Charge Diffusion Research Articles

Conductometric and Thermodynamic Studies of Selected Imidazolium Chloride Ionic Liquids in N,N-Dimethylformamide at Temperatures from 278.15 to 313.15 K.

This scientific article presents research on the electrical conductivity of imidazole-derived ionic liquids (1-methylimidazolium chloride, 1-ethyl-3-methylimidazolium chloride, 1-butyl-3-methylimidazolium chloride, 1-hexyl-3-methylimidazolium chloride and 1-methyl-3-octylimidazolium chloride) in the temperature range of 278.15-313.15 K in N,N-Dimethylformamide. The measurement methods employed relied mainly on conductometric measurements, enabling precise monitoring of the conductivity changes as a function of temperature. Experiments were conducted at various temperature values, which provided a comprehensive picture of the conducting properties of the investigated ionic liquids. The focus of the study was the analysis of the conductometric results, which were used to determine the conductivity function as a function of temperature. Based on the obtained data, a detailed analysis of association constants (KA) and thermodynamic parameters such as enthalpy (∆H0), entropy (∆S0), Gibbs free energy (∆G0), Eyring activation enthalpy for charge transport (ΔHλ‡) and diffusion processes (D0) was carried out. The conductometric method proved to be an extremely effective tool for accurately determining these parameters, significantly contributing to the understanding of the properties of imidazole-derived ionic liquids in the investigated temperature range. As a result, the obtained results not only provide new insights into the electrical conductivity of the studied ionic liquids but also broaden our knowledge of their thermodynamic behavior under different temperature conditions. These studies may have significant implications for the field of ionic liquid chemistry and may be applied in the design of modern materials with desired conducting properties.

MoS2 Hollow Multishelled Nanospheres Doped Fe Single Atoms Capable of Fast Phase Transformation for Fast‐charging Na‐ion Batteries

AbstractLow Na+ and electron diffusion kinetics severely restrain the rate capability of MoS2 as anode for sodium‐ion batteries (SIBs). Slow phase transitions between 2H and 1T, and from NaxMoS2 to Mo and Na2S as well as the volume change during cycling, induce a poor cycling stability. Herein, an original Fe single atom doped MoS2 hollow multishelled structure (HoMS) is designed for the first time to address the above challenges. The Fe single atom in MoS2 promotes the electron transfer, companying with shortened charge diffusion path from unique HoMS, thereby achieving excellent rate capability. The strong adsorption with Na+ and self‐catalysis of Fe single atom facilitates the reversible conversion between 2H and 1T, and from NaxMoS2 to Mo and Na2S. Moreover, the buffering effect of HoMS on volume change during cycling improves the cyclic stability. Consequently, the Fe single atom doped MoS2 quadruple‐shelled sphere exhibits a high specific capacity of 213.3 mAh g−1 at an ultrahigh current density of 30 A g−1, which is superior to previously‐reported results. Even at 5 A g−1, 259.4 mAh g−1 (83.68 %) was reserved after 500 cycles. Such elaborate catalytic site decorated HoMS is also promising to realize other “fast‐charging” high‐energy‐density rechargeable batteries.

Traversable wormholes via a double trace deformation involving U(1) conserved current operators

We study the effects of conservation laws on wormholes that are made traversable by a double trace deformation. After coupling the two asymptotic boundaries of a maximally extended (d+1)-dimensional black brane geometry with U(1) conserved current operators, we find that the quantum matter stress-energy tensor of the corresponding bulk gauge fields in the hydrodynamic limit violates the averaged null energy condition, rendering the wormhole traversable. Applying our results to axionic two-sided black hole solutions, we discuss how the wormhole opening depends on the charge diffusion constant, how this affects the amount of information that can be sent through the wormhole, and possible implications for many-body quantum teleportation protocols involving conserved current operators. Published by the American Physical Society 2024

MoS2 Hollow Multishelled Nanospheres Doped Fe Single Atoms Capable of Fast Phase Transformation for Fast-charging Na-ion Batteries.

