Surface Interactions Research Articles

Human coronavirus 229E inactivation on porous and nonporous materials using dielectric barrier discharge (DBD) plasma.

Viruses can spread through contaminated aerosols and contaminated surface materials, and effective disinfection techniques are essential for virus inactivation. Nonthermal plasma-generated reactive oxygen and nitrogen species can effectively inactivate the coronavirus. We aim to interpret the coronavirus inactivation level and mechanism of surface interaction with materials with and without dielectric barrier discharge (DBD) plasma treatment. Nonthermal plasma, particularly surface-type DBD plasma, can inactivate human coronavirus 229E (HCoV-229E) on porous (paper, wood, mask) and nonporous (plastic, stainless steel, glass, Cu) materials. Virus inactivation was analyzed using a 50% tissue culture infectivity dose (TCID50) using cell line, flow cytometry, and immunofluorescence. Surfaces contaminated with HCoV-229E were treated at different time intervals (0-5 h) with and without plasma exposure (natural decay in ambient air conditions). HCoV-229E persistence conformed to the following order: plastic > cover glass > stainless steel > mask > wood > paper > Cu with and without plasma exposure. HCoV-229E was more stable in plastic, cover glass, and stainless steel in 5 h, and the viable virus titer gradually decreased from its initial log10 order of 6.892 to 1.72, 1.53, and 1.32 TCID50/mL, respectively, under plasma exposure. No virus was observed in Cu after treatment for 5 h. The use of airflow, ambient nitrogen, and argon did not promote virus inactivation. Flow cytometry and immunofluorescence analysis demonstrated a low expression level of spike protein (fluorescence intensity) during plasma treatment and in E and M genes expression compared with the virus control.

Characterization of ECRH plasmas in TOMAS

To improve the plasma performance and control the density and plasma quality during the flat top phase, wall conditioning techniques are used in large fusion devices like W7-X and in JT60-SA. To study the performance of electron cyclotron wall conditioning, numerous experiments were performed on the TOroidally MAgnetized System, which is operated by LPP-ERM/KMS at the FZ-Jülich. It is a facility designed to study plasma production, wall conditioning, and plasma–surface interactions. The produced electron cyclotron resonance heating plasmas are characterized in various conditions by density and temperature measurements using a movable triple Langmuir probe in the horizontal and the vertical direction, complemented by video and spectroscopic data, to obtain a 2D extrapolation of the plasma parameters in the machine. A way to calibrate the triple Langmuir probe measurements is also investigated. These data can be used to determine the direction of the plasma drift in the vessel and identify the power absorption mechanisms. This will give more insight in the plasma behavior and improve the efficiency of wall conditioning and sample exposure experiments.

Transforming Waste into Wealth: Advanced Carbon-Based Electrodes Derived from Refinery and Coal By-Products for Next-Generation Energy Storage.

This comprehensive review addresses the need for sustainable and efficient energy storage technologies against escalating global energy demand and environmental concerns. It explores the innovative utilization of waste materials from oil refineries and coal processing industries as precursors for carbon-based electrodes in next-generation energy storage systems, including batteries and supercapacitors. These waste-derived carbon materials, such as semi-coke, coal gasification fine ash, coal tar pitch, petroleum coke, and petroleum vacuum residue, offer a promising alternative to conventional electrode materials. They present an optimal balance of high carbon content and enhanced electrochemical properties while promoting environmental sustainability through effectively repurposing waste materials from coal and hydrocarbon industries. This review systematically examines recent advancements in fabricating and applying waste-derived carbon-based electrodes. It delves into the methodologies for converting industrial by-products into high-quality carbon electrodes, with a particular emphasis on carbonization and activation processes tailored to enhance the electrochemical performance of the derived materials. Key findings indicate that while higher carbonization temperatures may impede the development of a porous structure, using KOH as an activating agent has proven effective in developing mesoporous structures conducive to ion transport and storage. Moreover, incorporating heteroatom doping (with elements such as sulfur, potassium, and nitrogen) has shown promise in enhancing surface interactions and facilitating the diffusion process through increased availability of active sites, thereby demonstrating the potential for improved storage capabilities. The electrochemical performance of these waste-derived carbon materials is evaluated across various configurations and electrolytes. Challenges and future directions are identified, highlighting the need for a deeper understanding of the microstructural characteristics that influence electrochemical performance and advocating for interdisciplinary research to achieve precise control over material properties. This review contributes to advancing electrode material technology and promotes environmental sustainability by repurposing industrial waste into valuable resources for energy storage. It underscores the potential of waste-derived carbon materials in sustainably meeting global energy storage demands.

