High Vapor Pressure Research Articles

Divergent Drivers of Declining Urban Vegetation Productivity and Transpiration During Heatwaves

AbstractHeatwave events, characterized by high vapor pressure deficit (VPD) and low soil moisture (SM), considerably disrupt the regional carbon and water cycle. However, research pertaining to the impact of heatwaves on vegetation productivity (VPu) and vegetation transpiration (VTu), along with their underlying drivers, particularly in urban areas, remains limited. This study investigates the response of VPu and VTu to heatwave events across 895 global cities from 1990 to 2022. The analysis reveals a notable upward trend in the average heatwave frequency, intensity, and duration across the global cities. Heatwave events demonstrate a detrimental impact on VPu and VTu, resulting in an average decrease of 28% and 26%, respectively, during heatwave occurrences. The attribution analysis reveals divergent driving factors for the decline in VPu and VTu during heatwaves. The decrease in VPu is primarily influenced by SM, contributing 60% to the downward trend of VPu during heatwaves. Notably, VPu displays a sharp downward trend when SM falls below 0.38 m3/m3. In contrast, the primary driver of VTu decline is VPD, contributing more than 66% to the downward trend of VTu during heatwave events. VTu exhibits a significant downward trend when VPD exceeds 1.35 kPa. The results of this study show the important effects of increasingly frequent heatwaves on vegetation transpiration and productivity, and that can be used as quantitative factor to be evaluated when investigating policy measures for the resilience of urban areas.

Impacts of California Wildfires on CO2 and Other Trace Gases

AbstractWildfires have broad impacts on the atmosphere, ecology, and society. This study leverages satellite data and chemistry‐transport models to analyze the impact of wildfires on trace gases in California during the August‐October periods of 2018, 2019, and 2020. During these months, Southern California experiences minimal precipitation, leading to a high Vapor Pressure Deficit, which results in decreased photosynthetic activities. This reduction, combined with increased biomass burning, causes a rise in CO2 concentrations. Increased CO and CH4 levels are also seen in TROPOMI retrievals tied to the increase in biomass burning. The CarbonTracker model captures these elevated CO2 concentrations, though with a reduced amplitude of increased CO2. Similarly, the GEOS‐Chem model successfully simulates high CO levels but underestimates the observed enhancements. These findings will improve the understanding of fire's influence on trace gases and refine future numerical models on surface emissions and transport.

Decoupling of Tree‐Ring Cellulose δ18O and δ2H Highlighted by Their Contrasting Relationships to Climate and Tree Intrinsic Variables

ABSTRACTOxygen (δ18O) and hydrogen (δ2H) stable isotope ratios are tightly coupled in precipitation and, albeit damped, in leaf water, but are often decoupled in tree‐ring cellulose. The environmental and physiological conditions in which this decoupling occurs are not yet well understood. We investigated the relationships between δ18O and δ2H and tree‐ring width (TRW), tree crown volume, tree age and climate in silver fir and Douglas‐fir and found substantial differences between δ18O and δ2H. Overall, δ18O–δ2H correlations were weak to absent but became significantly negative under high summer vapour pressure deficit (VPD). δ18O and δ2H had positive and negative nonlinear relationships with TRW, respectively, with clear relationships at the site and tree levels for silver fir and, to a lesser extent, for Douglas‐fir. Age trends for silver fir were weakly negative in δ18O but positive in δ2H. Tree crown volume and δ18O or δ2H had no significant relationships. Most strikingly, δ18O strongly depended on spring climate (precipitation and VPD), whereas δ2H depended on summer climate (temperature and VPD) for both species. Our study shows that the δ18O–δ2H decoupling in tree‐ring cellulose in two temperate conifer species could be highlighted by their contrasting relationships to climate and tree intrinsic variables (TRW, age).