Low Na+ and electron diffusion kinetics severely restrain the rate capability of MoS2 as anode for sodium-ion batteries (SIBs). Slow phase transitions between 2H and 1T, and from NaxMoS2 to Mo and Na2S as well as the volume change during cycling, induce a poor cycling stability. Herein, an original Fe single atom doped MoS2 hollow multishelled structure (HoMS) is designed for the first time to address the above challenges. The Fe single atom in MoS2 promotes the electron transfer, companying with shortened charge diffusion path from unique HoMS, thereby achieving excellent rate capability. The strong adsorption with Na+ and self-catalysis of Fe single atom facilitates the reversible conversion between 2H and 1T, and from NaxMoS2 to Mo and Na2S. Moreover, the buffering effect of HoMS on volume change during cycling improves the cyclic stability. Consequently, the Fe single atom doped MoS2 quadruple-shelled sphere exhibits a high specific capacity of 213.3 mAh g-1 at an ultrahigh current density of 30 A g-1, which is superior to previously-reported results. Even at 5 A g-1, 259.4 mAh g-1 (83.68 %) was reserved after 500 cycles. Such elaborate catalytic site decorated HoMS is also promising to realize other "fast-charging" high-energy-density rechargeable batteries.

Green zinc/galactomannan-based hydrogels push up the photovoltage of quasi solid aqueous dye sensitized solar cells

In the present work, we implement environmentally friendly water-based Quasi-Solid Electrolytes (QSE) for Dye Sensitized Solar Cells (DSSCs), displaying an unprecedent open circuit voltage (VOC) as high as 750 mV. The production of the hydrogel for QSE-DSSCs is achieved by exploiting the concept of fully green design and fabrication, through the selection of components such as the natural polysaccharide galactomannan (GM), biocompatible zinc salts, and the employment of eco-friendly synthetic procedures to produce the hybrid gelating agents. In the process, moderate temperature (<40 °C), only aqueous solutions are employed, and, at most, ethanol is used in some phases of the procedure. Depending on the type of the initial salt, either zinc hydroxysulfate lamellae or zinc oxide nanoparticles are created within the gel matrix, with a more extended nanoporous structure in the latter case. The nanostructures and the gels are investigated by multiple techniques, including X-ray diffraction (XRD), infrared spectroscopy (IR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). Upon ensuing addition of I-/I3- redox mediator and assembling of the device, state-of-the-art aqueous QSE-DSSCs are achieved. The latter couples a 2 % efficiency (limited by charge diffusion as proved by Electrochemical Impedance Spectroscopy) with a good Average Visible Transmittance (AVT), and Light Utilization Efficiency (LUE), a couple of coveted features in wave-selective or semi-transparent devices. Finally, Linear Response-Time Dependent DFT (LR-TDDFT) simulations are carried out on a model iodine/iodide layered zinc hydroxy sulphate structure towards a better understanding of the mechanism responsible for the high AVT.

Research on interference compensation methods for color image sensors based on iterative learning

PurposeFixed mode noise and random mode noise always exist in the image sensor, which affects the imaging quality of the image sensor. The charge diffusion and color mixing between pixels in the photoelectric conversion process belong to fixed mode noise. This study aims to improve the image sensor imaging quality by processing the fixed mode noise.Design/methodology/approachThrough an iterative training of an ergoable long- and short-term memory recurrent neural network model, the authors obtain a neural network model able to compensate for image noise crosstalk. To overcome the lack of differences in the same color pixels on each template of the image sensor under flat-field light, the data before and after compensation were used as a new data set to further train the neural network iteratively.FindingsThe comparison of the images compensated by the two sets of neural network models shows that the gray value distribution is more concentrated and uniform. The middle and high frequency components in the spatial spectrum are all increased, indicating that the compensated image edges change faster and are more detailed (Hinton and Salakhutdinov, 2006; LeCun et al., 1998; Mohanty et al., 2016; Zang et al., 2023).Originality/valueIn this paper, the authors use the iterative learning color image pixel crosstalk compensation method to effectively alleviate the incomplete color mixing problem caused by the insufficient filter rate and the electric crosstalk problem caused by the lateral diffusion of the optical charge caused by the adjacent pixel potential trap.

Ultrafast Charge Transfer Cascade in a Mixed-Dimensionality Nanoscale Trilayer.