Irrigation strongly influences near‐surface conditions and induces breeze circulation: Observational and model‐based evidence

AbstractIrrigation is becoming increasingly common in agriculture and is essential to meet the growing demand for food. Studies of the impact of irrigated areas on local meteorology reveal a strong influence on near‐surface conditions, although the extent of this influence varies considerably between locations. In addition, though theoretical evidence suggests that irrigation can create breeze‐like atmospheric boundary‐layer circulations, observational evidence is still lacking. This study investigates the effects of irrigation on the surface and atmospheric boundary layer in the Ebro basin, an intensively irrigated area with a semi‐arid climate in northeastern Spain. Observational data from the international field campaign Land Surface Interactions with the Atmosphere over the Iberian Semi‐arid Environment are analysed together with coupled surface–atmosphere model output to better understand and quantify the impact of irrigation on the lower atmosphere. A simple parametrization of irrigation is shown to improve the accuracy of the model. Results demonstrate that irrigation increases the average latent heat flux by over 200 Wm, reduces air temperature by 4.7°C, and increases specific humidity by 50% at 2 m during the day over the irrigated region of the domain. Moreover, irrigation limits convection and strongly stabilizes the atmospheric boundary layer. Notably, the study provides evidence for an irrigation‐induced breeze from the irrigated area to the semi‐arid area. These findings highlight the importance of considering irrigation in numerical models for weather forecasting, climate modelling and sustainable agricultural planning.

Quantifying Contributions of Different Repulsion to Film Drainage Time during the Bubble-Solid Surface Attachment and Implications for the Flotation of Fine Particles.

The flotation recovery of fine particles faces serious challenges due to the lack of kinetic energy required for supporting their radial displacement and attachment with bubbles. Generally, the hydrodynamic resistance and repulsive disjoining pressure successively inhibit the liquid outflow intervening between the bubble and solid surfaces. To quantitatively characterize the influence of the main repulsion on film thinning time, experiments have been designed in three different aqueous systems. Bubble surface mobility closely associated with hydrodynamic resistance was determined by the rising bubble technique, and the DLVO theory was employed to confirm the evolution of electrostatic repulsion. The film drainage process was then measured based on the high-speed microscopic interferometry. Furthermore, the influence of the main repulsion on bubble-solid surface interactions was examined by flotation recovery. Results show that the earlier buildup of hydrodynamic force ran through the whole film thinning process, and under immobile conditions, the central region gradually became dominant in film thinning due to the very limited fluid flow at the thinnest rim position. Therefore, to achieve the identical film thickness (∼100 nm), the large hydrodynamic resistance could prolong the film thinning time by about 1 order of magnitude, compared with that induced by electrostatic repulsion, which accounts for the increased flotation recovery by 10% using mobile bubbles. This study not only enhances the understanding of how typical repulsive forces work in film drainage dynamics but also opens up an avenue for enhancing flotation and avoiding wasting resources by modulating bubble surface mobility and thus micro/nanoscale fluid flow.

