651, 1-12.

https://doi.org/10.1016/j.est.2024.111651.

Runhua Wang, Zhengshuo Zhan, Bingnan Song, Michel Saakes, Renata D. van der Weijden, Cees J.N. Buisman, Yang Lei,

Electrochemical route outperforms chemical struvite precipitation in mitigating heavy metal contamination

Journal of Hazardous Materials, 465, 2024, 133418, ISSN 0304-3894

https://doi.org/10.1016/j.jhazmat.2023.133418

M. H. Bistervels, A. van der Weijden, H. Schoenmaker, M. Kamp, W. L. Noorduin

Compose and Convert: Controlling Shape and Chemical Composition of Self-Organizing Nanocomposites

Adv. Funct. Mater. 2024, 2403715.

https://doi.org/10.1002/adfm.202403715

Le Dizès Castell, R.; Mirzahossein, E.; Grzelka, M.; Jabbari-Farouji, S.; Bonn, D.; Shahidzadeh, N.

Visualization of the Sol–Gel Transition in Porous Networks Using Fluorescent Viscosity-Sensitive Probes

J. Phys. Chem. Lett. 2024, 15 (2), 628–635

https://doi.org/10.1021/acs.jpclett.3c02634.

Vries, T. E. de; Vlieg, E.; Gelder, R. de.

Unravelling the Structure of the CSD Cocrystal Network Using a Fast Near-Optimal Bipartisation Algorithm for Large Networks

CrystEngComm 2024, 26 (2), 192–202.

https://doi.org/10.1039/D3CE00978E

Gerard, C. J. J.; Pinetre, C.; Cercel, H.; Charpentier, M. D.; Sanselme, M.; Couvrat, N.; Brandel, C.; Cartigny, Y.; Dupray, V.; ter Horst, J. H.

Phase Diagrams of Praziquantel and Vanillic Acid Cocrystals: Racemic Compound and Conglomerate System.

Crystal Growth & Design 2024.

https://doi.org/10.1021/acs.cgd.4c00114.

Nagaraj Nagalingam, Vikram Korede, Daniel Irimia, Jerry Westerweel, Johan T. Padding, Remco Hartkamp & Hüseyin Burak Eral

Unified framework for laser-induced transient bubble dynamics within microchannels

Sci Rep 14, 18763 (2024)

https://doi.org/10.1038/s41598-024-68971-x

Vries, Tom E. de; Eert, Evi van; Weevers, Lucas; Tinnemans, P.T.; Vlieg, E.; Meekes, H.L.M.; Gelder, R. de,

Optimizing Link Prediction for the CSD Cocrystal Network: A Demonstration Using Praziquantel

Crystal Growth & Design, 2024, 24(12), 5200-5210

https://doi.org/10.1021/acs.cgd.4c00438

Pinetre, Clement; Ritou, Loic; Gerard, Charline J.J.; Cercel, Hugo; Leeman, M.; Kellogg, R.M.; Tinnemans, P.T.; Dupray, Valerie; Horst, J.H. ter.

Rare Case of Polymorphism in the Binary System of Enantiomers of a Praziquantel Derivative

Organic Process Research & Development, 2024, 28(4), 1224-1232

https://doi.org/10.1021/acs.oprd.4c00035

Krabben, L.M. van der; Gruginskie, N.; Eerden, Maarten van; Gastel, Jasper van; Mulder, Peter; Bauhuis, G.J.; Khusyainov, Dinar; Afanasiev, D.; Vlieg, Elias; Schermer, J.J.,

Reduced Surface Recombination in Extended-Perimeter LEDs toward Electroluminescent Cooling

ACS Applied Electronic Materials, 2024, 6(2), 1483-1492

https://doi.org/10.1021/acsaelm.3c01816

Mattinen, M., Chen, W., Dawley, R. A., Verheijen, M. A., Hensen, E. J. M., Kessels, W. M. M. & Bol, A. A.

Structural Aspects of MoSx Prepared by Atomic Layer Deposition for Hydrogen Evolution Reaction

ACS Catalysis. 14(13) (2024) 10089-10101

https://doi.org/10.1021/acscatal.4c01445

Rossi, M., van Schijndel, T. A. J., Lueb, P., Badawy, G., Jung, J., Peeters, W. H. J., Kölling, S., Moutanabbir, O., Verheijen, M. A. & Bakkers, E. P. A. M.