Innovation in optoelectronic semiconductor devices is driven by a fundamental understanding of how to move charges and/or excitons (electron-hole pairs) in specified directions for doing useful work, e.g., for making fuels or electricity. The diverse and tunable electronic and optical properties of two-dimensional (2D) transition metal dichalcogenides (TMDCs) and one-dimensional (1D) semiconducting single-walled carbon nanotubes (s-SWCNTs) make them good quantum confined model systems for fundamental studies of charge and exciton transfer across heterointerfaces. Here we demonstrate a mixed-dimensionality 2D/1D/2D MoS2/SWCNT/WSe2 heterotrilayer that enables ultrafast photoinduced exciton dissociation, followed by charge diffusion and slow recombination. Importantly, the heterotrilayer serves to double charge carrier yield relative to a MoS2/SWCNT heterobilayer and also demonstrates the ability of the separated charges to overcome interlayer exciton binding energies to diffuse from one TMDC/SWCNT interface to the other 2D/1D interface, resulting in Coulombically unbound charges. Interestingly, the heterotrilayer also appears to enable efficient hole transfer from SWCNTs to WSe2, which is not observed in the identically prepared WSe2/SWCNT heterobilayer, suggesting that increasing the complexity of nanoscale trilayers may modify dynamic pathways. Our work suggests "mixed-dimensionality" TMDC/SWCNT based heterotrilayers as both interesting model systems for mechanistic studies of carrier dynamics at nanoscale heterointerfaces and for potential applications in advanced optoelectronic systems.

A NUMERICAL ANALYSIS ON THE SUBMICRON- AND MICRON-SIZED PARTICLE SEDIMENTATION IN A WIRE-TO-PLATE ELECTROSTATIC PRECIPITATOR

Electrostatic precipitators (ESPs) are frequently utilized in collecting fine organic and inorganic materials from continuous liquid with few moving parts and high efficiency using electrically charging the particles. In this study, cross-sectional 2D geometry of a wire-to-plate electrostatic precipitator the parametric data of which originally published elsewhere was numerically modeled and validated to investigate submicron-micron particle charging in terms of diffusion and field charging mechanisms and precipitation behavior of particles with detailed electric field properties. Electric field, gas flow, and particle trajectory equations are coupled and solved in a multiphysics solver. Particle tracking is realized with the Lagrangian approach. Results indicate variations in electric field strength and space charge density between corona electrodes, with space charge present in the entire precipitation channel. Between two different charging mechanisms, diffusion charging prevails for charge accumulated on submicron particles, whereas field charging becomes dominant for particles larger than 1μm diameter. However, for the ESP configuration considered in this study, particles reach a charge saturation in less than 0.7 seconds, regardless of their size. Although calculated precipitation efficiencies for micron-sized particles can reach to 100%, efficiencies for submicron particle range drop with increasing particle size, as diffusion charging rapidly loses its effectiveness, in 50-250nm range.

Gradient‐Tuned VO4 Vacancies in BiVO4 Photoanode for Boosting Bulk Hole Transport and Oxygen Evolution Reaction Performance

AbstractAlthough bismuth vanadate (BiVO4) photoanode has been widely used, the solar‐driven oxygen evolution reaction (OER) performance is constrained due to the substantial bulk recombination and poor mobility of charge carriers. Herein, a facile solvothermal post‐treatment approach that employs N,N‐dimethylformamide (DMF) is developed to induce a VO4 vacancy gradient from bulk to surface of BiVO4 film, which not only improves the charge diffusion but also establishes an advantageous upward band gradient to promote the bulk hole transport. Under Air Mass 1.5 Global (AM1.5G) simulated solar illumination, the optimized BiVO4 photoanode with a VO4 vacancy gradient (denoted as B(VO)1‐δ) exhibits excellent OER performance with a charge separation efficiency of 74.4% at 1.23 V versus reversible hydrogen electrode (RHE) and incident‐photon‐to‐current conversion efficiency of 30.7% at 445 nm, 1.2 and 1.4 times higher than that of the pristine BiVO4, respectively. After loading nickel‐iron hydroxyl oxide (NiFeOOH) as a cocatalyst, the photocurrent density of B(VO)1‐δ escalates to 5.92 mA cm−2 in a hole scavenger (Na2SO3) solution and 5.07 mA cm−2 in a potassium borate buffer solution at 1.23 V versus RHE, far superior to the pristine BiVO4. This work highlights that the gradient‐tuned VO4 vacancies can effectively modulate the bulk band structure and charge transfer in BiVO4 photoanode, providing a new strategy for boosting solar water splitting performance.

