High Energy Research Articles

TSO-DSO interface for Net Zero: the German case of 50Hertz and its DSO neighbour TEN Thüringer Energienetz*

As Germany advances towards its energy transition goals, the imperative to expand and restructure its power grid infrastructure becomes increasingly evident. The current infrastructure lacks the capacity to meet future demands, highlighting the pressing need for action. Escalating challenges related to system security and grid reliability underscore the critical importance of fostering close coordination between Distribution System Operators (DSOs) and Transmission System Operators (TSOs). Collaboration is particularly crucial in control areas such as for instance 50Hertz’s in north-eastern Germany, where efficient management of energy fluctuations is essential for the successful transition to high renewable energy usage. Regulatory strategies aimed at facilitating this transition must prioritize a strong collaboration between DSOs and TSOs necessary for stability, optimizing operations, and securing the network. This article is intended to illustrate how a regulatory framework for such TSO-DSO cooperation in north-eastern and eastern Germany for congestion management could be necessary, in accordance with the next grid development plans. Regulatory gaps associated with such interface will be identified and policy recommendations derived from them will address the challenges and opportunities linked to congestion management and the utilization of smart grid technologies.

Optimizing high-temperature energy storage in tungsten bronze-structured ceramics via high-entropy strategy and bandgap engineering

As a vital material utilized in energy storage capacitors, dielectric ceramics have widespread applications in high-power pulse devices. However, the development of dielectric ceramics with both high energy density and efficiency at high temperatures poses a significant challenge. In this study, we employ high-entropy strategy and band gap engineering to enhance the energy storage performance in tetragonal tungsten bronze-structured dielectric ceramics. The high-entropy strategy fosters cation disorder and disrupts long-range ordering, consequently regulating relaxation behavior. Simultaneously, the reduction in grain size, elevation of conductivity activation energy, and increase in band gap collectively bolster the breakdown electric strength. This cascade effect results in outstanding energy storage performance, ultimately achieving a recoverable energy density of 8.9 J cm−3 and an efficiency of 93% in Ba0.4Sr0.3Ca0.3Nb1.7Ta0.3O6 ceramics, which also exhibit superior temperature stability across a broad temperature range up to 180 °C and excellent cycling reliability up to 105. This research presents an effective method for designing tetragonal tungsten bronze dielectric ceramics with ultra-high comprehensive energy storage performance.

Exceptional Rate Performances of Li-Rich Mn-Based Cathodes Enabled by Boron-Based Additives-Driven Self-Optimized Interface.

Li-rich Mn-based cathode material (LRM), as a promising cathode for high energy density lithium batteries, suffers from severe side reactions in conventional lithium hexafluorophosphate (LiPF6)-based carbonate electrolytes, leading to unstable interfaces and poor rate performances. Herein, a boron-based additives-driven self-optimized interface strategy is presented to dissolve low ionic conductivity LiF nanoparticles at the outer cathode electrolyte interface, leading to the optimized interfacial components, as well as the enhanced Li ion migration rate in electrolytes. Being attributed to these superiorities, the LRM||Li battery delivers a high-capacity retention of 92.19% at 1C after 200 cycles and a low voltage decay of 1.08 mV/cycle. This work provides a new perspective on the rational selection of functional additives with an interfacial self-optimized characteristic to achieve a long lifespan LRM with exceptional rate performances.

Partitioning polar-slush strategy in relaxors leads to large energy-storage capability.

Relaxor ferroelectric (RFE) films are promising energy-storage candidates for miniaturizing high-power electronic systems, which is credited to their high energy density (Ue) and efficiency. However, advancing their Ue beyond 200 joules per cubic centimeter is challenging, limiting their potential for next-generation energy-storage devices. We implemented a partitioning polar-slush strategy in RFEs to push the boundary of Ue. Guided by phase-field simulations, we designed and fabricated high-performance Bi(Mg0.5Ti0.5)O3-SrTiO3-based RFE films with isolated slush-like polar clusters, which were realized through suppression of the nonpolar cubic matrix and introduction of highly insulating networks. The simultaneous enhancement of the reversible polarization and breakdown strength leads to a Ue of 202 joules per cubic centimeter with a high efficiency of ~79%. The proposed strategy provides a design freedom for next-generation high-performance dielectrics.