Stemless InSb nanowire networks and nanoflakes grown on InP

Nanotechnology 35(41) (2024) 415602

https://iopscience.iop.org/article/10.1088/1361-6528/ad61ef

Peeters, W. H. J., van Lange, V. T., Belabbes, A., van Hemert, M. C., Jansen, M. M., Farina, R., van Tilburg, M. A. J., Verheijen, M. A., Botti, S., Bechstedt, F., Haverkort, J. E. M. & Bakkers, E. P. A. M. ,

Direct bandgap quantum wells in hexagonal Silicon Germanium

Nature Communications 15(1) (2024) 5252

https://doi.org/10.1038/s41467-024-49399-3

Mientjes, M. G. C., Guan, X. , Lueb, P. J. H., Verheijen, M. A. & Bakkers, E. P. A. M.

Catalyst-free MBE growth of PbSnTe nanowires with tunable aspect ratio

Nanotechnology 35(32) (2024) 325602

https://iopscience.iop.org/article/10.1088/1361-6528/ad47c8

Rovaris, F., Peeters, W. H. J., Marzegalli, A., Glas, F., Vincent, L., Miglio, L., Bakkers, E. P. A. M., Verheijen, M. A. & Scalise

2H-Si/Ge for Group-IV Photonics: on the Origin of Extended Defects in Core-Shell Nanowires

ACS Applied Nano Materials. 7(8) (2024) 9396–9402

https://doi.org/10.1021/acsanm.4c00835

F. Valls Mascaró, M.T.M. Koper, and M.J. Rost

Step Bunching Instability and its Effects in Electrocatalysis: Pt(111) and its Vicinal Surfaces

Nature Catalysis, (2024)

https://doi.org/10.1038/s41929-024-01232-2

F. Valls Mascaró, M.T.M. Koper, and M.J. Rost

Quantitative Study of Electrochemical Adsorption and Oxidation on Pt(111) and its Vicinal Surfaces

Electrochim. Acta, 506, 145014 (2024)

https://doi.org/10.1016/j.electacta.2024.145014

Theses

Marco Rossi

Epitaxy of Bottom-Up Grown InSb Nanostructures
PhD defense: 23 mei 2024, Eindhoven University of Technology, Eindhoven
Promoter: prof. dr. Erik Bakkers
Co-promoter: dr. Marcel A. Verheijen

Quantum computers are a revolutionary computing paradigm based on quantum mechanics. They use qubits, the quantum equivalent of bits, to potentially solve problems that classical computers cannot. Preserving the delicate quantum state of qubits is a challenge due to decoherence caused by interactions with the environment. Topological quantum computation offers a promising solution by utilizing Majorana zero modes (MZMs), which are quasiparticles excitations that are resistant to local sources of decoherence. This inherent robustness makes MZMs highly desirable for quantum information processing. Despite various theoretical proposals outlined the necessary conditions for achieving MZMs, experimental realization has yet to be achieved, leaving the existence of MZMs as an open question. The primary impediment to detecting MZMs currently stems from the level of disorder (e.g. crystal defects, impurities, surface roughness) present in the semiconductor-superconductor hybrid devices required for testing their existence. Furthermore, providing definitive proof necessitates the fabrication of a material platform wherein MZMs can be intricately braided within a complex network. These challenges require concerted material science efforts to provide such platform with minimal disorder. This thesis focuses on the bottom-up epitaxy of free-standing nanostructures made of indium antimonide (InSb), a promising semiconductor for constructing such devices due to its unique physical properties.

Marloes Bistervels

Light-controlled self-assembly | Crystallization in the spotlight

PhD defense: 29 November 2024, University of Amsterdam

Promotor: Prof. dr. Wim Noorduin
Co-promotor: Prof. dr. Fred Brouwer

Precise control over biotic and abiotic self-assembly processes is of fundamental interest, with practical implications for developing simple and scalable routes toward complex three-dimensional (3D) architectures with advanced functionalities. While techniques for achieving either local and static or dynamic and global control have been developed, local and dynamic control remains challenging. In this thesis, we harness light to achieve spatiotemporal control over the self-assembly of biorelevant crystals.
By utilizing photochemical reactions, we create local gradients of precursors that drive the nucleation and growth of bioinspired co-precipitation of barium carbonate nanocrystals and amorphous silica. Using a custom-built optical setup and optimizing the UV irradiation with the reaction conditions, we control self-assembly in terms of time, position, nucleation rate, and morphology.
By employing near-infrared (NIR) laser light, we demonstrate spatiotemporal control over the crystallization of retrograde soluble compounds induced by locally heating water. Modulating the NIR light intensity enables to start, steer, and stop crystallization of carbonate minerals with micrometer precision. By integrating ion exchange into the light-driven self-assembly process, we introduce a two-step strategy based on self-organization and conversion reactions, shaping a diverse range of chemical compositions into user-defined designs. Considering thermodynamic stability and chemical reactivity, we design orthogonal conversion reactions for the sequential positioning of different metal chalcogenide semiconductors and the integration of various compositions into the same hybrid architecture. This work opens previously unimaginable opportunities for light-directed self-assembly of functional composites, forging a genuine collaboration with self-assembly processes: simple hands-off autonomy when possible, and precise hands-on command when necessary.
https://dare.uva.nl/search?identifier=bc9d1913-8abf-47a9-b25e-6a7a38a4a3b5

