Theoretical Potential Research Articles

How Ir‐Rh Alloys Improve Electrochemical Ammonia Oxidation Activity Studied by Density Functional Theory

The electrochemical ammonia oxidation reaction (AOR) has applications in hydrogen storage and ammonia waste remediation. Using density functional theory, we investigate the mechanism of AOR on Ir, Rh, and their alloys at varied atomic ratios (Ir75Rh25, Ir50Rh50, and Ir25Rh75) towards N2(g), NO2–(aq), and NO3–(aq) formation. This work introduces a method for computational alloy design by considering both electronic energy and configurational entropy. The structures considered are selective to N2(g) formation and all favoured *N‐N coupling. An Ir50Rh50 alloy was found to reduce the theoretical onset potential for N2(g) formation relative to pure Ir while not exhibiting a downhill coupling step corresponding to catalyst poisoning by *N as shown for pure Rh, consistent with previous experimental work. The formation of NO2–(aq) and NO3–(aq) demand significantly higher potentials, typically limited by the final hydroxylation step before desorption.

3D NiCoW Metallic Compound Nano-Network Structure Catalytic Material for Urea Oxidation

Urea shows promise as an alternative substrate to water oxidation in electrolyzers, and replacing OER with the Urea Oxidation Reaction (UOR, theoretical potential of 0.37 V vs. RHE) can significantly increase hydrogen production efficiency. Additionally, the decomposition of urea can help reduce environmental pollution. This paper improves the inherent activity of catalytic materials through morphology and electronic modulation by incorporating tungsten (W), which accelerates electron transfer, enhances the electronic structure of neighboring atoms to create a synergistic effect, and regulates the adsorption process of active sites and intermediates. NiCoW catalytic materials with an ultra-thin nanosheet structure were prepared using an ultrasonic-assisted NaBH4 reduction method. The results show that during the OER process, NiCoW catalytic materials have a potential of only 1.53 V at a current density of 10 mA/cm2, while the UOR process under the same conditions requires a lower potential of 1.31 V, demonstrating superior catalytic performance. In a mixed electrolyte of 1 M KOH and 0.5 M urea, overall water splitting also shows excellent performance. Therefore, the designed NiCoW electrocatalyst, with its high catalytic activity, provides valuable insights for enhancing the efficiency of water electrolysis for hydrogen production and holds practical research significance.

Theoretical Assessment of Agro-Waste for Biogas Production Based on Novel Methodology Related to Biochemical Potential

Agricultural and waste biomasses present viable solutions for utilization in the energy sector, achieving sustainable and long-term transformation into energy and fuel. However, it is important to carefully evaluate the competing applications for these feedstocks, considering both short- and long-term stability. Biomass for biogas production in agriculture and waste management is used due to its availability and ease of handling. Considering everything mentioned, evaluating the most suitable raw materials for biogas production is crucial for meeting sustainability criteria and promoting biomass as an energy source. In this paper, an examination of different biomass sources as possible feedstock to produce biogas by applying a theoretical approach to the proximate and final analysis results of those materials is presented. Based on data from the raw material analysis, the theoretical biochemical methane potential (TBMP) for the considered samples was calculated. Furthermore, the mass and energy balance for the case study biogas plant was also performed. According to the obtained results, the considered feedstocks show the validity of their use for biogas production considering the fulfillment of the raw material minimum quantity, mandatory residue arrangement, and achieving higher efficiency of the energy conversion process.