Heat transfer during droplet impact on a cold superhydrophobic surface via interfacial thermal mapping

AbstractUndesired heat transfer during droplet impact on cold surfaces can lead to ice formation and damage to renewable infrastructure, among others. To address this, superhydrophobic surfaces aim to minimize the droplet surface interaction thereby, holding promise to greatly limit heat transfer. However, the droplet impact on such surfaces spans only a few milliseconds making it difficult to quantify the heat exchange at the droplet–solid interface. Here, we employ high‐speed infrared thermography and a three‐dimensional transient heat conduction COMSOL model to map the dynamic heat flux distribution during droplet impact on a cold superhydrophobic surface. The comprehensive droplet impact experiments for varying surface temperature, droplet size, and impacting height reveal that the heat transfer effectiveness () scales with the dimensionless maximum spreading radius as , deviating from previous semi‐infinite scaling. Interestingly, despite shorter contact times, droplets impacting from higher heights demonstrate increased heat transfer effectiveness due to expanded contact area. The results suggest that reducing droplet spreading time, as opposed to contact time alone, can be a more effective strategy for minimizing heat transfer. The results presented here highlight the importance of both contact area and contact time on the heat exchange between a droplet and a cold superhydrophobic surface.

The impact of hydroxyapatite crystal structures and protein interactions on bone's mechanical properties

Hydroxyapatite (HAP) constitutes the primary mineral component of bones, and its crystal structure, along with the surface interaction with proteins, significantly influences the outstanding mechanical properties of bone. This study focuses on natural hydroxyapatite, constructing a surface model with calcium vacancy defects. Employing a representative model of aspartic acid residues, we delve into the adsorption mechanism on the crystal surface and scrutinize the adsorption forms of amino acid residues on HAP and calcium-deficient hydroxyapatite (CDHA) surfaces. The research also explores the impact of different environments on adsorption energy. Furthermore, a simplified sandwich structure of crystal-polypeptide-crystal is presented, analyzing the distribution of amino acid residue adsorption sites on the crystal surface of the polypeptide fragment. This investigation aims to elucidate how the stick–slip mechanism of polypeptide molecules on the crystal surface influences the mechanical properties of the system. By uncovering the interface mechanical behavior between HAP and osteopontin peptides, this article offers valuable theoretical insights for the construction and biomimetic design of biocomposites.

Phenolics from Polygonatum cyrtonema Hua extracted using natural deep eutectic solvents combined with auxiliary techniques: Composition, bioactivity, and mechanistic elucidation

This study investigated the natural extraction of polyphenolic compounds from Polygonatum cyrtonema Hua (P. cyrtonema). Employing the combination of natural deep eutectic solvents (NADESs) and auxiliary extraction techniques, we mainly focused on yield, total phenolics, total flavonoids, antioxidant capacity, and enzyme inhibition efficiency. Compared to hot reflux extraction (HRE), the NADES extract using a 1:2 ratio of choline chloride-lactic acid (ChCl-Lac) significantly increased the total phenolic content (TPC), total flavonoid content (TFC), and α-glucosidase inhibition (p < 0.05). The HPLC-MS-MS identified the five most abundant phenolic compounds. Quantitative analysis showed that these compounds had the highest leaching rates in the ultrasonic-assisted extraction (UAE) combined with lactic acid-based NADES system, followed by microwave-assisted extraction (MAE), requiring less than 4 min. Notably, rutin exhibited the highest extraction rate of 281.1 μg/g in the UAE-ChCl-Lac system, 9.82 times higher than conventional methods. The extraction mechanism was elucidated from the perspectives of surface charge density distribution and interaction energy. Therefore, ultrasound or microwave-assisted NADES extraction aligns with sustainable development principles, offering a green approach to enrich polyphenolic compounds in P. cyrtonema.