Eline Grothe

Classification of Stereoisomerism and Multicomponent Systems in Crystallographic Databases

PhD defense: 1 November 2024, Radboud Universiteit, Nijmegen

Promotor: Prof. dr. Elias Vlieg
Co-promotors: Dr. Hugo Meekes, Dr. R. de Gelder

The magnitude and growing complexity of the data in crystallographic databases such as the Cambridge Structural Database (CSD) can pose a challenge when assembling the right data set to address a research question. This is complicated further by the limitations of available search possibilities and the complexity of problem statements. This thesis describes the development
of methods that are needed to assemble a dataset based on chirality of the components and based on the composition of multicomponent crystals.
https://repository.ubn.ru.nl/handle/2066/311641

Nagaraj Nagalingam

Laser-Induced Cavitation for Controlling Crystallization from Solution

PhD defense: 14 October 2024, Delft University of Technology
Promotor: Dr. H.B. Eral, Prof. dr. J.T. Padding

Primary nucleation control is crucial for obtaining crystals with specific properties, such as purity, size, morphology, and polymorphic form. Non-photochemical laser-induced nucleation (NPLIN) has attracted interest due to its ability to control these properties without chemical reactions, using non-invasive methods, and allowing spatio-temporal precision. However, the exact
mechanism underlying NPLIN remains debated in the literature. This dissertation explores how micron-sized vapor bubbles, formed by laser interaction with supersaturated aqueous solutions, can trigger crystal nucleation. Despite aqueous solutions
generally being transparent to laser wavelengths of 532 nm and 1064 nm, transient bubbles can still form due to energy absorption by impurities or by focusing the laser. The research begins by examining the crystallization of KCl in aqueous solutions, initiated by bubbles formed using focused laser light with nanosecond pulse width. Findings show that solute accumulation at the bubble surface exceeds the saturation limit, leading to localized supersaturation. A finite element method model, validated by experimental bubble size data, is used to estimate solute transfer and supersaturation levels. The model demonstrates a concentrated solute boundary layer around the bubble, driven by high solvent evaporation rates associated with bubble growth. The experimental results for crystallization probability and crystal count align with classical nucleation theory predictions based on the numerically estimated supersaturation at the vapor-liquid interface. The bubble formation mechanism proposed for NPLIN is extended to other solutes like NH4Cl, NaCl, KBr, and CH4N2O. Experiments with NH4Cl and NaCl yield a general analytical relation for supersaturation in the liquid surrounding the bubble, explaining NPLIN activity for these solutes when an unfocused laser is used. The predicted bubble sizes, based on Mie theory, correlate with the minimum nucleation rate necessary for crystal formation, indicating that the bubble-driven mechanism is a key factor in NPLIN. Since isolated bubbles are rare in irradiated volumes due to the random distribution of impurities, the study also investigates bubble-bubble interactions and their effect on crystallization. The dynamics of single laser-induced bubbles in microchannel geometries are analyzed, revealing a unified theory for bubble size and lifetime as a function of laser energy. This analysis also uncovers a transient flow instability, rare in low Reynolds number flows, which originates from the channel walls and is characterized by the Womersley number and flow timescale. The research further demonstrates crystallization using bubble pairs in microchannels with KMnO4 as a model salt. The interaction between bubbles produces microjets that alter nucleation kinetics through induced shear, enabling crystallization at lower laser energies and
solution supersaturation compared to single bubbles. A numerical model based on the boundary integral element method is used to predict microjet velocities and the resulting shear, correlating these factors with crystallization probabilities. Overall, this work advances understanding of NPLIN, suggesting that bubble formation and interactions can be harnessed to achieve targeted crystallization with lower energy inputs and reduced supersaturation, paving the way for more efficient laser-induced crystallization
processes.

https://repository.tudelft.nl/record/uuid:17b93f25-8f3f-4ab4-b5f8-ba446d923b6d

Vikram B. Korede

Taming Crystallization with Light

PhD defense: 7 October 2024, Delft University of Technology
Promotor: Dr. H.B. Eral, Prof. dr. J.T. Padding