Mapping Climatic Regions of the Cerrado: General Patterns and Future Change

ABSTRACTThe Cerrado biome, renowned for its biodiversity and threatened by rapid land transformation, encompasses a vast savanna ecosystem in Brazil. The region is characterised by a seasonal climate, influenced by a myriad of meteorological systems creating diverse and non‐homogeneous rainfall regimes across the region. To account for this heterogeneity, we propose a novel classification of the Cerrado using rainfall data to delineate three distinct climatic regions: Eastern, Southern and Central‐West Cerrado. The Eastern region exhibited the driest and most seasonal climate, marked by high vapour pressure deficit (VPD) and predominantly open‐canopy vegetation. Conversely, the Southern region, characterised by lower seasonality, boasts a higher proportion of forest cover and lower mean VPD. The Central‐West region, encompassing diverse landscapes, featured areas with higher precipitation levels, particularly along the Amazônia border. Furthermore, we conducted trend analyses on observed station data and used CMIP6 models to evaluate future scenarios under differing emissions trajectories. While observed trends in mean rainfall were marginal, VPD demonstrated a notable upward trend of approximately 1% annually throughout the biome. Climate models indicated a substantial drying close to the Amazônia border, and wetter conditions in the southeast. All Cerrado regions are anticipated to experience amplified seasonality and VPD, with VPD projected to surge by approximately 30% (60%) under low (high) emissions scenarios by the end of the century. Notably, the transition from the dry to wet season was the most affected. Our study provides critical insights on how the climatic heterogeneity of the Cerrado shapes vegetation structure distribution and how future changes will exacerbate water stress throughout the biome. These findings underscore the importance of understanding climate variability for effective conservation and management strategies in the region.

On the product phases and the reaction kinetics of carbothermic reduction of UO2+C at relatively low temperatures

The synthesis of UC using carbothermic reduction of UO2 and C mixtures has been well studied at high temperatures. However, the product phase behavior of carbothermic reduction at low temperatures (≤1773 K) is not well studied. Such a study is important as low temperatures permit single phase UC synthesis without forming secondary higher carbides, and it further supports the knowledge base of the process that needs to be used for transuranic elements such as plutonium that have high vapor pressures at elevated temperatures. Therefore, a low temperature carbothermic reduction of two different C/UO2 molar ratios under inert and reducing environments have been studied here. Two different sample holding crucibles, alumina (Al2O3) and graphite, were also used here to differentiate the hypostoichiometric (UC1-a) and oxygen dissolved (UC1-xOx) uranium monocarbide phases adding more details on the two systems. Also, the reaction kinetics involved in the formation of UC via the carbothermic reduction of UO2+C using product phases instead of evolved gases such as carbon monoxide is reported here. Under inert atmospheres but with significant oxygen partial pressures, the low temperature carbothermic reduction of UO2+C produced up to 90 wt.% UC1-xOx type oxycarbides as was confirmed by Xray powder diffraction. Reducing Ar-4%H2 environments at these temperatures were not successful in synthesizing UC as it reduces the amount of C required for the carbothermic reduction, leaving UC phase at a non-equilibrium state. Inert atmospheres with low or negligible oxygen partial pressures on the other hand produced near stoichiometric UC at high phase purity, especially at 1673 – 1773 K temperature range. An activation energy of 377±75 kJmol-1 was also calculated using product phase concentrations of the carbothermic reduction of UO2+C under these inert Ar(g) atmospheres.

Factors that influence the migration of sorbed pesticides in polyethylene and biodegradable mesoplastics