Trap-n-zap: Electrocatalytic degradation of perfluorooctanoic acid (PFOA) with UiO-66 modified boron nitride electrodes at environmentally relevant concentrations

Poly- and per-fluoroalkyl substances (PFAS) are synthetic chemicals of increasing global concern due to their toxicity and environmental persistence. Hexagonal boron nitride (h-BN) is an electrochemically active semiconductor that generates a hydrophobic electron-hole with a high affinity for the fluorinated tail of perfluorooctanoic acid (PFOA), which enhances surface interactions in aqueous solutions. We demonstrate that h-BN electrocatalytically oxidizes PFOA to shorter chains. The degradation is enhanced by modifying the h-BN surface with an adsorbent, UiO-66 (UiO-66@BN), that facilitates proximal adsorption to catalytic sites (trap-and-zap). At the environmentally relevant concentration of 100 µg/L, electrochemical trap-and-zap removes 99.5% of PFOA with 70% defluorination in 3 h at a pH 4.5. Computational results show that PFOA requires an overpotential of 1.87 V vs. SCE, which is close to the experimental overpotential. The electrical energy per order (EE/O) of UiO-66@BN is 6.1 kWh/m3, indicating that it is a competitive material for PFOA electrochemical remediation.

The Role of Friction in Athletic Performance: A Descriptive Analysis

Friction is a fundamental force that has a substantial impact on athletic performance across all sports disciplines. This descriptive research investigates the varied impact of friction in building athletic skill. This study looks at how friction affects running, jumping, throwing, and other sports activities by examining static and kinetic frictional forces, as well as elements that influence frictional interactions. The research examines the interaction of athletes, footwear, surfaces, and equipment to explain how friction governs propulsion, stability, and efficiency in sports activity. The findings of this study have important significance for players, coaches, and sports scientists, as they provide avenues for optimizing training techniques, equipment design, and performance tactics for increased athletic achievement. Keywords Friction , Athletic Performance , Role , Descriptive Analysis , Surface Friction , Footwear Friction , Sports Science , Biomechanics , Performance Optimization , Surface Interaction , Traction , Stability , Movement Efficiency , Injury Prevention ,Training Strategies

The Physisorbate-Layer Problem Arising in Kinetic Theory of Gas–Surface Interaction

The Physisorbate-Layer Problem Arising in Kinetic Theory of Gas–Surface Interaction

Developing a binary composite of covalent organic framework and gold microstructures: Highly efficient dual-mode catalyst for analysis of nitrophenol isomers and their oxidative products

As a key hazard, nitrophenol and its byproducts are a vital raw material in the industry and potentially released into aquatic environments, which affects the ecosystem and severely threatens living systems. It is crucial to detect nitro-hazards quantitatively and systematically. The unique structures of isomer separation and catalytic reduction are highly complex in a single system, not yet reported detection method. The present report constructed robust gold-microstructures (AuMSs) with bis-triazole-derived covalent organic framework (BTCOF) was developed to analyze the dual-mode application of electrochemical redox signals and catalytic degradation of nitrophenol isomers (NPIs) and their oxidative products. The synergistic interaction of tunable surfaces on binary materials enhanced catalytic efficiency, faster kinetic rates, and poor passivation effect. Based on the variance in pKa values, both NPIs and nitrosophenols (NSPIs) could be identified, peak separated, and sensed simultaneously. A catalyst combined with NaBH4, enabled NPIs reduction within 10 minutes. This proposed electrochemical method achieved a nanomolar LOD (1.82, 1.67, and 1.15 × 10−9 M for o-, m-, and p-NPs), excellent sensitivity to ultrawide linear range concentrations while being selective, and reproducible. Moreover, AuMSs-BTCOF/GCE detected NPIs in the industrial effluents and biofluids with recovery rates between 94.70 to 99.95 ± 0.18 % with RSD of 2.86 %. The electrochemical result was validated by conventional method with proven statistical analysis (error 4.02 %). In the catalytic reduction of NPIs, the catalyst is more than 89.24 % efficient, and durable stability. The designed system has proven to be an effective, sensitive, and accurate dual-detection tool for monitoring environmental targets and diagnosing diseases.

Study on the Wettability and Methane Desorption Characteristics of Coal under High Pressure with Different Surfactants.

