No abstract

With recent advances in the field of single‐atoms (SAs) used in photocatalysis, an unprecedented performance of atomically dispersed co‐catalysts has been achieved. However, the stability and agglomeration of SA co‐catalysts on the semiconductor surface may represent a critical issue in potential applications. Here, the photoinduced destabilization of Pt SAs on the benchmark photocatalyst, TiO2, is described. In aqueous solutions within illumination timescales ranging from few minutes to several hours, light‐induced agglomeration of Pt SAs to ensembles (dimers, multimers) and finally nanoparticles takes place. The kinetics critically depends on the presence of sacrificial hole scavengers and the used light intensity. Density‐functional theory calculations attribute the light induced destabilization of the SA Pt species to binding of surface‐coordinated Pt with solution‐hydrogen (adsorbed H atoms), which consequently weakens the Pt SA bonding to the TiO2 surface. Despite the gradual aggregation of Pt SAs into surface clusters and their overall reduction to metallic state, which involves >90% of Pt SAs, the overall photocatalytic H2 evolution remains virtually unaffected.

We present a comprehensive structural and analytical characterization of the highly promising supported catalytically active liquid metal solutions (SCALMS) system. This novel catalyst shows excellent performance for alkane dehydrogenation, especially in terms of resistance to coking. SCALMS consists of a porous support containing catalytically active low-melting alloy particles (e.g., Ga-Pd) featuring a complex structure, which are liquid at reaction temperature. High-resolution 3D characterization at various length scales is required to reveal the complex pore morphology and catalytically active sites’ location. Nano X-ray computed tomography (nano-CT) in combination with electron tomography (ET) enables nondestructive and scale-bridging 3D materials research. We developed and applied a correlative approach using nano-CT, 360°-ET and analytical transmission electron microscopy (TEM) to decipher the morphology, distribution and chemical composition of the Ga-Pd droplets of the SCALMS system over several length scales. Utilizing ET-based segmentations of nano-CT reconstructions, we are able to reliably reveal the homogenous porous support network with embedded Ga-Pd droplets featuring a nonhomogenous elemental distribution of Ga and Pd. In contrast, large Ga-Pd droplets with a high Ga/Pd ratio are located on the surface of SCALMS primary particles, whereas the droplet size and the Ga/Pd ratio decreases while advancing into the porous volume. Our studies reveal new findings about the complex structure of SCALMS which are required to understand its superior catalytic performance. Furthermore, advancements in lab-based nano-CT imaging are presented by extending the field of view (FOV) of a single experiment via a multiple region-of-interest (ROI) stitching approach.

Hierarchical pore structures exhibit morphological features on several length scales, which govern important materials properties in catalysis, such as catalytic activity, diffusivity or selectivity. Correlative tomography offers unique opportunities for a comprehensive and scale‐bridging 3D characterization of such complex pore morphologies, which is crucial to further optimize materials design and synthesis routines. This study explores the capabilities of correlative 360° electron tomography (ET) and lab‐based nano X‐ray computed tomography (Nano‐CT) enabling 3D analyses of volumes of up to (60 µm)³ with down to nm resolution, as demonstrated for zeolite particles with embedded macropores. By first applying the two techniques to the same particle the higher resolution and fidelity of ET are used to improve the segmentation of pore space in the Nano‐CT reconstruction. Extended statistical relevance and access to interparticle pore space are obtained from reconstructions of larger particle agglomerates, using the large‐field‐of‐view mode of the Nano‐CT. The presented correlative approach enables real space analyses of important pore characteristics for comparison with complementary pore characterization techniques. Moreover, by investigating samples from different stages of the synthesis, 360°‐ET and Nano‐CT provide unique insights into the formation mechanism of porous materials, as demonstrated for the steam‐assisted crystallization of the macroporous zeolite particles.

No abstract