“Dead Lithium” Formation and Mitigation Strategies in Anode‐Free Li‐Metal Batteries

AbstractThin lithium‐metal foil is a promising anode material for next‐generation batteries due to its high theoretical specific capacity and low negative potential. However, safety issues linked to dendrite growth, low‐capacity retention, and short cycle life pose significant challenges. Also, it has excess energy that must be minimized in order to reduce the battery costs. To limit excess lithium, practical lithium metal batteries need a negative‐to‐positive electrode ratio as close to 1 : 1 as possible, which can be achieved through limiting excess lithium or using an “anode‐free” metal battery design. However, both designs experience fast capacity fade due to the irreversible loss of active lithium in the cell, caused by the formation of the solid electrolyte interphase (SEI), dendrite formation and “dead lithium,” – refers to lithium that has lost its electronic connection to the anode electrode or current collector. The presence of dead lithium in batteries negatively affects their capacity and lifespan, while also raising internal resistance and generating heat. Additionally, dead lithium encourages the growth of lithium dendrites, which poses significant safety hazards. Within this fundamental review, we thoroughly address the phenomenon of dead lithium formation, assessing its origins, implications on battery performance, and possible strategies for mitigation. The transition towards environmentally friendly and high‐performance metal batteries could be accelerated by effectively tackling the challenge posed by dead lithium.

Investigation of a Single Atom Iron Catalyst for the Electrocatalytic Reduction of Nitric Oxide to Hydroxylamine: A DFT Study.

Hydroxylamine, as an important reducing agent, disinfectant, foaming agent, and biocide, plays a role in both human life and industrial production. However, its synthesis is confronted with challenges, such as high pollution and large consumption. Here, we propose a coordination tailoring strategy to design 47 graphene-supported single iron atom catalysts (SACs), namely, Fe@CxZy (Z = B, N, O, P, and S), for the reduction of nitric oxide to hydroxylamine. Using density functional theory calculations, we demonstrated the great impact of the coordination environment on the stability, catalytic selectivity, and activity of the Fe site. We identified that the experimentally available Fe@N4 possesses an ultralow theoretical limiting potential of -0.32 V compared to that of other catalysts. A comprehensive investigation of the electronic properties elucidates the underlying active origin and reaction mechanism of the nitric oxide reduction reaction to hydroxylamine on Fe@N4. These results not only explain the catalytic origin of synthesized SACs for the NH2OH production but also offer theoretical guidance for further optimizing high-performance catalysts.

Axial Coordination Engineering on Fe-N-C Materials for Oxygen Reduction: Insights from Theory.

Axial coordination engineering has emerged as an effective strategy to regulate the catalytic performance of metal-N-C materials for oxygen reduction reaction (ORR). However, the ORR mechanism and activity changes of their active centers modified by axial ligands are still unclear. Here, a comprehensive investigation of the ORR on a series of FeN4-L moieties (L stands for an axial ligand) is performed using advanced density functional theory (DFT) calculations. The axial ligand has a substantial effect on the electronic structure and catalytic activity of the FeN4 center. Specially, FeN4-C6H5 is screened as a promising active moiety with superior ORR activity, as further revealed by constant-potential calculations and kinetic analysis. The enhanced activity is attributed to the weakened *OH adsorption caused by the altered electronic structure. Moreover, microkinetic modeling shows that at pH=1, FeN4-C6H5 possesses an impressive theoretical half-wave potential of ~1.01 V, superior to the pristine Fe-N-C catalysts (~0.88 V) calculated at the same level. These findings advance the understanding of the ORR mechanism of FeN4-L and provide guidance for optimizing the ORR performance of single-metal-atom catalysts.

Evaluation of Biochemical Methane Potential and Kinetics of Organic Waste Streams for Enhanced Biogas Production