In the process of coalbed methane extraction, due to the strong hydrophilicity of coal, the surface interaction force between water and the coal matrix is strong. The hydrophobic effect of the coal seam during drainage and pressure reduction is not significant, and adsorbed methane is difficult to desorb. In order to reduce the surface interaction force promoting methane desorption between water and coal, the surfactants NH766, G526, and D001 with a concentration of 0.1% were selected. A pressure of 12 MPa, which is close to that used for the on-site mining of coalbed methane in Baode, was selected as the experimental condition to simulate hydraulic fracturing of high fat coal, and the influence of different surfactants on methane desorption characteristics was analyzed. Combining contact angle experiments and infrared spectroscopy experiments, we explored the changes in wettability of the coal samples. We compared the changes in wettability and methane desorption characteristics and explored the similarities between these changes. The experimental results showed that after NH766 treatment, the content of oxygen-containing functional groups in coal rock decreased by 30%, and the contact angle of the coal matrix surface increased by 10°. Furthermore, its hydrophobicity was enhanced, and the desorption amount increased by 24%. In contrast, the oxygen-containing functional groups in coal rock after G526 and D001 treatments increased by 5% and 16%, respectively, and the contact angle of the coal matrix surface became smaller. Furthermore, its hydrophilicity was enhanced, and the desorption amount was reduced by 12.5% and 20%, respectively. NH766 reduces wettability and promotes methane desorption, and it can be applied to improve CBM extraction efficiency. G526 and D001 enhance wettability and inhibit methane desorption, which make them suitable for dust prevention and gas control in coal mines.

Fracture behavior of composite piezoelectric intelligent structures formed by pasting MFC based on serial multi-scale method

The composite piezoelectric intelligent structures formed by combining piezoelectric materials with composite materials can achieve state perception and deformation control of the structure. Based on the molecular dynamics method, the continuum finite element method and the cohesive force model, the serial multi-scale research on the bonded composite piezoelectric intelligent structure was carried out from the micro, meso and macro scales. Molecular models of adhesive, macro fiber composite (MFC) surface and composite surface were established. The effects of temperature and pressure on the surface interaction energy of adhesive/MFC and adhesive/composite materials were analyzed. The traction-separation (T-S) relationship of cohesive region was obtained by virtual stretching method. Combined with the microscopic observation of the mesoscopic adhesive layer, the representative volume element (RVE) model of the mesoscopic adhesive layer considering the bubble defect was established, and the cohesive relationship curve of the adhesive layer was obtained. A double cantilever beam (DCB) macro finite element model was established to simulate the crack propagation behavior of the adhesive layer, and compared with the experimental results.

Luminescence of Lanthanide Complexes in Mesoporous Silica Matrices: A Textbook Example of Tris‐Dipicolinate Europium Complex Adsorbed in SBA‐15

AbstractThe incorporation of luminescent lanthanide complexes in inorganic matrices opens appealing possibilities in the rational upstream conception of new luminescent materials with easier recyclability. In this regard, the influence of SBA‐15 mesoporous silica, as a host matrix, on the photophysical properties of europium‐trisdipicolinate cesium salt is investigated. The lanthanide complex can be completely and reversibly adsorbed on the silica, using incipient wetness impregnation (IWI) in WATER, without the need of anchoring groups or covalent bonding on the silica surface. This specific procedure allows the homogeneous dispersion of the lanthanide complex into the host silica matrix. Appropriately assessing the photophysical properties of the targeted luminescent material proved remarkably challenging, demanding utmost caution, particularly due to the strong scattering of the mesoporous matrices. Additionally, while the observations confirm an important increase of luminescence lifetimes of lanthanide complexes upon integration into these mediums, this variation is attributed to the differing refractive indexes and not to specific surface interactions or confinement effect. Indeed, it appeared that previous literature precedents depicted erroneous exhalations of the complexes intrinsic quantum yield due to the repeated use of erroneous refractive index values. In the meantime, the luminance of these materials under UV irradiation improves drastically in comparison to what is obtained with the physical dispersion of micro‐crystals of the lanthanide complex onto silica. It is demonstrated that this improvement is due to a reduced inner filter effect in the adsorbed samples. In this regard, IWI of lanthanide complexes in the mesoporous matrices method could be of interest in the development of recyclable emitting layers, less demanding in terms of emitter quantity.