Activation of MnO6 Units via an Interfacial Electric Field: Electron Injection into Mn t2g for Rapid and Stable Sodium Ion Storage in CeO2/MnOx.

Manganese-based oxides (MnOx) suffer from sluggish charge diffusion kinetics and poor cycling stability in sodium ion storage. Herein, an interfacial electric field (IEF) in CeO2/MnOx is constructed to obtain high electronic/ionic conductivity and structural stability of MnOx. The as-designed CeO2/MnOx exhibits a remarkable capacity of 397 F g-1 and favorable cyclic stability with 92.13% capacity retention after 10,000 cycles. Soft X-ray absorption spectroscopy and partial density of states results reveal that the electrons are substantially injected into the Mn t2g orbitals driven by the formed IEF. Correspondingly, the MnO6 units in MnOx are effectively activated, endowing the CeO2/MnOx with fast charge transfer kinetics and high sodium ion storage capacity. Moreover, In situRaman verifies a remarkably increased structural stability of CeO2/MnOx, which is attributed to the enhanced Mn─O bond strength and efficiently stabilized MnO6 units. Mechanism studies show that the downshift of Mn 3d-band center dramatically increases the Mn 3d-O 2p orbitals overlap, thus inhibiting the Jahn-Teller (J-T) distortion of MnOx during sodium ion insertion/extraction. This work develops an advanced strategy to achieve both fast and sustainable sodium ion storage in metal oxides-based energy materials.

Mitigation of charge heterogeneity by uniform in situ coating enables stable cycling of LiCoO2 at 4.6V

LiCoO2 is a predominant cathode for lithium-ion batteries of portable electronics owing to its merit of high volumetric energy density. Nevertheless, it experiences rapid capacity deterioration under high voltages, concomitant with structural degradation and numerous intragranular cracks. Coating has been recognized as an efficacious strategy to ameliorate the decline in cycling performance of LiCoO2 at high voltages. Hence, a systematic elucidation of the precise mechanisms underlying the mitigation of structural degradation via coating layers assumes paramount importance in the context of advancing the next generation of high-voltage LiCoO2. In this work, the intricate interrelation among lithium-ion diffusion coefficients, charge heterogeneity, and crack distribution is explicated through techniques inclusive of galvanostatic intermittent titration technique (GITT), finite element analysis (FEA), and X-ray computed tomography (XCT). A robustly stable lithium-ion-conducting coating material serves the function of curtailing the occurrence of surface passivation layers, achieved by diminishing side reactions between the LiCoO2 and the electrolyte; while a uniform coating ensures a homogeneous lithium-ion flux, thereby mitigating charge heterogeneity and the resultant mechanical strain as well as intragranular cracks. Both are important elements that collectively allow the coating to effectively protect the surface from structural degradation, thus achieving superior performances upon high-voltage charging.

Unlocking Charge Transfer Limitation in NASICON Structured Na3V2(PO4)3 Cathode via Trace Carbon Incorporation

AbstractNASICON‐type cathode with remarkable ionic conductivity is perspective candidate for fast‐charging sodium‐ion battery. However, severely restricted by low electrical conductivity and poor interfacial kinetics, it usually delivers poor charge transfer kinetics. Different from traditional carbon compositing with high carbon contents, herein, a trace carbon incorporation tactic is proposed based on a typical NASICON‐structured Na3V2(PO4)3. First, particle‐growth process of Na3V2(PO4)3 is regulated via incorporating carbon dot, significantly reducing its particle size to shorten charge diffusion path. Second, electrical conductivity of Na3V2(PO4)3 is improved without sacrificing its high electrochemical activity due to the incorporated trace carbon content (0.76 wt.%). Third, Na3V2(PO4)3‐electrolyte interface structure is optimized by abundant functional groups from the incorporated carbon dot, enabling a thin and stable NaF‐rich CEI layer to boost interface kinetics. As a result, carbon dot endows Na3V2(PO4)3 with ultrastable cyclability up to 20 k cycles (capacity retention of 98.4%) and excellent rate capability (up to 200 C) in half cell, as well as high energy density (368.7 Wh kg−1) and fast charging property (≈110.2 s per charging with 250.8 Wh kg−1 input) in full cell. This study carves a new path for developing fast‐charging cathode, as is increasingly desired for present energy storage applications.

