Searcharxiv⌕ Search
Home/Archive/arXiv

arXiv · 2006.15362

Probing dynamics of water mass transfer in organic porous photocatalyst water-splitting materials by neutron spectroscopy

Mohamed Zbiri·Catherine M. Aitchison·Reiner S. Sprick·Andrew I. Cooper·Anne A. Y. Guilbert
View original source ↗Read source document ↗Export metadata ↓

Abstract

The quest for efficient and economically accessible cleaner methods to develop sustainable carbon-free energy sources induced a keen interest in the production of hydrogen fuel. This can be achieved via the water-splitting process exploiting solar energy but requiring the use of adequate photocatalysts. Covalent triazine-based frameworks (CTFs) are target photocatalysts for water-splitting. Both electronic and structural characteristics of CTFs, optical bandgaps and porosity, are directly relevant for water-splitting. These can be engineered through chemical design. Porosity can be beneficial to water-splitting by providing larger surface area for the catalytic reactions. However, porosity can also affect both charge transport within the photocatalyst and mass transfer of both reactants and products, thus impacting the overall kinetics of the reaction. We focus on the link between chemical design and water (reactants) mass transfer, playing a key role in the water uptake process and the subsequent hydrogen generation. We use neutron spectroscopy to study water mass transfer in two porous CTFs, CTF-CN and CTF-2, that differ in the polarity of their struts. Quasi-elastic neutron scattering (QENS) is used to quantify the amount of bound water and the translational diffusion of water. Inelastic neutron scattering measurements complement QENS and provides insights into the softness of the CTF structures and the changes in librational degrees of freedom of water in CTFs. We show that CTF-CN exhibits smaller surface area and water uptake due to a softer structure than CTF-2. The current study leads to new insights into the structure-dynamics-property relationship of CTF photo-catalysts that pave the road for a better understanding of the guest-host interaction at the basis of water splitting applications.

Explore related subjects

cond-mat.mtrl-scicond-mat.soft

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Mohamed Zbiri, Catherine M. Aitchison, Reiner S. Sprick, Andrew I. Cooper, Anne A. Y. Guilbert. 2021-02-23. Probing dynamics of water mass transfer in organic porous photocatalyst water-splitting materials by neutron spectroscopy. https://doi.org/10.1021/acs.chemmater.0c04425

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

arXiv2026

Measuring chiral phonons

Chiral phonons are quantized vibrations where the atomic motion in a solid breaks improper rotation symmetries. In many cases, chiral phonons possess angular momenta and are therefore selective to circularly polarized light. Both fundamental and applied research efforts on chiral phonons have been gaining increasing attention owing to their importance in a variety of fields including spintronics, spin-selective chemical reactions, thermal transport, quantum information processing and biosensing, where the bi-directional spin-lattice coupling enabled by chiral phonons can be harnessed in new ways, and potentially lead to new functionalities. Thus far, the studies of chiral phonons across diverse materials platforms have evolved largely independently within these fields, but the experimental techniques are often interrelated. In this perspective, we present a detailed description, as well as advantages and disadvantages of the current approaches for experimentally measuring chiral phonons in chiral and achiral materials. We conclude with a discussion of new methods for measuring chiral phonons. Ultimately, this work seeks to offer an experimental guide for systematically investigating the properties of chiral phonons in various materials systems and applications.

cond-mat.mtrl-sci↗
arXiv2026

A model of grain growth in UN integrating molecular dynamics, phase-field modeling, and uncertainty quantification

Grain growth kinetics and grain-boundary (GB) properties in uranium mononitride (UN) are investigated through an integrated multiscale framework combining molecular dynamics (MD), phase-field modeling, and surrogate-assisted uncertainty quantification. MD simulations yield GB energies for 27 symmetric tilt boundaries from 0--2000~K, which are consistent with available DFT values. The average GB energy is nearly temperature-independent below 1000~K and increases at higher temperatures. A mechanistic pore-drag model applied to the only available grain growth dataset for actinide nitrides yields a mobility reduction factor of $s \approx 0.93$--$0.99$, statistically indistinguishable from unity, confirming that pore drag is negligible under the experimental conditions. The intrinsic GB mobility is therefore extracted directly from the effective mobility, yielding $M_0 = 2.05\times10^{-15}$~m$^4$/(J$\cdot$s) and $Q_M = 0.89$~eV. Phase-field simulations conducted from 1500--2000~K confirm normal curvature-driven grain growth, with grain size distributions converging to the Hillert-like form. A surrogate-assisted global sensitivity analysis---combining principal component analysis, Gaussian process regression, and Sobol decomposition---reveals that the mobility prefactor $M_0$ dominates output variance at all times, followed by the activation energy $Q_M$, while the GB energy $\gamma$ contributes minimally. These results establish the first quantitative grain growth framework for UN and identify the reduction of uncertainty in $M_0$ and $Q_M$ as the highest-priority target for future experimental efforts.

cond-mat.mtrl-sci↗
arXiv2026

Silicon Solar Cell Design for >30% Efficiency via Singlet Fission

Singlet fission (SF) materials convert high-energy photons into multiple charge carriers, providing a route to exceed the efficiency limits of single-junction silicon solar cells without many of the complexities of multi-junction tandem designs. Following the first demonstration of an SF-enhanced silicon solar cell in 2025, there is a need to understand how SF materials can be effectively integrated into high-efficiency industrial silicon devices and translated from proof of concept to a manufacturable technology. Using coupled optical and electrical simulations, we assess the efficiency potential of several industrially relevant silicon cell architectures combined with SF materials. Interdigitated back-contact (IBC) cells offer the greatest potential for improvement due to unrestricted front-surface access and can achieve efficiencies exceeding 33%. However, performance is highly sensitive to front-surface passivation quality. Appropriate silicon design, particularly controlled surface doping and fixed interfacial charge, can mitigate recombination losses and relax passivation requirements for ultra-thin exciton-transfer layers.

cond-mat.mtrl-sci↗