Electric Gradient Research Articles

Electrical Double Layer Spillover Drives Coupled Electron- and Phase-Transfer Reactions at Electrode/Toluene/Water Three-Phase Interfaces.

A mechanism for the concerted pathway of coupled electron- and phase-transfer reactions (CEPhT) is proposed. CEPhT at three-phase interfaces formed by a solid electrode, an insulating organic solvent, and an aqueous electrolyte is driven by electric double layer (EDL) spillover, with significant electrostatic potential gradients extending a few nanometers into the insulating phase. This EDL spillover phenomenon is studied using scanning electrochemical cell microscopy to interrogate the oxidation of ferrocene in toluene to ferrocenium in water, (Fc)tol → (Fc+)aq + e-. Finite element method simulations of the electrostatic potential distribution and species concentration profiles enable the calculation of complete i-E curves that incorporate mass transport, electron transfer, phase transfer, and the EDL structure. Simulated and experimental i-E traces show good agreement in the current magnitude and the effect of the supporting electrolyte, identifying an unexpected dependence of overall reaction kinetics on the concentration of the supporting electrolyte in the aqueous phase due to EDL spillover. An interfacial toluene/water mixing region generates a unique electrochemical microenvironment where concerted electron transfer and solvent shell replacement facilitate CEPhT. Kinetic expressions for concerted and sequential CEPhT mechanisms highlight the role of this interfacial environment in controlling the rate of CEPhT. These combined experimental and simulated results are the first to support a concerted mechanism for CEPhT where (Fc)tol is transported to the interfacial mixing region at the three-phase interface, where it undergoes oxidation and phase transfer. EDL spillover can be leveraged for engineering sample geometries and electrostatic microenvironments to drive electrochemical reactivity in classically forbidden regions, e.g., insulating solvents and gases.

Initiation of prefrontal convection within a Northeast China cold vortex: The roles of elevated front and dry air intrusion

AbstractConvective initiation ahead of a surface cold front within the Northeast China cold vortex of June 1, 2021, is investigated using observations and a convection‐permitting simulation. The initiation of the convection is elevated without identifiable surface mesoscale forcing. Air feeding the initial convective cells originates from at least 1 km above the ground where parcel‐based convective available potential energy is sufficiently large. An elevated front with large equivalent potential temperature gradient and flow convergence across is primarily responsible for the initiation of elevated convection and later organization into a deep convective line. The elevated front is similar to the upper cold front within extratropic cyclones studied elsewhere, but its altitude is lower in this case. Backward‐trajectory analysis of air parcels on the cold side of the elevated front shows that dry air intrusion reinforces the elevated front by increasing the equivalent potential temperature gradient and moment convergence across the front. The convergence forcing combined with access to convective unstable air at the leading edge of the westerly flows east of the elevated front causes the initiation of convection. The development and spreading of a surface cold pool help push the convective line eastward away from the surface cold front located to the west. Orographic gravity waves provide additional forcing so that convection cells are initiated first at the upward branches of the gravity waves, but the overall organization of initial cells into a solid convective line is controlled mainly by mesoscale structures associated with the elevated front.

Osmolytes and CsAQP expression jointly influence water physiology in the peel and pulp of orange (Citrus sinensis (L.) Osbeck) fruit during postharvest water loss

Water loss is a serious issue affecting the quality of postharvest horticultural products. Aquaporins (AQPs) regulate the transport of water across biological membranes, along the gradient of water potential, and may play a role in water loss. In this study, matured orange fruits (Citrus sinensis) stored at ambinent temperature (RH 85-95%) for 105 d showed that the weight loss persistently increased, and its rate peaked at 45–60 d and 90–105 d. Both water content and potential were higher in the pulp than in the peel. Water content rose before 60 d, and peel water potential fell with an increased gradient after 60 d. Comparing with peel, osmolytes such as soluble sugar, sucrose, glucose, fructose, and organic acids showed higher accumulation, and their levels were the lowest around 60 d. In contrast, soluble protein and inorganic minerals showed low levels of accumulation in the pulp. In total, 31 CsAQP genes were expressed in the fruit, and most of them were down-regulated in the peel but up-regulated in the pulp during storage. These genes were subsequently classified into four clusters based on their expression patterns. Genes in Cluster I — including CsNIP1;1/2;1/2;2/2;3/3;1/4;1/6;1, CsTIP1;3/2;2/2;3/5;1/6;1, CsXIP1;1/1;2, CsSIP1;2, and CsPIP1;2 — were persistently up-regulated in the pulp for the 105 d of storage, especially at day 60, when some genes showed 103-fold higher expression. Pearson’s correlation and principal component analysis further revealed a significant positive correlation among weight loss rate, water content, and water potential gradient (R2 = 0.85). Indexes positively correlated with osmolyte content and Cluster I gene expression in pulp samples suggest that increased CsAQP gene expression in pulp is linked to faster water loss in oranges, particularly at 60 days postharvest.