High mass-loading CoO@NiCo-LDH//FeNiS flexible supercapacitor with high energy density and fast kinetics

The rapidly growing market of portable and wearable smart electronics has created strong interest in flexible electrode materials with high specific capacitance and fast charging/discharging properties. However, high mass-specific capacitance active materials are often limited by the low areal mass-loading required. High areal capacity electrodes can make more efficient use of the limited internal space of these miniature devices by minimizing the volume and weight taken by current collectors and separators. Herein, a method is proposed to prepare a nickel–cobalt layered double hydroxide binder-free cathode on flexible carbon cloth with a mass loading of 20 mg cm−2. This core–shell hybrid structure prepared using a MOF self-sacrificing template, achieves a high energy density using thick electrodes while improving their slow kinetics by enhancing both the ion diffusion process and charge transfer dynamics. The areal capacitance reaches a staggering 4.42 mAh cm−2 (31.79 F cm−2) at a current density of 8 mA cm−2. Furthermore, a one-step hydrothermal method to prepare the FeNi-S anode (1.67 mAh cm−2, 2 mA cm−2) is proposed. Upon assembling with the gel electrolyte, this flexible device possesses an impressive energy density of 3.29 mW h cm−2 (3 mW cm−2). It can readily supply energy to watches, wireless e-paper, LEDs, and can be anticipated to be widely used in next-generation high-performance portable and wearable devices.

Analytical solutions for viscoelectric effects in electrokinetic nanochannels.

Understanding electrokinetic transport in nanochannels and nanopores is essential for emerging biological and electrochemical applications. The viscoelectric effect is an important mechanism implicated in the increase of local viscosity due to the polarization of a solvent under a strong electric field. However, most analyses of the viscoelectric effect have been limited to numerical analyses. In this work, we present a set of analytical solutions applicable to the physical description of viscoelectric effects in nanochannel electrokinetic systems. To achieve such closed-form solutions, we employ the Debye-Hückel approximation of small diffuse charge layer potentials compared to the thermal potential. We analyze critical parameters, including electroosmotic flow profiles, electroosmotic mobility, flow rate, and channel conductance. We compare and benchmark our analytical solutions with published predictions from numerical models. Importantly, we leverage these analytical solutions to identify essential thermophysical and nondimensional parameters that govern the behavior of these systems. We identify scaling parameters and relations among surface charge density, ionic strength, and nanochannel height.

Recent Advancements in Enhancing Interfacial Charge Transport for Perovskite Solar Cells

Finding the most suitable pathways to improve the interfacial charge transportation in lead halide perovskite solar cells is a highly desirable research area to enhance device performance and enable commercialization. The complexities of interfacial charge dynamics, encompassing separation, diffusion, and collection processes, pivot on the thoughtful selection of interlayers and their inherent properties. Challenges arise from nonideal interfaces characterized by mismatched energy levels and defects that hinder efficient charge transport. To address these concerns, implementing tailored interfacial engineering strategies, including interlayer modification, band alignments, and passivation techniques, can help mitigate unwanted nonradiative recombination. This review aims to elucidate the impact of trap states on suppressing charge transport in the device, along with subsequent passivation techniques designed to enhance interfacial charge transport. Following that, a comprehensive overview is presented, highlighting recent advancements in interface engineering techniques that improve interfacial properties between the electron transport layer/perovskite and perovskite/hole transport layer. Significantly, the impact of using buffer and dipole layers as interlayers on overall device performance and stability is investigated.

Hierarchical and Nanocrystallite-Assembled Ultraporous NiO/MnCo2O4 for All Solid-State Hybrid Supercapacitors with Robust Energy Efficiency and Extended Operational Durability.