Crystallization is one of the most widely used purification and separation processes applied in a multitude of industries such as pharmaceuticals, food & beverages, agriculture, and fine chemicals. However, the initial step of the crystallization process, nucleation, is still poorly understood and highly stochastic. As a result, most crystallization processes lack proper control
over the properties of the crystals produced. Among many techniques for achieving better control over the nucleation process, the application of non-photochemical laser induced nucleation (NPLIN) has gathered significant interest. This is because of its potential to improve product quality in crystallization processes by directly controlling the nucleation rate, both spatially and temporally. Additionally, NPLIN can induce crystallization in solutions that would otherwise take a long time to nucleate, offering a unique advantage over traditional methods. However, despite its promising capabilities, NPLIN is not widely used in practice yet. The
fundamental mechanism behind NPLIN is not fully understood, making it unclear how it should be applied effectively in practice and for which systems NPLIN could be beneficial. This Ph.D. project aims to delve into the fundamental mechanisms of NPLIN, by examining how specific laser and solution parameters influence nucleation kinetics, leveraging innovative experimental setups. Laser parameters being studied include laser-exposed volume, laser irradiation position, laser intensity and laser wavelength, and solution parameters include supersaturation levels, solution filtration, and the presence of impurities or dopants, particularly nanoparticles. The thesis begins with a comprehensive review of the experimental and computational literature on NPLIN. It then presents a detailed study on the effect of the laser-exposed volume and laser irradiation position on the nucleation probability within partly illuminated supersaturated aqueous potassium chloride solutions. An increase in the laser-exposed volume resulted in a higher nucleation probability and a higher number of crystals per nucleated sample. Furthermore, laser irradiation, particularly through the air/solution interface, not only enhances nucleation probability but also influences the formation of different crystal morphologies. These observations are partly explained by the Nanoparticle Heating mechanism and the Dielectric Polarization model (Chapter 2). The research then transitions to a microfluidic platform, which allows for high-throughput and crystallization detection using the deep learning method. This innovative approach addresses the need for large data sets in NPLIN research, which has been a significant challenge due to the manual nature of traditional experiments. The study examines the effects of laser intensity, wavelength, supersaturation, solution filtration, and intentional doping on nucleation probability in supersaturated potassium chloride solutions. Higher laser intensities and increased supersaturation significantly enhance nucleation probabilities. The laser wavelength effect was only observed for 355 nm at higher laser intensities. Solution filtration suppresses the NPLIN effect, whereas the addition of nanoparticles as dopants into the solution not only increases the NPLIN probabilities but also affects the crystal morphology. The results highlight the importance of impurities in the solution and support the hypothesis that
nanoparticle or impurity heating could be the key mechanism in understanding NPLIN (Chapter 3). The study finally investigated the effects of solution filtration, laser intensity, and nanoparticle properties including nanoparticle concentration and material on NPLIN probability in supersaturated aqueous urea solutions. The study highlights the significant role of impurities in NPLIN, demonstrating that doping with different nanoparticle materials leads to varied nucleation probabilities. In particular, gold nanoparticles were found to enhance nucleation more effectively than silica nanoparticles. Additionally, it was observed that NPLIN probabilities followed a Poisson distribution to changes in nanoparticle concentration and laser intensity respectively. The findings in this chapter enhance our understanding of the critical role of impurities in comprehending the NPLIN mechanism (Chapter 4).
https://repository.tudelft.nl/record/uuid:7c197383-2adc-49d6-9b28-cfd93114142b

Francesc Valls Mascaro

Platinum Surface Instabilities and their Impact in Electrochemistry

PhD defense: 5 September 2024, Leiden University
Promotors: Prof. dr. M. T. M. Koper, Dr. M. J. Rost

Hydrogen fuel cells are expected to be pivotal for the energy transition towards renewable energy sources. However, their economic feasibility is severely hindered by the high cost and degradation rate of the platinum electrode, which forms the key component for the catalytic reaction. Addressing this challenge necessitates designing improved catalysts, which requires a better fundamental understanding of both their reactivity and their degradation mechanism. In this thesis, we investigate the stability of model platinum surfaces submerged in electrolyte under an applied voltage, thus simulating the operational conditions of fuel cells. For this we used a home-build Electrochemical Scanning Tunneling Microscope (EC-STM), which allows us to observe the surface structure at the atomic scale in real time during its operation. Our findings surprisingly show that several instabilities lead to significant structural changes. At high voltages, nanoislands with dendritic shapes form during the reduction of the surface oxide, which is the origin of the surface roughening and thus linked to the catalyst degradation. Moreover, we demonstrate that closely-spaced atomic steps are unstable and bunch together, resulting in steps with multi-atomic heights. This structural change has a significant effect on the catalyst reactivity as well as on its potential of zero charge, as we explain in detail. Finally, we investigate
vicinal platinum surfaces to better understand the reactivity of facets on nanoparticles: again we find an instability leading to structural changes. Overall, this thesis sheds light on the fundamental, atomic processes that drive platinum surface restructuring as well as their implications for reactivity.
https://scholarlypublications.universiteitleiden.nl/handle/1887/4054933

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