Trifluralin, Chlorpyrifos, and Procymidone migration performance from polyethylene (PE) and biodegradable (Mater-Bi: M-B) mulching films was examined. Desorption of pesticides from PE and M-B was studied using soil-plastic microcosms, considering temperature, soil humidity, and mulching film type as experimental variables. Trifluralin and Chlorpyrifos desorption was higher for PE than for M-B under all experimental conditions. In both cases, as the temperature increased from 25º C to 40º C, pesticide migration also increased, whereas as the soil humidity raised from 30% to 60%, pesticide desorption decreased. In the case of Procymidone, migration from PE and M-B at 25º C was similar under both soil moisture conditions. Migration percentages were similar for both mulch films at 40ºC and 30% soil humidity. However, at higher soil moisture (60%), migration from M-B was greater than from PE. A linear relationship was observed between the percentage of migration and the vapor pressure of the pesticides. In all cases, migration increased with higher vapor pressure, indicating a possible migration mechanism in the vapor phase. Pesticide migration increased at high temperatures (40º C). The effect of soil humidity in reducing pesticide migration was more significant at lower levels (30%).In addition, the mesoplastic sorption of pesticides in soil columns was studied using PE and M-B films. While the recoveries for Trifluralin, Chlorpyrifos, and Procymidone in the PE films were 0.05% ± 0.01%, 0.13% ± 0.03%, and non-detectable, the recoveries for M-B were: 0.49% ± 0.07%, 0.31% ± 0.09%, and 0.17% ± 0.10%, respectively, indicating that M-B was a better adsorbent than PE in all cases. This behavior should be considered in combination with the lower migration percentages observed for this type of mulching film in the microcosm experiments. These results could indicate a potential carrier effect of pesticide on biomesoplastic in the environment.

A matrix-centered view of mass spectrometry platform innovation for volatilome research.

Volatile organic compounds (VOCs) are carbon-containing molecules with high vapor pressure and low water solubility that are released from biotic and abiotic matrices. Because they are in the gaseous phase, these compounds tend to remain undetected when using conventional metabolomic profiling methods. Despite this omission, efforts to profile VOCs can provide useful information related to metabolic status and identify potential signaling pathways or toxicological impacts in natural or engineered environments. Over the past several decades mass spectrometry (MS) platform innovation has instigated new opportunities for VOC detection from previously intractable matrices. In parallel, volatilome research linking VOC profiles to other forms of multi-omic information (DNA, RNA, protein, and other metabolites) has gained prominence in resolving genotype/phenotype relationships at different levels of biological organization. This review explores both on-line and off-line methods used in VOC profiling with MS from different matrices. On-line methods involve direct sample injection into the MS platform without any prior compound separation, while off-line methods involve chromatographic separation prior to sample injection and analyte detection. Attention is given to the technical evolution of platforms needed for increasingly resolved VOC profiles, tracing technical progress over time with particular emphasis on emerging microbiome and diagnostic applications.

Analysis of the performance enhancement of dual-pressure organic flash cycle using a split-flow evaporator and an ejector driven by low-grade energy

To reduce the irreversibility of the throttling in a dual-pressure organic flash cycle (DOFC), this study presents a modified DOFC integrating a split-flow evaporator and an ejector (EE-DOFC). In the EE-DOFC, the flow from the preheater flows into the split-flow tank (ST) and then is split into two parts. One part enters the split-flow evaporator. The other part enters the ejector and entrains the high-pressure (HP) turbine exhaust vapor. The effects of the evaporation pressure, ejector entrainment ratio, and HP turbine outlet pressure on the EE-DOFC performance are studied. The performances of the DOFC, and EE-DOFC are compared under the maximum net power output conditions. The results reveal that after the split-flow evaporator and ejector are integrated, the irreversibility of the pump and mixer decreases and the exergy losses of the ejector and heat exchanger of the EE-DOFC become lower than those of the throttling valves and heat exchanger of the DOFC. The exergy loss of the discharged water is lower in the EE-DOFC than in the DOFC. The net power output and the corresponding levelized cost of electricity (LCOE) of the EE-DOFC are higher by 10.72 % and lower by 10.92 %, respectively, compared with those of the DOFC.

Superconductivity in mercurides of strontium

A large variety of chemical and physical properties are exhibited by mercurides and amalgams. In this work, we have successfully examined seven strontium mercurides: SrHg11, SrHg8, Sr10Hg55, SrHg2, SrHg, Sr3Hg2, and Sr3Hg. The interest in the mercury-rich region is motivated by the large number of mercury-based superconductors that have high mercury content. At the same time, the preparation on the mercury-rich side of the binary phase diagram is experimentally non-trivial, due to the high vapor pressure of mercury and extreme air-sensitivity of mercury-rich compounds. By employing a set of specialized techniques, we were able to discover superconductivity in three mercury-strontium compounds – SrHg11 (Tc=3.2±0.3 K, Hc2=0.18±0.05 T), SrHg8 (Tc=3.0±0.1 K, Hc2=0.35±0.02 T), and Sr10Hg55 (Tc=2.2±0.25 K, Hc2=0.54±0.05 T).