Computational Fluid Dynamics Modelling of Hydrogen Production via Water Splitting in Oxygen Membrane Reactors.

The utilization of oxygen transport membranes enables the production of high-purity hydrogen by the thermal decomposition of water below 1000 °C. This process is based on a chemical potential gradient across the membrane, which is usually achieved by introducing a reducing gas. Computational fluid dynamics (CFD) can be used to model reactors based on this concept. In this study, a modelling approach for water splitting is presented in which oxygen transport through the membrane acts as the rate-determining process for the overall reaction. This transport step is implemented in the CFD simulation. Both gas compartments are modelled in the simulations. Hydrogen and methane are used as reducing gases. The model is validated using experimental data from the literature and compared with a simplified perfect mixing modelling approach. Although the main focus of this work is to propose an approach to implement the water splitting in CFD simulations, a simulation study was conducted to exemplify how CFD modelling can be utilized in design optimization. Simplified 2-dimensional and rotational symmetric reactor geometries were compared. This study shows that a parallel overflow of the membrane in an elongated reactor is advantageous, as this reduces the back diffusion of the reaction products, which increases the mean driving force for oxygen transport through the membrane.

Constrained Hamiltonian dynamics for electrons in magnetic field and additional forces besides the Lorentz force acting on electrons

Abstract We consider the forces acting on electrons in magnetic field including the constraints and a condition arising from quantum mechanics. The force is calculated as the electron mass, m e , multiplied by the total time-derivative of the velocity field evaluated using the quantum mechanical many-electron wave function. The velocity field includes a term of the Berry connection from the many-body wave function; thereby, quantum mechanical effects are included. It is shown that additional important forces besides the Lorentz force exist; they include the gradient of the electron velocity field kinetic energy, the gradient of the chemical potential, and the ‘force’ for producing topologically protected loop currents. These additional forces are shown to be important in superconductivity, electric current in metallic wires, and charging of capacitors.

Impact of Dual Functionalities of Mo‐Doped BiFeO3 Decorated with Bi4MoO9 Heteroatoms for Piezo‐Photocatalytic Activity

AbstractPiezocatalysts have shown great promise for effcient hydrogen generation. However, their application is limited by the rapid charge recombination and sluggish charge transfer rate of piezo‐induced charge carriers. This work aims to address the preceding limitations by controlled synthesis of a representative piezocatalyst, BiFeO3 doped with Mo atoms and decorated with Bi4MoO9 (BMO) heteroatoms using sol‐gel method. The substitutional doping of Mo on BFO (BFMO) was shown to induce a shallow energy level near the conduction band that acted as a trapping state, to suppress recombination of charge carriers, enhance charge mobility for transport to the surface, modulate band alignment, and lower the energy barrier for surface reaction. The formation of BFMO/BMO heterostructures induced electrical band bending, leading to the electric potential gradient, hence promoting charge carrier separation and transfer. The BFMO/BMO with 0.5 mol % Mo (Mo‐5) demonstrated four times faster piezocatalytic Rhodamine B (RhB) dye degradation rate (k of 0.032 min−1) compared to pristine BFO (0.009 min−1). Further, the Mo‐5 exhibited a 45% higher piezocatalytic H2 production rate (14.4 µmol/g/h) compared to pristine BFO (9.8 µmol/g/h) while being cocatalyst‐free. Coupling piezocatalysis with photocatalysis was found to reduceperformance relative to the individual processes, which is attributed to Auger recombination which impedes any potential synergistic effect.