Comparative analysis of CO2 and N2 adsorption on zeolite 4A: Thermodynamics parameters and site energy distribution investigations

Adsorption equilibrium data for CO2 and N2 on zeolite 4A were volumetrically measured at temperatures ranging from 278 K to 328 K and gas pressures up to 4 MPa. The experimental data was correlated using the high-pressure Langmuir, Sips, and DA adsorption isotherm models. The high-pressure DA model was found to be the optimal model for describing the adsorption isotherms on basis of nonlinear regression analysis. Subsequently, the thermodynamic parameters, including isosteric heat of adsorption (Hst), adsorption phase specific heat capacity (cpa), adsorption phase entropy (sa), and enthalpy (ha), considering the actual adsorption state, were estimated. The results demonstrate that the adsorption of CO2 on zeolite 4A is greater than that of N2. The higher Hst and ha values and the lower sa values of CO2 compared to N2, suggest a stronger surface interaction of CO2 with zeolite 4A, resulting in a more ordered arrangement of CO2 molecules than N2. Site energy distribution theory analysis indicates that less energy is required for CO2 adsorption and greater site energy heterogeneity of CO2 than those of N2 on zeolite 4A. The obtained results evidence that the studied zeolite 4A could be a promising candidate adsorbent for greenhouse gas capture.

Satellite design optimization for differential lift and drag applications

AbstractUtilizing differential atmospheric forces in the very low earth orbits (VLEO) regime for the control of the relative motion within a satellite formation is a promising option as any thrusting device has significant impact on system design due to the limited weight and size restrictions of small satellites. One possible approach to increase the available accelerations caused by the atmosphere is to reduce the mass of the respective satellites as well as to increase the available surface area. However, satellites of these characteristics suffer from rapid orbital decay and consequently have a reduced service lifetime. Therefore, achieving higher control forces is in contradiction to achieving a minimum orbital decay of the satellites, which currently represents one of the biggest challenges in the VLEO regime. In this article, the geometry of a given reference satellite, a 3UCubeSat, is optimized under the consideration of different surface material properties for differential lift and drag control applications while simultaneously ensuring a sustained VLEO operation. It is worth noting that both the consideration of sustainability as well as the optimization with regard to differential lift are new in literature. It was shown that the advantageous geometries strongly depend on the type of gas–surface interaction and thus, two different final designs, one for each extreme type, are presented. In both cases, improvements in all relevant parameters could be achieved solely via geometry adaptions.

Mechanistic evaluation of contrasting modulation in conformation and catalytic performance of urease by surface interaction of graphene oxide and amine- functionalized graphene oxide nanosheets