Low‐temperature bubble formation in silica glass

AbstractPhase separation was observed in silica glass following low‐temperature heat treatment in high water vapor pressure through the formation of bubbles. Although the 6 day diffusion treatment in saturated water vapor pressure at 250°C does not normally cause phase separation, the reactive fracture surface and subsurface damage caused by polishing with cerium oxide (CeO2) allowed for an increase in water absorption during treatment and heterogeneous nucleation of the bubbles at damaged sites. The sub‐surface damage, characteristic of blunt contact damage, was only revealed when the polished sample was etched. The formation of bubbles and polishing damage were observed in two silica glasses—one containing chlorine impurities and the other containing OH impurities. Raman spectra collected after fracture or polishing and water diffusion treatment demonstrated an increase in the abundance of –OH species including silanol (SiOH) groups and an evolution in the glass structure in the bubble regions compared with the bubble‐free regions. These results indicate an increase in the reactivity between water and glass fracture surfaces relative to the bulk.

Impacts of High Temperature and Vapor Pressure Deficit on the Maize Opened Spikelet Ratio and Pollen Viability

High temperatures (HTs) and high vapor pressure deficits (VPDs) have significant impacts on maize yields, partly due to the high sensitivity of maize tassels. However, there are few studies quantifying the impacts of HTs and VPDs on maize tassel performance under changing environments. Therefore, we carried out a two-year field experiment that included 20 inbred lines and four sowing dates. Compared with the first sowing date, the seed set in the second sowing date decreased by ~80% in both years. The opened spikelet ratio (OSR) and pollen viability (PV) were the key determinants of seed set, and their respective correlation coefficients with seed set were 0.58 and 0.90. The OSR and PV decreased by ~20% and ~50%, respectively, under high-temperature stress. When Tmax exceeded 32.5 °C or the VPD exceeded 0.91 KPa, PV began to decline; when Tmax exceeded 33.8 °C or VPD exceeded 1.10 KPa, the OSR began to decline. The OSR was more dependent on genotypic background than PV (28.4% vs. 19.7%). The maize tassel water content was significantly correlated with the OSR and PV. Based on the OSR and PV values, the 20 genotypes were divided into three different groups, namely the high H, middle M, and low L groups. The H group, on average, had the highest kernel number per ear and seed set, followed by the M and L groups. The average seed sets of the H, M, and L genotypes under the second sowing date were 17.4%, 10.9%, and 0%, respectively, in 2019 and 13.8%, 7.9%, and 0.6%, respectively, in 2020. The present results indicate that selecting maize varieties with a high OSR is an effective approach for improving maize yield under heat stress.

Global influence of soil texture on ecosystem water limitation

Low soil moisture and high vapour pressure deficit (VPD) cause plant water stress and lead to a variety of drought responses, including a reduction in transpiration and photosynthesis1,2. When soils dry below critical soil moisture thresholds, ecosystems transition from energy to water limitation as stomata close to alleviate water stress3,4. However, the mechanisms behind these thresholds remain poorly defined at the ecosystem scale. Here, by analysing observations of critical soil moisture thresholds globally, we show the prominent role of soil texture in modulating the onset of ecosystem water limitation through the soil hydraulic conductivity curve, whose steepness increases with sand fraction. This clarifies how ecosystem sensitivity to VPD versus soil moisture is shaped by soil texture, with ecosystems in sandy soils being relatively more sensitive to soil drying, whereas ecosystems in clayey soils are relatively more sensitive to VPD. For the same reason, plants in sandy soils have limited potential to adjust to water limitations, which has an impact on how climate change affects terrestrial ecosystems. In summary, although vegetation–atmosphere exchanges are driven by atmospheric conditions and mediated by plant adjustments, their fate is ultimately dependent on the soil.