Organic waste has the potential to produce methane gas as a substitute for petrol-based fuels, while reducing landfilling and possible environmental pollution. Generally, anaerobic digestion (AD) is used only in wastewater treatment plants as a tertiary stage of sewage sludge treatment, generating a fraction of the energy that such process plants require. In this study, four different wastes—food waste (FW), dairy industry waste (DIW), brewery waste (BW), and cardboard waste (CBW)—were tested for biogas production. The biochemical methane potential (BMP) of each sample was evaluated using an automatic methane potential system (AMPTS). Operating parameters such as pH, temperature, total solids, and volatile solids were measured. Experiments on the anaerobic digestion of the samples were monitored under mesophilic conditions (temperature 37 °C, retention time 30 days). Specific methane yields (SMYs), as well as the theoretical methane potential (BMPth), were used to calculate the biodegradability of the substrates, obtaining the highest biodegradability for BW at 95.1% and producing 462.3 ± 1.25 NmL CH4/g volatile solids (VS), followed by FW at an inoculum-to-substrate ratio (ISR) of 2 at 84% generating 391.3 NmLCH4/g VS. The BMP test of the dairy industry waste at an inoculum-to-substrate ratio of 1 was heavily inhibited by bacteria overloading of the easily degradable organic matter, obtaining a total methane production of 106.3 NmL CH4/g VS and a biodegradability index of 24.8%. The kinetic modeling study demonstrated that the best-fitting model was the modified Gompertz model, presenting the highest coefficient of determination (R2) values, the lowest root means square error (RMSE) values for five of the substrates, and the best specific biogas yield estimation with a percentage difference ranging from 0.3 to 3.6%.

Analytical comparison of the boil-off gas recondensation process’s energy consumption and carbon emissions

With 28 operational liquefied natural gas receiving terminals in China by 2023, totaling a receiving capacity of 1.2 × 108 t/a, managing carbon emissions and boil-off gas has attracted increased attention. This study presents the optimization of 8 boil-off gas (BOG) recondensation processes, considering energy consumption and carbon emissions as assessment criteria, along with two types of vaporizers. The method involves analyzing how process parameters affect system performance using Hydraulic System Simulation Software, followed by optimizing system parameters with a genetic algorithm. It explores the impact of compressor output pressure, after-cooler inlet material ratio, and pre-cooler inlet material ratio on system energy consumption and carbon emissions. Results show that increased recondensing, compression, and cooling measures slightly elevate energy consumption but significantly reduce carbon emissions. Moreover, a higher BOG content enhances the carbon reduction effect. This study represents the first optimization of BOG recondensation processes focusing on carbon emissions, offering fresh theoretical insights and significant potential for enhancing energy efficiency and reducing carbon emissions.

Photovoltaic-powered seasonal snow storage-assisted district cooling system: Site suitability analysis and performance assessment

District cooling (DC) plants coupled with cold thermal energy storage (TES) and photovoltaic (PV) systems are getting attention worldwide. Utilising winter snow is a successfully implemented TES technology, with little scale-up. Its site identification and cooling potential are not yet fully explored, especially for DC applications. The objective of this paper is to carry out site suitability analysis and performance assessment for PV-powered snow storage-assisted DC system. The site selection methodology is based on multi-criteria decision-making techniques and geographic information system. Performance analysis is carried out mathematically by considering ten indicators. The robustness of the study is enhanced by multiple sensitivity analysis. For the base case scenario, the dominant selection criteria are observed to be cooling load density (30 %), proximity to electric grids (17 %) and air temperature (13 %). Out of the selected land cover (vacant/crops/rangeland) in Estonia, around 34 km2 was observed to be moderately-suitable for the development of the proposed system. For a specific site, the theoretical generation potential of snow cooling facility is estimated as 1728 MWh with an annual cooling share of 80 %. With annual energy output of 1823 MWh and performance-ratio of 78 %, rooftop PV plants is capable to fully power the proposed system. A satisfactory economic and environmental performance is observed at the whole system level. This study is expected to scientifically support the effective utilisation of locally available energy sources (i.e. winter snow and solar energy) for space cooling applications in cold regions.

Oxygen Reduction Reaction Coupled Electro‐Oxidation for Highly‐Efficient and Sustainable Water Treatment