Surface Coating of NCM523 Cathode Electrodes by the Difunctional Block Copolymer/Lithium Salt Composites.

Nickel-rich layered oxide cathodes, such as LiNi0.5Co0.2Mn0.3O2 (NCM523), are prevalent in high-power batteries owing to their high energy density. However, these cathodes suffer from undesirable side reactions occurring at the cathode/liquid electrolyte interface, leading to inferior interface stability and poor cycle life. To address these issues, herein, an amphiphilic diblock copolymer poly(dimethylsiloxane)-block-poly(acrylic acid) (PDMS-b-PAA) along with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) is utilized for modifying the electrode surface. This modification causes a thin and stable cathode-electrolyte interface (CEI) on the surface of NCM523 particles, as evidenced by XPS, TEM, and EIS analysis. The introduction of this modified interface successfully suppresses the capacity fading of NCM523. After 200 cycles at a rate of 1.0 C, the capacity of the modified NCM523 cathode is 108.7 mAh g-1, with a capacity retention of 82.8%, while the control samples without the polymer modification display a capacity retention of 72.7%. These results outline the distinct advantage of electrode surface modification with diblock copolymers/LiTFSI for the stabilization of Ni-rich layered oxide cathodes.

Carbonate Ester-Based Sodium Metal Battery with High-Capacity Retention at -50°C Enabled by Weak Solvents and Electrodeposited Anode.

Sodium metal batteries (SMBs) have received increasing attention due to the abundant sodium resources and high energy density, but suffered from the sluggish interfacial kinetic and unstable plating/stripping of sodium anode at low temperature, especially when matched with ester electrolytes. Here, we develop a stable ultra-low-temperature SMBs with high-capacity retention at -50°C in a weak solvated carbonate ester-based electrolyte, combined with an electrodeposited Na (Cu/Na) anode. The Cu/Na anode with electrochemically activated "deposited sodium" and stable inorganic-rich solid electrolyte interphase (SEI) was favor for the fast Na+ migration, therefore accelerating the interfacial kinetic process. As a result, the Cu/Na || NaCrO2 battery exhibited the highest capacity retention (compared to room-temperature capacity) in carbonate ester-based SMBs (98.05% at -25°C, 91.3% at -40°C, 87.9% at -50°C, respectively). The cyclic stability of 350 cycles at -25°C with a high energy efficiency of 96.15% and 70 cycles at -50°C can be achieved. Even in chill atmospheric environment with the fluctuant temperature, the battery can still operate over one month. This work provides a new opportunity for the development of low-temperature carbonate ester-based SMBs.

Unlocking 4.9 V Quasi-Solid-State Lithium Metal Battery via Solvent Screening and Interfacial Manipulation.

Parlous structure integrity of the cathode and erratic interfacial microdynamics under high potential take responsibility for the degradation of solid-state lithium metal batteries (LMBs). Here, high-voltage LMBs have been operated by modulating the polymer electrolyte intrinsic structure through an intermediate dielectric constant solvent and further inducing the gradient solid-state electrolyte interphase. Benefiting from the chemical adsorption between trimethyl phosphate (TMP) and the cathode, the gradient interphase rich in LiPFxOy and LiF is induced, thereby ensuring the structural integrity and interface compatibility of the commercial LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode even at the 4.9 V cutoff voltage. Eventually, the specific capacity of NCM811|Li full cell based on TMP-modulated polymer electrolyte increased by 27.7% from 4.5 to 4.9 V. Such a universal screening method of electrolyte solvents and its derived electrode interfacial manipulation strategy opens fresh avenues for quasi-solid-state LMBs with high specific energy.

Optimization of Porous Structures of Carbon Matrices for Loading Red Phosphorus to Achieve High-Capacity and Long-Life Anodes for All-Solid-State Lithium-Ion Batteries.