Stomatal closure as a driver of minimum leaf conductance declines at high temperature and vapor pressure deficit in Quercus.

Rising global temperatures and vapor pressure deficits (VPD) are increasing plant water demand and becoming major drivers of large-scale plant mortality. Controlling transient leaf water loss after stomatal closure (gmin) is recognized as a key trait determining how long plants survive during soil drought. Yet, substantial uncertainty remains regarding how gmin responds to elevated temperatures and VPD and the underlying mechanisms. We measured gmin in 24 Quercus species from temperate and Mediterranean climates to determine if gmin was sensitive to a coupled temperature and VPD increase. We also explored mechanistic links to phenology, climate, evolutionary history, and leaf anatomy. We found that gmin in all species exhibited a non-linear negative temperature and VPD dependence. At 25°C (VPD = 2.2 kPa), gmin varied from 1.19 to 8.09 mmol m-2 s-1 across species but converged to 0.57 ± 0.06 mmol m-2 s-1 at 45°C (VPD = 6.6 kPa). In a subset of species, the effect of temperature and VPD on gmin was reversible and linked to the degree of stomatal closure, which was greater at 45°C than at 25°C. Our results show that gmin is dependent on temperature and VPD, is highly conserved in Quercus species, and is linked to leaf anatomy and stomatal behavior.

Investigation of fuel temperature and injection timing effects on ammonia direct injection in an optical engine

This work investigates the effects of fuel temperature and injection timing on ammonia direct injection in an optical engine using a multi-hole injector. Flash-boiling may occur over various engine-relevant conditions due to ammonia’s high vapor pressure. This phenomenon impacts spray characteristics and, in severe cases, facilitates cavitation inside the nozzle. Both fuel temperature and injection timing (i.e., ambient conditions during injection) impact the intensity of flash-boiling during fuel injection. Therefore, this work varies fuel temperature (from 320K to 388K) and injection timing (from −60CADaTDC (crank angle degrees after top dead center) to −6CADaTDC) to assess their impact on injection mass flux, discharge coefficients, and macroscopic spray characteristics using an ammonia injection pressure of 200bar. For this purpose, the injection mass is measured by analyzing exhaust gas compositions during engine operation with ammonia injections but without combustion. In addition, diffuse background illumination (DBI) images capture the liquid phase of the fuel spray to characterize spray behavior. The findings reveal that increasing fuel temperature decreases ammonia’s injection mass by up to 12.8% but has little impact on discharge coefficients for late injection timings and high in-cylinder pressures. However, discharge coefficients decrease by up to 17.4% (from 0.58 to 0.48) for early injection timings if fuel temperatures are high. The individual sprays of the 6-hole GDI injector may collapse into a uniform spray at high-density conditions without flash-boiling or under strongly flash-boiling conditions. The findings clarify the impact of ammonia’s high vapor pressure on injection mass and prove the relevance of different spray collapse mechanisms in ammonia direct injection engines.

A revision of the Ni-Zn phase diagram based on vapor-solid diffusion experiments

The technique of vapor-solid diffusion couples was systematically studied for its potential in phase diagram investigation using the well-established Ni-Zn system which is highly suitable for this purpose due to the high vapor pressure difference of the two constituents. More than 50 samples synthesized by direct vapor-solid reaction, varying the parameters temperature, time and overall system composition, were investigated by SEM/EDX focusing on diffusion profile line-scans. Supporting powder-XRD and DTA experiments were performed as well. Based on these experimental results, significant changes to the currently accepted Ni-Zn phase diagram, specifically concerning the β, β1, and γ phase fields, are proposed. Furthermore, a relatively simple experimental procedure to prepare vapor-solid diffusion experiments is introduced and its application in phase diagram investigation is discussed in detail.