AbstractElectro‐oxidation (EO) technology demonstrates significant potential in wastewater treatment. However, the high energy consumption has become a pivotal constraint hindering its large‐scale implementation. Herein, we design an EO and 4‐electron oxygen reduction reaction coupled system (EO‐4eORR) to replace the traditional EO and hydrogen evolution reaction (HER) coupled system (EO‐HER). The theoretical cathodic potential of the electrolytic reactor is tuned from 0 V (vs. RHE) in HER to 1.23 V (vs. RHE) in 4eORR, which greatly decreases the required operation voltage of the reactor. Moreover, we demonstrate that convection can improve the mass transfer of oxygen and organic pollutants in the reaction system, leading to low cathodic polarization and high pollutant removal rate. Compared with traditional EO‐HER system, the energy consumption of the EO‐4eORR system under air aeration for 95 % total organic carbon (TOC) removal is greatly decreased to 2.61 kWh/kgTOC (only consider the electrolyzer energy consumption), which is superior to previously reported EO‐based water treatment systems. The reported results in this study offer a new technical mode for development of highly efficient and sustainable EO‐based treatment systems to remove organic pollutants in waste water.

Oxygen Reduction Reaction Coupled Electro-Oxidation for Highly-Efficient and Sustainable Water Treatment.

Electro-oxidation (EO) technology demonstrates significant potential in wastewater treatment. However, the high energy consumption has become a pivotal constraint hindering its large-scale implementation. Herein, we design an EO and 4-electron oxygen reduction reaction coupled system (EO-4eORR) to replace the traditional EO and hydrogen evolution reaction (HER) coupled system (EO-HER). The theoretical cathodic potential of the electrolytic reactor is tuned from 0 V (vs. RHE) in HER to 1.23 V (vs. RHE) in 4eORR, which greatly decreases the required operation voltage of the reactor. Moreover, we demonstrate that convection can improve the mass transfer of oxygen and organic pollutants in the reaction system, leading to low cathodic polarization and high pollutant removal rate. Compared with traditional EO-HER system, the energy consumption of the EO-4eORR system under air aeration for 95 % total organic carbon (TOC) removal is greatly decreased to 2.61 kWh/kgTOC (only consider the electrolyzer energy consumption), which is superior to previously reported EO-based water treatment systems. The reported results in this study offer a new technical mode for development of highly efficient and sustainable EO-based treatment systems to remove organic pollutants in waste water.

Harnessing the power of ChatGPT to promote Construction Hazard Prevention through Design (CHPtD)

PurposeConstruction Hazard Prevention through Design (CHPtD) is recognized as a pivotal strategy for enhancing workplace safety. Despite its theoretical potential, practical implementation faces challenges, particularly regarding designers' familiarity with field-level operations and hazard recognition. This study aims to investigate whether ChatGPT can address these challenges by assisting in hazard recognition during CHPtD sessions.Design/methodology/approachThe research utilized a randomized controlled experiment to assess ChatGPT as an intervention in supporting hazard recognition during CHPtD sessions. The study involves 162 civil and construction engineering student participants, representing future professionals. Participants engaged in hazard recognition during CHPtD sessions either with or without the assistance of ChatGPT.FindingsParticipants who utilized ChatGPT during CHPtD sessions demonstrated a significant improvement in hazard recognition, identifying approximately 40% more hazards compared to those who did not use ChatGPT. These findings underscore the efficacy of ChatGPT in supporting CHPtD efforts.Practical implicationsThe results highlight the practical utility of harnessing ChatGPT in CHPtD sessions to enhance hazard recognition and ultimately promote workplace safety. By leveraging ChatGPT, designers and engineers can better anticipate and mitigate potential hazards during the design phase, thus creating a safer working environment for field workers.Originality/valueThis research contributes to addressing the challenges associated with implementing CHPtD by introducing ChatGPT as a valuable tool to support hazard recognition. By demonstrating the effectiveness of ChatGPT in enhancing hazard identification during CHPtD sessions, this study offers a novel approach to promoting the adoption of CHPtD and advancing workplace safety initiatives.