Electrokinetic remediation of cadmium-contaminated soil using polarity reversal method: Optimization analysis and mechanism exploration

Electrokinetic remediation (EKR) has been applied for in-situ removal of Cd from contaminated soil, and the EKR enhanced with polarity reversal has achieved a higher Cd removal efficiency. However, the migration and accumulation mechanisms of Cd in the EKR process have not been investigated. In this paper, the cross-impacts of the voltage gradient, citric acid concentration in the electrolyte, and polarity reversal frequency on the removal efficiency by EKR of Cd and the optimization conditions were investigated. The migration and accumulation mechanisms of Cd were explored by analyzing the changes in electrokinetic process parameters, experimental phenomena, and X-ray diffraction (XRD) analysis. The results showed that the maximum removal efficiency of Cd reached 82.26%. The optimal conditions were determined by fitting the RSM model using the BBD design. In the EKR experiment with polarity reversal, Cd accumulated mainly in the middle part of the soil, attributed to the formation of chemical precipitation focusing area caused by soil pH transition, ion-induced potential gradient well trapping effect (IIPGWTE), or soil compaction induced by water loss. In conclusion, the various parameters have cross-impacts on the EKR of Cd-contaminated soil, and efficient in-situ removal of Cd from the contaminated soil can be achieved by adjusting the parameter conditions.

Intertwined Flexoelectricity and Stacking Ferroelectricity in Marginally Twisted hBN Moiré Superlattice.

Moiré superlattices in twisted van der Waals homo/heterostructures present a fascinating interplay between electronic and atomic structures, with potential applications in electronic and optoelectronic devices. Flexoelectricity, an electromechanical coupling between electric polarization and strain gradient, is intrinsic to these superlattices because of the lattice misfit strain at the atomic scale. However, due to its weak magnitude, the effect of flexoelectricity on moiré ferroelectricity has remained underexplored. Here, the role of flexoelectricity in shaping and modulating the moiré ferroelectric patterns in twisted hBN homojunction is unveiled. Enhanced flexoelectric effects induce unique stacking ferroelectric domains with hollow triangular structures. Interlayer bubbles influence domain shape and periodicity through local electric field modulation, and tip-stress enables the reversible manipulation of domain area and polarization direction. These findings highlight the impact of flexoelectric effects on moiré ferroelectricity, offering a new tuning knob for its manipulation.

Ionic selectivity of nanopores: Comparison among cases under the hydrostatic pressure, electric field, and concentration gradient

The ionic selectivity of nanopores is crucial for the energy conversion based on nanoporous membranes. It can be significantly affected by various parameters of nanopores and the applied fields driving ions through porous membranes. Here, with finite element simulations, the selective transport of ions through nanopores is systematically investigated under three common fields, i.e. the electric field (V), hydrostatic pressure (p), and concentration gradient (c). For negatively charged nanopores, through the quantitative comparison of the cation selectivity (t+) under the three fields, the cation selectivity of nanopores follows the order of t+V > t+c > t+p. This is due to the transport characteristics of cations and anions through the nanopores. Because of the strong transport of counterions in electric double layers under electric fields and concentration gradients, the nanopore exhibits a relatively higher selectivity to counterions. We also explored the modulation of t+ on the properties of nanopores and solutions. Under all three fields, t+ is directly proportional to the pore length and surface charge density, and inversely correlated to the pore diameter and salt concentration. Under both the electric field and hydrostatic pressure, t+ has almost no dependence on the applied field strength or ion species, which can affect t+ in the case of the concentration gradient. Our results provide detailed insights into the comparison and regulation of ionic selectivity of nanopores under three fields which can be useful for the design of high-performance devices for energy conversion based on nanoporous membranes.

Motivating Mechanisms of the South Asian Jet Wave Train by Disturbances over the North Atlantic in Winter

Abstract This study investigated the motivation of the South Asian jet wave train (SAJW) and its underlying mechanism, by distinguishing different evolutions of disturbance sources over the North Atlantic. The disturbance sources propagate along the SAJW toward the western North Pacific in the propagating cases, while they are constrained over the North Atlantic and Europe in the interrupted cases. The possible motivating mechanisms are disclosed in the perspectives of energy dispersion and background potential vorticity gradient (PVG) affecting energy attraction. In the propagating cases, wave energy propagates eastward over the North Atlantic and converges into the Mediterranean Sea and Middle East, leading to the amplification and development of the wave train. The enhancement of PVG over south Europe–Mediterranean Sea is a key factor attracting such eastward propagation, which is associated with the positive PV anomaly over north Europe driven by the diabatic heating of precipitation. In the interrupted cases, energy dispersion is more divergent over the North Atlantic because of the weaker PVG, resulting in the failure of the SAJW excitement. The impacts of the SAJW on the temperature and precipitation along its path are evident, with the modulated snow depth agreeing more with temperature rather than precipitation except over the Tibetan Plateau. Hence, understanding the motivating mechanism of the SAJW is essential for improving weather forecasts over subtropical Eurasia by using the disturbances over the North Atlantic.