The increasing use of graphene-based nanomaterials raises concerns about their potential environmental impact as ecotoxicants. This article examines the interaction and effects of graphene oxide (GO) and its amine-derived (GONH2) 2-D nanosheets on urease dynamics, a crucial enzyme in soil nutrient cycling, through spectroscopic, microscopic, and computational analyses. The findings reveal the distinct interaction mechanisms: GO formed ground - and excited-state complexes with urease; thus, fluorescence quenching was static and dynamic via hydrophobic interaction. In contrast, GONH2 nanosheets formed a ground-state complex by static quenching involving Van der Waals and hydrogen bonding. These interactions were energetically favored and altered tryptophan (Trp) residues’ microenvironment more than tyrosine (Tyr). The average exciton lifetime of urease in the presence of GO have decreased from 4.34 ns to 3.647 ns at the mere concentration of 7.11 µM, while for GONH2, no discernable change (4.16 ns) was observed even at the concentration of 16.75 µM. Primarily, the strong interaction of GO leads to the rearrangement of polypeptide structure, reduced α-helices to 12 %, and increased β-sheets by six times. In contrast, with GONH2, α-helices were reduced to 79 %, and β-sheets were increased by 1.8 times at the similar concentration. Molecular docking revealed that neither GO nor GONH2 interacted with the active site of urease, and binding was primarily via hydrophobic, Van der Waals, and hydrogen bonding, concurrent with in-vitro incubation results. Positive total energy (3.85 kJ mol−1) during molecular docking analysis of urease-GO interaction and inhibition in enzyme activity to 62 %, altered Vmax value (0.04606 ± 0.001 mM/s), without affecting the Km (4.78045 ± 0.12 mM) suggested that inhibition was noncompetitive and steric clashes due to disruptive binding might drove the inhibition. Meanwhile, negative total internal energy (-3.97 kJ mol−1) during urease + GONH2 binding and enhanced enzymatic activity by 32 % in-vitro without altering Vmax (0.063091 ± 0.003 mM/s) and Km (4.953943 ± 0.2 mM) values suggested that urease's binding site was well-complemented by GONH2 nanosheets, serving as a redox-mediator and radical-quencher.

Hydrological drought assessment using the standardized groundwater index and the standardized precipitation index in the Berg River Catchment, South Africa

Study regionBerg River Catchment (BRC), South Africa (SA). Study focusHydrological droughts threaten water security and climate Change and groundwater abstractions may exacerbate their impact. Thus, early detection and prediction of droughts is essential. The integration of the Standardised Groundwater Index (SGI) with the Standardised Precipitation Index (SPI), has been applied worldwide, it but not explored in South Africa (SA). The aim of this study was to evaluate the integration of the SGI and SPI for hydrological drought assessment within the BRC, SA. New hydrological insights for the regionThe sensitivity of the SGI to selected Probability Distribution Functions (PDFs) was examined, resulting in the Gamma and Log-Normal PDFs being preferred in the BRC. SGI-Gamma and SPI-Gamma comparisons validated the SGI method and shed light on the key factors influencing groundwater-related droughts in the BRC. The following was revealed: Hydrological droughts in the BRC are influenced by climate factors, surface and groundwater interactions, and groundwater abstractions. When conducting hydrological drought assessments using the SGI and the SPI, the initial focus should be on catchment-scale assessments before expanding to national-scale evaluations. Groundwater in the BRC exhibit significant resilience to droughts induced by climate factors, and thus useful to mitigate the risk of future droughts. Finally, The SGI performed satisfactorily in the BRC with limited groundwater level data.

Electron Donor-Specific Surface Interactions Promote the Photocatalytic Activity of Metal-Semiconductor Nanohybrids.

In the past two decades, the application of colloidal semiconductor-metal nanoparticles (NPs) as photocatalysts for the hydrogen generation from water has been extensively studied. The present body of literature studies agrees that the photocatalytic yield strongly depends on the electron donating agent (EDA) added for scavenging the photogenerated holes. The highest reported hydrogen production rates are obtained in the presence of ionic EDAs and at high pH. The large hydrogen production rates are attributed to fast hole transfer from the NP onto the EDAs. However, the present discussions do not treat the influence of EDA-specific surface interactions. This systematic study focuses on that aspect by combining steady-state hydrogen production measurements with time-resolved and static optical spectroscopy, employing 11-mercaptoundecanoic acid-capped, Pt-tipped CdSe/CdS dot-in-rods in the presence of a large set of EDAs. Based on the experimental results, two distinct EDA groups are identified: surface-active and diffusion-limited EDAs. The largest photocatalytic efficiencies are obtained in the presence of surface-active EDAs that induce an agglomeration of the NPs. This demonstrates that the introduction of surface-active EDAs can significantly enhance the photocatalytic activity of the NPs, despite reducing their colloidal stability and inducing the formation of NP networks.