Farmers’ willingness to introduce short-rotation tree plantations on agricultural land: A case study in southern Sweden

To meet climate targets, expanding Populus spp. tree cultivation is proposed as a potential biomass feedstock, especially on agricultural land that does not come into conflict with food production. However, biomass potential assessments typically overlook landowners' perspectives, risking a gap between theoretical potentials and realisation. Here, we test empirical consequences of two hypotheses based on a survey targeting southern Swedish farmers: 1) Relying exclusively on agricultural land cover data to identify abandoned agricultural land leads to an overestimation of the total agricultural land that can be utilised for future biomass production from Populus spp. feedstocks. 2) The absence of data on farmers' intentions to cultivate fast-growing tree species on agricultural land leads to overestimation of the potential biomass supply from Populus spp. in biomass assessments. Findings suggest that less than 50 % of farmers with unsubsidised arable land, which is often assumed to be abandoned, would consider cultivating these tree species on this type of land (26 % [7–48]). Furthermore, only 11 % [6–17] would consider cultivating Populus spp. on agricultural land overall during 2021–2030, indicating a generally low level of interest among farmers. However, higher rates were observed in forested areas. The projected near-future cultivation potential of 2.0 kha [1.1–3.0] suggests an at least threefold overestimation in previous theoretical assessments. This study highlights a disparity between biophysical land data and producer perspectives, showing that neglecting farmers’ perspectives risks overestimating the biomass supply, potentially leading to misguided expectations and inefficient policies. Our findings support targeted policy recommendations.

Empowering Tri-Functional Palladium's Catalytic Activity and Durability in Electrocatalytic Formic Acid Oxidation Reaction via Innovative Self-Caging and Alloying Strategies.

Direct formic acid fuel cells (DFAFCs) stand out for portable electronic devices owing to their ease of handling, abundant fuel availability, and high theoretical open circuit potential. However, the practical application of DFAFCs is hindered by the unsatisfactory performance of electrocatalysts for the sluggish anodic formic acid oxidation reaction (FAOR). Palladium (Pd) based nanomaterials have shown promise for FAOR due to their highly selective reaction mechanism, but maintaining high electrocatalytic durability remains challenging. In this study, a novel Pd-based electrocatalyst (UiO-Pd-E) is reported with exceptional durability and activity for FAOR, which can be attributed to the Pd nanoparticles encapsulated within a carbon framework where concurrent chemical alloying of Pd and Zr occurs. Further, the UiO-Pd-E demonstrates noteworthy multifunctionality in various electrochemical reactions including electrocatalytic ethanol oxidation reaction (EOR) and oxygen reduction reaction (ORR) in addition to the FAOR, highlighting its practical potentials.

Biochar mitigation potential in Norway estimated by IPCC Tier 1 and Tier 2 methods

Biochar is a recalcitrant carbon-rich solid produced by pyrolysis of organic residues, and its application to soil is considered a promising approach to mitigate climate change, as biochar resists decomposition to readily contributes to soil carbon (C) sequestration. The IPCC provides a basis for future national-scale accounting of the changes in soil C stocks following biochar application to cropland soils. The IPCC Tier 1 approach for biochar is based on fixed emission factors to estimate biochar C sequestration. In contrast, the Tier 2 approach allows countries to use local emission factors and climate data to calculate the contribution of biochar to soil C sequestration. Accurate accounting of biochar C sequestration is essential for ensuring the credibility of C offsetting projects, as well as providing incentives for implementing biochar in C credit schemes, calling for comparative analyses of the different biochar Tier approaches. Here we retrieved biochar samples from local producers and measured their H/Corg to estimate the persistence of biochar in Norwegian croplands post application. Various feedstocks were considered, including forest residues, woody wastes, manure, sludge, and straw. For all biochar samples, the 100-year stable C fraction was calculated at ≥ 0.945, thus exceeding the default Tier 1 value (0.8). Biochar sourced from woody- and forestry residues had a Corg content above the default Tier 1 value (0.77). Based on this and data about national feedstock supplies, we compared the theoretical potential of biochar soil C sequestration to mitigate climate change in Norway, using the IPCC Tier 1 and Tier 2 approaches. Biochar C sequestration in soil was calculated at 0.79 Tg CO2-eq yr−1 and 0.92 to 0.96 Tg CO2-eq yr−1, respectively for the Tier 1 and Tier 2 approaches, thus, underlining that the choice of IPCC Tier approach can have a large impact on the estimated mitigation potential of biochar.