All-solid-state lithium-ion batteries (ASSLIBs) using sulfide electrolytes and high-capacity alloy-type anodes have attracted sizable interest due to their potential excellent safety and high energy density. Encapsulating insulating red phosphorus (P) inside nanopores of a carbon matrix can adequately activate its electrochemical alloying reaction with lithium. Therefore, the porosity of the carbon matrix plays a crucial role in the electrochemical performance of the resulting red P/carbon composites. Here, we use zeolite-templated carbon (ZTC) with monodisperse micropores and mesoporous carbon (CMK-3) with uniform mesopores as the model hosts of red P. Our results reveal that micropores enable more effective pore utilization for the red P loading, and the P@ZTC material can achieve a record-high content (65.0 wt %) of red P confined within pores. When used as an anode of ASSLIBs, the P@ZTC electrode delivers an ultrahigh capacity of 1823 mA h g-1 and a high initial Coulombic efficiency of 87.44%. After 400 deep discharge-charge cycles (running over 250 days) at 0.2 A g-1, the P@ZTC electrode still holds a reversible capacity of 1260 mA h g-1 (99.92% capacity retention per cycle). Moreover, a P@ZTC||LiNi0.8Co0.1Mn0.1O2 full cell can deliver a reversible areal capacity of over 3 mA h cm-2 at 0.1C after 100 cycles.

Detection of Noncovalent Protein-Ligand Complexes by IR-MALDESI-MS.

Native mass spectrometry (MS) is a powerful analytical technique to directly probe noncovalent protein-protein and protein-ligand interactions. However, not every MS platform can preserve proteins in their native conformation due to high energy deposition from the utilized ionization source. Most small molecules approved as drugs and in development interact with their targets through noncovalent interactions. Therefore, rapid methods to analyze noncovalent protein-ligand interactions are necessary for the early stages of the drug discovery pipeline. Herein, we describe a method for analyzing noncovalent protein-ligand complexes by IR-MALDESI-MS with analysis times of ∼13 s per sample. Carbonic anhydrase and the kinase domain of Bruton's tyrosine kinase are paired with known noncovalent binders to evaluate the effectiveness of native MS by IR-MALDESI.

Constructing Sn-Cu2O Lithiophilicity Nanowires as Stable and High-Performance Lithium Metal Anodes.

Lithium (Li) metal batteries (LMBs) have garnered significant research attention due to their high energy density. However, uncontrolled Li dendrite growth and the continuous accumulation of "dead Li" directly lead to poor electrochemical performance in LMBs, along with serious safety hazards. These issues have severely hindered their commercialization. In this study, a lithiophilic layer of Sn-Cu2O is constructed on the surface of copper foam (CF) grown with Cu nanowire arrays (SCCF) through a combination of electrodeposition and plasma reduction. Sn-Cu2O, with excellent lithiophilicity, reduces the Li nucleation barrier and promotes uniform Li deposition. Simultaneously, the high surface area of the nanowires reduces the local current density, further suppressing the Li dendrite growth. Therefore, at 1 mA cm-2, the half cells and symmetric cells achieve high Coulombic efficiency (CE) and stable operation for over 410 cycles and run smoothly for more than 1350 h. The full cells using an LFP cathode demonstrate a capacity retention rate of 90.6% after 1000 cycles at 5 C, with a CE as high as 99.79%, suggesting excellent prospects for rapid charging and discharging and long-term cyclability. This study provides a strategy for modifying three-dimensional current collectors for Li metal anodes, offering insights into the construction of stable, safe, and fast-charging LMBs.

Modulating Surface Architecture and Electronic Conductivity of Li-rich Manganese-Based Cathode.

Li-rich manganese-based cathode (LRMC) has attracted intense attention to developing advanced lithium-ion batteries with high energy density. However, LRMC is still plagued by poor cyclic stability, undesired rate capacity, and irreversible oxygen release. To address these issues, herein, a feasible polyvinylidene fluoride (PVDF)-assisted interface modification strategy is proposed for modulating the surface architecture and electronic conductivity of LRMC by intruding the F-doped carbon coating, spinel structure, and oxygen vacancy on the LRMC, which can greatly enhance the cyclic stability and rate capacity, and restrain the oxygen release for LRMC. As a result, the modified material delivers satisfactory cyclic performance with a capacity retention of 90.22% after 200 cycles at 1C, an enhanced rate capacity of 153.58mAhg-1 at 5C and 126.32mAhg-1 at 10C, and an elevated initial Coulombic efficiency of 85.63%. Moreover, the thermal stability, electronic conductivity, and structure stability of LRMC are also significantly improved by the PVDF-assisted interface modification strategy. Therefore, the strategy of simultaneously modulating the surface architecture and the electronic conductivity of LRMC provides a valuable idea to improve the comprehensive electrochemical performance of LRMC, which offers a promising reference for designing LRMC with high electrochemical performance.