To address the growing demand of highly Ragone efficient electrochemical energy storage devices, we have innovated a synthetic design strategy and employed a tartrate-mediated kinetic precipitation process to fabricate an ultraporous ribbon-like hierarchical microstructure of Ni-, Mn-, and Co-based ternary oxide, i.e., NiO/MnCo2O4, and employed it as a battery-type positive electrode material to assemble an ASSHSC (all-solid-state hybrid supercapacitor) device with nitrogen-doped reduced graphene oxide (N-rGO) as the positive electrode material. NiO/MnCo2O4 exhibits distinct crystallographic phase, near-perfect elemental stoichiometry, evident bulk porosity, and rich nanocrystallite assembly in the randomly arranged microstructure of near-uniform size and shape. Thorough electrochemical studies corroborate that the battery-type NiO/MnCo2O4 exhibits remarkable electrochemical reversibility during charge transfer, high efficiency in supercapacitive charge storage, low charge transfer, series and diffusion resistance. The NiO/MnCo2O4||N-rGO ASSHSC device assembled with the PVA-KOH film as the separator electrolyte offers rich charge storage physiognomies, which accentuates excellent electromicrostructural compatibility between the electrode materials in the device. The NiO/MnCo2O4||N-rGO ASSHSC device shows low charge transfer and diffusion resistance, and it also delivers high mass and areal specific capacitance/capacity, energy and power density, Ragone efficiency (∼131 Wh kg-1 at ∼2134 W kg-1 and ∼31 Wh kg-1 at ∼5005 W kg-1), and extended operational durability (98.2% specific capacitance retention after 12,000 successive GCD cycles) under high-rate working conditions. The present optimized approach to design highly efficient multiple transition-metal-based oxides as battery-type electrode materials and fabricate rich Ragone-efficient ASSHSC devices can be widely adopted in the future development of high-performance hybrid supercapacitors, which may be largely integrated in various pioneering technologies.

Hollow Carbon and MXene Dual-Reinforced MoS2 with Enlarged Interlayers for High-Rate and High-Capacity Sodium Storage Systems.

Sodium-ion batteries (SIBs) and sodium-ion capacitors (SICs) are promising candidates for cost-effective and large-scale energy storage devices. However, sluggish kinetics and low capacity of traditional anode materials inhibit their practical applications. Herein, a novel design featuring a layer-expanded MoS2 is presented that dual-reinforced by hollow N, P-codoped carbon as the inner supporter and surface groups abundant MXene as the outer supporter, resulting in a cross-linked robust composite (NPC@MoS2/MXene). The hollow N, P-codoped carbon effectively prevents agglomeration of MoS2 layers and facilitates shorter distances between the electrolyte and electrode. The conductive MXene outer surface envelops the NPC@MoS2 units inside, creating interconnected channels that enable efficient charge transfer and diffusion, ensuring rapid kinetics and enhanced electrode utilization. It exhibits a high reversible capacity of 453 mAh g-1, remarkable cycling stability, and exceptional rate capability with 54% capacity retention when the current density increases from 100 to 5000mA g-1 toward SIBs. The kinetic mechanism studies reveal that the NPC@MoS2/MXene demonstrates a pseudocapacitance dominated hybrid sodiation/desodiation process. Coupled with active carbon (AC), the NPC@MoS2/MXene//AC SICs achieve both high energy density of 136Wh kg-1 at 254W kg-1 and high-power density of 5940W kg-1 at 27Wh g-1, maintaining excellent stability.