Bi-Functional Interfacial Modification enables Highly-Exposed Zn(002) Crystal Facet towards Durable Zn Metal Batteries.

Zn-ion batteries (ZIBs) have garnered growing interest in large-scale energy storage devices for the high safety, high theoretical capacity and low electrochemical potential. Nevertheless, their widespread applications are significantly impeded by dendrite formation, hydrogen evolution and corrosion reactions of Zn anodes. Herein, a bi-functional polyacrylic acid (PAA) modified-Zn anode (Zn-PAA) is designed to concurrently inhibit Zn dendrite formation and alleviate side reactions. The bi-functional PAA coating not only selectively acid-etches the active Zn crystal facets to guide the planar deposition along the highly-exposed Zn(002) crystal facet, but also facilitate uniform Zn deposition through coordination between the polymer functional groups and Zn2+. Meanwhile, the electrically-insulated PAA protective layer effectively separates Zn anodes from the electrolyte and modulates the solvation structure of Zn2+.6H2O, significantly suppressing side reactions. Consequently, the assembled Zn-PAA//Zn-PAA symmetrical cell delivers an outstanding cycling stability of 1600 h at 1 mA cm-2 and 1 mAh cm-2. The assembled KVO//Zn-PAA full cell shows exceptional cycling stability over 1500 cycles at 2.0 A g-1 with a high Coulombic efficiency approaching 100%. The facile bi-functional surface modification strategy, which enables to finely tune the crystal facet texture and ion distribution manner, opens up a groundbreaking path towards safe and durable ZIBs.

Interfacial Acid‐Like Microenvironment and Orbital Modulating Strategy toward Efficient Hydrogen Evolution in Neutral High‐Salinity Wastewater/Seawater

Electrochemical high‐salinity wastewater splitting is a promising technology for green hydrogen (H2) production. However, the kinetics of hydrogen evolution reaction (HER) in neutral media is slow, and the high theoretical potential of oxygen evolution reaction leads to large energy losses. Herein, an iron‐based electrocoagulation‐coupled hydrogen production integrated system (IEHPS) is constructed, which is realized by coupling low‐potential anodic iron oxidation reaction with cathodic HER. The non‐noble metal HxWO3‐Ni catalyst is synthesized by fabricating a proton sponge HxWO3 to achieve an interfacial acid‐like microenvironment and doping it with Ni heteroatom to modulate the 4d orbital of W, thereby weakening the adsorption strength of the W site toward hydrogen. Consequently, the HxWO3 Ni demonstrates remarkable performance characteristics, boasting a mere 131 mV overpotential at 10 mA cm−2 and Tafel slope of 44 mV dec− in neutral media. Operating at an applied voltage of 1.5 V, the IEHPS exhibits a high hydrogen production rate of 235 mL g−1 min−1 in seawater. It achieves nearly complete removal of contaminants like rhodamine B and heavy metal ions within a rapid 8–20 min, with an energy consumption of only 3.7 kWh Nm−3. This study provides a promising pathway for efficient and energy‐saving production of high‐purity hydrogen and effective treatment of high‐salinity wastewater.

Closing the Loop between Plastic Waste Management and Energy Cogeneration: An Innovative Design for a Flexible Pyrolysis Small-Scale Unit

This study proposes a simplified unit that can be employed in an industrial facility for the utilization of its own abundant plastic waste, primarily from discarded packaging, to achieve full or partial energy autonomy. By converting this waste into synthetic pyrolysis oil equivalent to 91,500 L, the industry can power a combined heat and power generation unit. The proposed unit was designed with a focus on maintaining high temperatures efficiently while minimizing oxygen exposure to protect the integrity of hydrocarbons until they transform into new compounds. Pyrolysis stands as a foundational procedure, paving the way for subsequent thermochemical transformations such as combustion and gasification. This study delves into the factors affecting pyrolysis and presents analytically the mathematical formulations and relevant calculations in order to effectively design and apply a real-life system. On this basis, fuels from plastic waste can be produced, suitable for utilization in typical equipment meant to produce heat, estimated for six months’ operation and 800 MWh of electricity. This study enhances the transition towards a more circular and resource-efficient economy with technologies that unlock the latent energy contained within the discarded matter. Additionally, it demonstrates the feasibility of a moderate investment in a co-generation system for industries utilizing 568 tonnes of plastic waste per year. The design and accurate calculations of this study highlight the theoretical potential of this technology, promoting environmental sustainability and resource conservation.