The U-Matrix geometrical model for multi-particle production in high-energy hadronic collisions

Inspired by the picture portraying the KNO scaling violation as an extension of the geometrical scaling violation, the current study proposes a phenomenological model for multi-particle production in hadron collisions based on the geometrical approach and using the U-Matrix unitarization scheme of the scattering amplitude. The model has been fine-tuned and all parameters have been derived from optimal fits to various hadronic multiplicity distributions data in p + pp¯\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ p\\left(\\overline{p}\\right) $$\\end{document} collisions across a broad range of energies. The results have revealed that our model furnishes a reasonable description of diverse multiplicity distributions at various energies. Besides, they have demonstrated a pronounced violation of the geometrical scaling, which eventually resulted in a significant violation of the KNO scaling. The study has also analyzed the higher-order moments of the multiplicity distribution. We have observed an unexpected overestimation of the fluctuations and correlations between final state particles with increasing energy, particularly above LHC energy. It is claimed that this overestimation is due to statistical fluctuations embedded in the U-matrix scheme. The findings of this study have shed light on the key role of the U-matrix scheme in the impact of collision geometry on multi-particle production processes at high energy.

The U-Matrix geometrical model for multi-particle production in high-energy hadronic collisions

Inspired by the picture portraying the KNO scaling violation as an extension of the geometrical scaling violation, the current study proposes a phenomenological model for multi-particle production in hadron collisions based on the geometrical approach and using the U-Matrix unitarization scheme of the scattering amplitude. The model has been fine-tuned and all parameters have been derived from optimal fits to various hadronic multiplicity distributions data in p + pp¯\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ p\\left(\\overline{p}\\right) $$\\end{document} collisions across a broad range of energies. The results have revealed that our model furnishes a reasonable description of diverse multiplicity distributions at various energies. Besides, they have demonstrated a pronounced violation of the geometrical scaling, which eventually resulted in a significant violation of the KNO scaling. The study has also analyzed the higher-order moments of the multiplicity distribution. We have observed an unexpected overestimation of the fluctuations and correlations between final state particles with increasing energy, particularly above LHC energy. It is claimed that this overestimation is due to statistical fluctuations embedded in the U-matrix scheme. The findings of this study have shed light on the key role of the U-matrix scheme in the impact of collision geometry on multi-particle production processes at high energy.

A novel formulation of wind velocity spectrum incorporating rainfall influence

Wind-rain interaction constitutes a common physical phenomenon in nature. Nevertheless, in fluid mechanics and wind engineering, whether and how rainfall influences wind remains an unresolved challenge. This study relies on a substantial dataset obtained through on-site measurement. Initially, three distinct rainfall categories—light rain, moderate rain, and heavy rain—are established based on the magnitude of vertical wind velocity. Notably, significant disparities in the high-frequency constituents of the fluctuating wind velocity spectrum are discerned across various rainfall levels. Subsequently, a rigorous quantitative analysis explores the relationship between the high-frequency cumulative energy proportion of the fluctuating wind velocity spectrum and rainfall intensity, leading to formulations that delineate the high-frequency cumulative energy proportion in the alongwind, acrosswind, and vertical wind directions as explicit functions of rainfall intensity. Moreover, a comprehensive unified expression models the three-dimensional fluctuating wind velocity spectrum. This expression incorporates parameters encompassing the relative scales of fluctuation and mean components, the extent of conversion between high and low-frequency energy, and the scaling laws governing the inertial subrange. Additionally, explicit functional dependencies for these parameters concerning variations in rainfall intensity are provided. The novel formulation of the fluctuating wind velocity spectrum proposed in this study bears substantial scientific significance, as it facilitates a deeper understanding of wind-rain interaction and offers valuable insights for conducting intricate environmental flow field simulations.