Interaction of liquid titanium with zirconates and titanates of some alkaline earth metals

Abstract The article presents the results of a study of the interaction of titanium melt with of zirconates BaZrO3 and SrZrO3, as well as titanate SrTiO3 under vacuum conditions and in an inert atmosphere at normal pressure. An original titanium heating method was used during the experiments. It eliminated the melt circulation at the interface between the solid and liquid phases. The method was based on resistive electrical heating of a Grade 2 titanium alloy rod or strip pressed into BaZrO3, SrZrO3 and SrTiO3 powders. Studied the structure, elemental, and phase composition of the products formed during various (up to 300 s) contact of titanium melt with surface zirconates and titaniums. The phase composition was compared with the products obtained by heating compacts from a mixture of titanium powders with BaZrO3, SrZrO3 and SrTiO3 powders. It was shown based on the results obtained that titanium, upon contact with these ceramic materials dissolves zirconium and oxygen and reduces barium and strontium to a metallic state. Barium and strontium evaporated due to the high vapor pressure at the experimental temperature, and caused the melt to splash or form a vapor layer that reduced the interaction rate of the melt with the ceramic. When a titanium melt interacted with BaZrO3 and SrZrO3 intermediate phases were not formed in quantities sufficient for their identification. The Sr3Zr2O7 phase was formed in small quantities during heating a mixture of Ti+SrZrO3 powders. When a titanium melt interacted with SrTiO3, a layer of an intermediate phase was formed, similar in composition to TiO2. Equations for the chemical reaction of the interaction of titanium with the indicated zirconates and titanate were compiled based on the experimental data obtained. It has been shown that titanium melt weted the surface of BaZrO3, SrZrO3 powders well and poorly weted the surface of SrTiO3 powder.

Exposure patterns and the risk factors of Crimean Congo hemorrhagic fever virus amongst humans, livestock and selected wild animals at the human/livestock/wildlife interface in Isiolo County, upper eastern Kenya.

Crimean Congo hemorrhagic fever (CCHF) is a tick-borne zoonotic disease caused by CCHF virus (CCHFV). The disease has a complex transmission cycle that involves a wide range of hosts including mammalian and some species of birds. We implemented a sero-epidemiological study in Isiolo County, Kenya, to determine relative seroprevalences of CCHFV in humans, livestock and in wild animals. In addition, we identified subject and environment level factors that could promote exposure to CCHFV. Humans (n = 580) and livestock (n = 2,137) were recruited into the study through a multistage random sampling technique, and in addition, various species of wild animals (n = 87) were also sampled conveniently. Serum samples from all recruited humans and animals were collected and screened for CCHFV antibodies using ID Screen multispecies, double-antigen IgG enzyme-linked immunosorbent assay (ELISA). The overall anti-CCHFV IgG seroprevalences in humans, cattle, goats, sheep and camels were 7.2% [95% CI: 3.1-15.8%], 53.9% [95% CI: 30.7-50.9%], 11.6% [95% CI: 7.2-22.5%], 8.6% [95% CI: 3-14%] and 89.7% [95% CI: 78-94%], respectively. On average, the sampled wild animals had CCHFV seroprevalence of 41.0% [95% CI: 29.1-49.4%]; giraffes had the highest mean CCHF seroprevalence followed by buffaloes, while impala had very low exposure levels. Statistical analyses using mixed effects logistic regression models showed that CCHFV exposure in humans was significantly associated with male gender, being over 30 years of age and belonging to a household with a seropositive herd. In livestock, a combination of animal- and environment level factors including older animals, being in an area with high normalized difference vegetation index (NDVI) and high vapour pressure deficit were significantly associated with CCHFV infection. Age, sex and species of wild animals were considered as the key risk factors in the analysis, but none of these variables was significant (P-value = 0.891, 0.401 and 0.664, respectively). Additionally, RT-qPCR analysis revealed the presence of CCHFV RNA in camels (30%), cattle (14.3%), and goats (3.8%), but not in humans, sheep, or wild animals. This study demonstrates that environmental factors, such as NDVI and vapor pressure deficit, affect CCHFV exposure in livestock, while the presence of infected livestock is the key determinant of human exposure at the household level. These findings underscore the importance of using One Health approaches to control the disease in human-livestock-wildlife interfaces. For instance, the existing CCHF surveillance measures could be enhanced by incorporating algorithms that simulate disease risk based on the environmental factors identified in the study. Additionally, tick control in livestock, such as the use of acaricides, could reduce CCHFV exposure in livestock and, consequently, in humans.