Electrodeposited zinc cobalt bimetallic phosphate as a bifunctional catalyst for hydrogen evolution and urea oxidation

The theoretical potential of the urea oxidation reaction (UOR) is a mere 0.37 V(vs.RHE), significantly lower than the 1.23 V (vs. RHE) of the oxygen evolution reaction (OER). Thus, substituting the OER with the UOR can effectively reduce the voltage required for electrolysis. Transition metal phosphates (TM-Pi), with their unique physical properties, can partly replace precious metal catalysts and hold great application potential. However, further modification is necessary to enhance their catalytic activity and stability. Therefore, this study prepared a coral-like cluster Co/Zn-Pi@NF (Pi represents phosphate) catalyst, which was grown in situ on nickel foam (NF) using the constant current electrodeposition method. The catalyst exhibited superior catalytic performance in 1 M KOH, with the required overpotentials for the hydrogen evolution reaction (HER) and OER reaching 10 mA·cm−2 being 36.6 mV and 343.4 mV, respectively. In 1 M KOH containing 0.5 M urea, the urea oxidation potential was only 1.4 V, which remained stable for 60 hours. The Co/Zn-Pi@NF nanoparticles were used as the anode and cathode for water-urea electrolysis, and the electrolysis voltage was 1.43 V at a current density of 10 mA·cm−2, which was 290 mV lower than that of electrolyzed water. This study demonstrates that zinc-cobalt bimetallic phosphate can be used as a dual-function electrocatalyst for hydrogen evolution and urea oxidation.

Harmonization potential of the fragmented farmlands in Finland: The pros and cons for critical parcel characteristics

Agricultural landscapes have been shaped by gradual, partially optimized changes in farms and surrounding areas which have resulted in fragmented agricultural landownership and increased distances on farms. Since Finland joined the EU in 1995, the average farm size has more than doubled which has increased the distances on farms. This may have caused trade-offs with resource use efficiency, productivity, and sustainability. The aim of this study was to evaluate the potential and impacts of land reallocation by integrating regional variability, logistical factors, and emerging satellite imagery, with an emphasis on enhancing resilience in future climates. This study estimated the theoretical potential for land reallocation between farms to reduce farmland fragmentation but also applied fixed land exchange rates (5 % to 40 %) with the primary aim to reduce distances within each farm depending on the farm size and region. The aim was also to identify co-benefits and trade-offs on the number of parcels in a farm, the production capacity of exchanged parcels, diversification potential, and the proximity of parcels to waterways. While keeping the farm size constant, large potential was found to optimize fragmented landscapes and reduce distances within farms especially on large farms. However, only a moderate exchange rate of 5 % almost halved the distances in the best cases of the farms, while exchange rates >20 % provided less additional logistic benefits. Thereby, modest, well targeted measures are not only more acceptable to landowners but may provide the most benefits with fewer trade-offs. In unsatisfactory cases, large parcels were replaced by higher numbers of smaller ones, productivity differences occurred, and closer parcels became more uniform, which may reduce diversification options, which are important for resilience and sustainability. Hence, merging and reshaping nearby parcels after reallocation might be needed to complete rationalization. Estimated changes in the proximity of the parcels to waterways tended to improve the farmers’ readiness to implement irrigation as an adaptation measure to climate change. The variable outcome of parcel reallocation emphasizes the central role of the current customer-driven consolidation system chaired by independent land surveyors to boost the land reallocation also in the future to improve logistics, resource efficiency, and sustainability on farms that today struggle with cost-crises.