Thermal effects of organic porous media on absorption and desorption behaviors of carbon dioxide

As a result of global warming, people are increasingly concerned about greenhouse gas emissions, particularly carbon dioxide (CO2). Many countries have been promoting carbon capture, storage (CCS) projects in order to alleviate climate degradation and achieve net zero carbon emissions. To study the thermal effects of organic porous media on CO2 absorption and desorption, molecular dynamics coupled with Monte Carlo (MDMC) were used in this study. A part of the CO2 molecules will be trapped within kerogen matrix due to its complex porous structure. The affinity of kerogen to CO2 facilitates CO2′s adsorption within the kerogen porous media, resulting in a heterogeneous distribution of CO2. The kerogen forms high potential energy peaks and low potential energy wells in the matrix, which provide preferred adsorption sites for CO2 in the porous space. The low stress state of CO2 also indicates that it prefers adsorption in the matrix as CO2 performs a lower potential energy state in the kerogen matrix than in the bulk phase. This study examines different thermal effects of kerogen, and results indicate that increasing CO2 thermal motion facilitates its absorption, while a high temperature matrix promotes CO2 desorption. Adsorbed layer provides resistance for CO2′s diffusion behaviors. The free energy of CO2′s diffusion is analyzed in relation to its mechanism, revealing that irregular thermal motion causes uncertainty in the adsorption capacity.

Advancing thermal control in buildings with innovative cementitious mortar and recycled expanded glass/n-octadecane phase change material composites

This study delves into the role of phase change materials (PCMs) in bolstering energy efficiency, particularly in response to escalating global energy consumption in construction. The research focuses on integrating recycled expanded glass (REG) as a support material for shape-stabilized PCMs, specifically emphasizing n-octadecane (nOD) in cement mortars. With nOD exhibiting a melting point around 27 °C and a high latent heat thermal energy storage (TES) capacity of 241 J/g, various analyses, including DSC, FT-IR, SEM, TGA, and thermoregulation tests, assess the impact of different nOD/REG concentrations on TES properties. Alterations in physico-mechanical properties of mortar mixtures are noted with increasing REG/nOD content, impacting porosity and water absorption. The incorporation of REG/nOD PCMs decreases thermal conductivity, from 0.3620 W/mK (no PCM) to 0.1494 W/mK (full replacement). Thermo-regulation tests highlight PCM’s ability to counteract temperature fluctuations, surpassing results from other studies. Temperature difference outcomes (−10.60 °C daytime cooling, 4.00 °C nighttime heating) establish REG/nOD as promising for sustainable construction. The research evaluates PCM-infused concrete’s impact on building energy efficiency, noting significant heat demand reductions across climates and wall thicknesses. Carbon emissions decrease notably, especially with coal as the fuel source. Customized material thickness in PCM-integrated walls shows potential for substantial energy savings. These findings contribute valuable insights to the viability of REG/nOD composites in mitigating heating and cooling loads, advancing sustainable building solutions.

Sustaining Surface Lithiophilicity of Ultrathin Li-Alloy Coating Layers on Current Collector for Zero-Excess Li-Metal Batteries.

Zero-excess Li-metal batteries (ZE-LMBs) have emerged as the ultimate battery platform, offering an exceptionally high energy density. However, the absence of Li-hosting materials results in uncontrolled dendritic Li deposition on the Cu current collector, leading to chronic loss of Li inventory and severe electrolyte decomposition, limiting its full utilization upon cycling. This study presents the application of ultrathin (≈50nm) coatings comprising six metallic layers (Cu, Ag, Au, Pt, W, and Fe) on Cu substrates in order to provide insights into the design of Li-depositing current collectors for stable ZE-LMB operation. In contrast to non-alloy Cu, W, and Fe coatings, Ag, Au, and Pt coatings can enhance surface lithiophilicity, effectively suppressing Li dendrite growth, thereby improving Li reversibility. Considering the distinct Li-alloying behaviors, particularly solid-solution and/or intermetallic phase formation, Pt-coated Cu current collectors maintain surface lithiophilicity over repeated Li plating/stripping cycles by preserving the original coating layer, thereby attaining better cycling performance of ZE-LMBs. This highlights the importance of selecting suitable Li-alloy metals to sustain surface lithiophilicity throughout cycling to regulate dendrite-less Li plating and improve the electrochemical stability of ZE-LMBs.