Preparation and characterisation of sodium chloride-doped CaO-Al2O3-SiO2 system glass-ceramics

ABSTRACT It is known that the treatments of chlorine-containing wastes, such as municipal solid waste incineration fly ash are particularly challenging. One method for treating chloride is to entrap it in glass by melting. It has been demonstrated that CaCl2 can be retained in CAS system glass-ceramics. However, as the main chloride, NaCl exhibits a low boiling point and a high vapour pressure. The fixation of NaCl and its effect on glass-ceramics remain unclear. In this study, 2.17% Cl− was incorporated into the base glass by limiting NaCl volatilisation during melting. Glass-ceramics were successfully prepared using the Cl-containing glass powder as the raw material by sintering and the chloride was evenly distributed between the glass phase and crystalline phase. The primary crystal phases observed were wollastonite and anorthite. Furthermore, when the sample was sintered at 825 °C for 4 hours, it exhibited a bending strength of 155 MPa and a hardness of 6.29 GPa. This method can effectively address the resourceful treatment of chlorine-containing wastes.

Triadic Halobenzene Processing Additive Combined Advantages of Both Solvent and Solid Types for Efficient and Stable Organic Solar Cells.

Solvent additives with a high boiling point (BP) and low vapor pressure (VP) have formed a key handle for improving the performance of organic solar cells (OSCs). However, it is not always clear whether they remain in the active-layer film after deposition, which can negatively affect the reproducibility and stability of OSCs. In this study, an easily removable solvent additive (4-chloro-2-fluoroiodobenzene (CFIB)) with a low BP and high VP is introduced, behaving like volatile solid additives that can be completely removed during the device fabrication process. In-depth studies of CFIB addition into the D18-Cl donor and N3 acceptor validate its dominant non-covalent intermolecular interactions with N3 through effective electrostatic interactions. Such phenomena improve charge dynamics and kinetics by optimizing the morphology, leading to enhanced performance of D18-Cl:N3-based devices with a power conversion efficiency of 18.54%. The CFIB-treated device exhibits exceptional thermal stability (T80 lifetime = 120h) at 85°C compared with the CFIB-free device, because of its morphological robustness by evolving no residual CFIB in the film. The CFIB features a combination of advantages of solvent (easy application) and solid (high volatility) additives, demonstrating its great potential use in the commercial mass production of OSCs.

Effect of hydrogen on oxidative dissolution of epsilon particles-doped UO2 pellets under carbonate condition with hydrogen peroxide

The epsilon particles that result from nuclear fission of UO2 fuel possess both advantages and disadvantages from a spent nuclear fuel (SNF) management perspective. In this study, the effect of epsilon particles, namely Ru, Mo, and Pd, inherent in simulated UO2 pellets is examined. Various analytical methods have been used to explore the changes in the structural, surface, and electrochemical properties of which contain epsilon particles. A notable finding is that the epsilon particles are not evenly distributed and tend to clump together, transforming into a metallic state after sintering, as detailed in the X-ray diffraction analyses. Energy-dispersive X-ray spectroscopy analyses highlight interesting aspects of the distribution of elements, especially the disappearance of Pd during sintering, which is likely due to its high vapor pressure. Although the lattice structure of UO2 remains unchanged, the sizes of the grains and pores visibly change, which may influence the tendency of UO2 pellet-cracking. Despite the addition of the epsilon particles, the electrical conductivity analyses show no significant changes, suggesting that they act as minor impurities without affecting the structural lattice. However, their possible role as catalysts in electrochemical reactions opens new and interesting areas that require thorough investigation. Moreover, examining the anodic dissolution under various conditions provides detailed insights into UO2 dissolution and oxidation, revealing how epsilon particles subtly influence the oxidative dissolution process. This study clarifies the basic interactions and effects of epsilon particles in UO2 pellets and broadens the path for a deeper understanding and improvement of nuclear fuel matrices and steering advancements in the safe and effective use of nuclear energy.