Engineered oxidation states in NiCo2O4@CeO2 nanourchin architectures with abundant oxygen vacancies for enhanced oxygen evolution reaction performance

Sluggish oxygen evolution reaction (OER) as the half reaction of water electrolysis hindered the production of clean hydrogen, necessitates a cost-effective electrocatalyst. Spinel nickel cobaltite (NiCo2O4), characterized by its lower cost, flexibility in oxidation states of cations, and stable spinel structure, holds promise as an OER electrocatalyst. However, there is still room for improvement in terms of its intrinsic electrochemical activity, conductivity, and active surface area. Inspired by the flexible valence states of Ni and Co, in this study, CeO2 was introduced into NiCo2O4 for further electronic structure adjustment. The result was the synthesis of an urchin-like NiCo2O4@CeO2 (NCOC), and the elucidation of its formation mechanisms, expressed conclusively through reaction formulas. NCOC, characterized by an open architecture and a rough surface, ensures rapid mass transportation and charge diffusion. Within NCOC, numerous oxophilic Ce3+ sites with oxygen vacancies construct electron transport pathways, accelerating charge-transfer. This simultaneously induces an increase in the oxidation states and proportions of Ni3+ and Co3+ in NCOC, reinforcing the covalence of Ni–O and Co–O bonds, expediting the ad/desorption of intermediates during OER. The electronic structure variations of NCOC were further verified through density functional theory (DFT) analyses, revealing alterations in adsorption configurations of intermediates and a decrease in adsorption free energies for intermediates on NCOC during OER. In practical terms, NCOC demonstrated a low overpotential of 228 mV at a current density of 10 mA cm−2 under 1 M KOH, maintaining long-term electrochemical stability for 100 h. Overall, this study provides a universal approach for designing highly cost-efficient electrocatalysts for OER.

Solid Particle Number (SPN) Portable Emission Measurement Systems (PEMS) for Heavy-Duty Applications

A heavy-duty engine is homologated in a test cell. However, starting with Euro VI regulation, the in-service conformity is controlled with the engine installed in the vehicle using portable emission measurement systems (PEMS). In Europe, the application of solid particle number (SPN) PEMS started in 2021 for compression ignition (diesel) vehicles and in 2023 for positive ignition vehicles, thus including those operating with compressed natural gas (CNG). Even though today only particles with sizes &gt; 23 nm are regulated, the Euro 7 proposal includes particles &gt; 10 nm. There are not many studies on the accuracy of the SPN PEMS, especially for heavy-duty applications. In this study, PEMS measuring &gt; 23 and &gt;10 nm from two instrument manufacturers were compared with laboratory-grade instruments. The particle detector of one PEMS was a condensation particle counter (CPC), and of the other a the diffusion charger (DC). The results showed the robustness and good accuracy (40% or 1 × 1011 #/kWh) of the PEMS for ambient temperatures from −7 °C to 35 °C, active regeneration events, different fuels (Diesel B7, HVO, and CNG), different test cycles, cold start or hot engine operations, and high exhaust gas humidity content. Nevertheless, for the DC-based PEMS, sensitivity to pre-charged urea particles was identified, and for the CPC-based PEMS, sensitivity to pressure changes with one vehicle was nnoticed. Nevertheless, the results of this study confirm that the PEMS are accurate enough to measure even the stricter Euro 7 limits.

Proton-Conductive COF Evenly Embedded Cellulose Aerogels toward Water Harvesting and Spontaneous Sustained Power Generation from Ambient Moisture and Human Respiration.

Herein, we develop a new intelligent moisture-sensitive hybrid aerogel by evenly embedding a proton-conductive covalent organic framework (COF-2SO3H) into a carboxylated cellulose nanofiber network (CNF-C) for water harvesting and spontaneous sustained electricity production from ambient humidity and human respiration. Our strategy first exploits the "suspending agent" role of CNF-C to stably disperse COF materials in water for forming uniform hierarchical hybrid structures. By utilizing the synergy of COF-2SO3H and CNF-C together with their inherent structure merits and surface group effects, the hybrid aerogel displays increased water uptake and ion conductivity. Upon asymmetric moisturization, it can create a self-maintained moisture gradient to engender a concentration difference for mobile Na+ and H+, resulting in efficient charge separation and diffusion. Thus, the hybrid aerogel-based coin-type generator achieves a continuous output voltage of ∼0.55 V for at least 5 h in ambient environments in contrast to that using pure CNF-C and carbon-based generators with transient voltage response. Intriguingly, the wearable generator with an aerogel in a mask is more sensitive to human respiration and achieves repeatable and reliable self-charge for persistent electricity along with an increased output voltage of up to 1.0 V and much faster self-charge (only 3 min), both of which surpass most reported moisture-enabled generators.