Reduced Graphene Oxide Wrapped Polypyrrole on Carbon Cloth for High‐Performance Flexible Solid‐State Supercapacitors

AbstractThe nature of rigidity and low energy density of polypyrrole (PPy)‐based electrodes limits their wide application in flexible energy storage devices. In this study, reduced graphene oxide (rGO) wrapped polypyrrole (PPy)/oxidized carbon cloth (OCC) (rGO@PPy/OCC) is prepared by the polymerization of pyrrole using MnO2 as the oxidant on the surface of OCC followed by the adsorption and reduction of graphene oxide (GO). The prepared rGO@PPy/OCC electrode exhibits a high gravimetric specific capacitance of 547 F g−1 at a current density of 0.5 A g−1 and a high area specific capacitance of 1641 mF cm−2 at a current density of 1.5 mA cm−2. It nearly maintains the initial capacitance after 8000 cycles at a high scan rate of 200 mV s−1 and at a large current density of 10 A g−1. Moreover, the flexible rGO@PPy/OCC electrodes are used to construct flexible solid‐state supercapacitors (FSSC). The FSSC based on rGO@PPy/OCC exhibits a high energy density (33.89 Wh kg−1 and 101.81 µWh cm−2) and a capacitance retention of 95.10% after 1000 bending cycles, demonstrating the excellent cycling stability and flexibility. Therefore, it is potential for rGO@PPy/OCC as a flexible electrode to fabricate high‐performance FSSC.

Sustaining Surface Lithiophilicity of Ultrathin Li-Alloy Coating Layers on Current Collector for Zero-Excess Li-Metal Batteries.

Zero-excess Li-metal batteries (ZE-LMBs) have emerged as the ultimate battery platform, offering an exceptionally high energy density. However, the absence of Li-hosting materials results in uncontrolled dendritic Li deposition on the Cu current collector, leading to chronic loss of Li inventory and severe electrolyte decomposition, limiting its full utilization upon cycling. This study presents the application of ultrathin (≈50nm) coatings comprising six metallic layers (Cu, Ag, Au, Pt, W, and Fe) on Cu substrates in order to provide insights into the design of Li-depositing current collectors for stable ZE-LMB operation. In contrast to non-alloy Cu, W, and Fe coatings, Ag, Au, and Pt coatings can enhance surface lithiophilicity, effectively suppressing Li dendrite growth, thereby improving Li reversibility. Considering the distinct Li-alloying behaviors, particularly solid-solution and/or intermetallic phase formation, Pt-coated Cu current collectors maintain surface lithiophilicity over repeated Li plating/stripping cycles by preserving the original coating layer, thereby attaining better cycling performance of ZE-LMBs. This highlights the importance of selecting suitable Li-alloy metals to sustain surface lithiophilicity throughout cycling to regulate dendrite-less Li plating and improve the electrochemical stability of ZE-LMBs.

Lithiation Depth Regulation of Silicon Anodes toward Excellent Stability.

Silicon (Si) is an appealing choice of anode for next-generation lithium ion batteries with high energy density, but its dramatic volume expansion makes it a tremendous challenge to achieve acceptable stability. Herein, we demonstrate that no capacity decay is observed during the testing period when the lithiation depth of Si nanoparticles is regulated at 2000 mAh g-1 or below, the fracture of Si anode films is well mitigated under suitable regulation of lithiation depth, and the cycled Si remains particulate without turning flocculent as under full lithiation. In addition, the solid electrolyte interphase (SEI) with a LiF-dominated outer region produced under lithiation regulation could better passivate the Si anodes and prevent further electrolyte decomposition than the mosaic-type SEI formed under full lithiation. Regulating lithiation depth proved to be a feasible solution to the pressing volume issues, and optimization of capacity utilization should be considered as much as materials-level optimization.