Origin of ventricular fibrillation triggers in a model of localized repolarization heterogeneity

BackgroundHeterogeneities in ventricular repolarization contribute significantly to the genesis of ventricular fibrillation (VF). Although clinical arrhythmias are spontaneously triggered by premature ventricular complexes, these triggers are difficult to document and little is known about their site of origin. ObjectiveTo characterize spontaneous VF initiation in an experimental model of repolarization heterogeneity and to identify the origin of triggers in relation to the spatial dispersion of repolarization. MethodsSpatially limited repolarization heterogeneity was created in isolated perfused porcine right ventricles (N =16) by local administration of pinacidil (20 μM) into a terminal branch of the right coronary artery. High-resolution optical mapping and pseudo-ECG were performed in control conditions and after pinacidil perfusion. ResultsNo arrhythmia occurred at baseline, but 74 VF episodes were observed in 13 hearts (82%) after pinacidil perfusion and were most often initiated by a ventricular trigger with short coupling interval (297±66ms). Sixteen VF initiations were optically mapped in four hearts. Mapping showed triggers originating in all cases from the border zone between altered and normal repolarization areas where local action potential duration and repolarization time gradients were steep (15.9 and 15.8 ms/mm versus 1.5 and 3.0 ms/mm in non-trigger sites). Optical action potential traces were compatible with a phase-two reexcitation mechanism. The subsequent VF cycles were driven by activities located in the same region. ConclusionsThis model of localized repolarization heterogeneity is able to produce spontaneous VF initiation. Our study demonstrates that VF triggers originate consistently from the border zone of repolarization dispersion.

Purification, characterization, and antimicrobial mechanism of a novel broad-spectrum bacteriocin produced by Lactiplantibacillus plantarum SCA12 from Traditional Chinese Fermented Mustard greens

In this study, Lactiplantibacillus plantarum SCA12, a producer of bacteriocins, derived from traditional Chinese fermented mustard greens was isolated. A novel L. plantarum SCA12-derived bacteriocin, LPsca12, was purified through a multi-step protocol involving macroporous adsorption resin, cation exchange, Sephadex G-25 column chromatography, and reverse-phase high-performance liquid chromatography (RP-HPLC). The molecular mass of LPsca12 was determined to be 1197.0 Da through matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis. The amino acid sequence of LPsca12 was characterized as GLFPSLVRGPR via liquid chromatography-tandem mass spectrometry (LC-MS/MS). Antimicrobial assessment was then carried out, identifying LPsca12 as a broad-spectrum bacteriocin active against both Gram-negative and Gram-positive bacteria, particularly Salmonella paratyphi A. It demonstrates excellent thermal stability (121 °C, 15 min) and maintains its antibacterial activity under acidic conditions (pH 2.0–6.5). Additionally, LPsca12 is sensitive to digestion by pepsin and trypsin. The antimicrobial action of LPsca12 involves compromising the cell membrane integrity, forming pores, and promoting leakage of intracellular contents, which dissipates both the membrane potential (ΔΨ) and cytoplasmic transmembrane pH gradient (ΔpH) of the target cells. These findings suggest that LPsca12 holds promise as a natural biopreservative in food processing.

Water vapor corrosion behavior of SiC-Al40Y ceramics fabricated by reactive melt infiltration and thermal diffusion

The corrosion resistance of Y-Al diffused SiC ceramics (SiC-Al40Y) at 1100-1300 °C was investigated. The results show that the weight gain curves comply with the parabolic fitting formula, then the oxidation rate constant and the activation energy were calculated to be 1.653×10-5 (1100 °C), 3.704×10-5 (1200 °C), 9.306×10-5 (1300 °C) mg2/cm4s and 154.7 kJ/mol. Compared with reported SiC (41-147 kJ/mol), the higher activation energy indicates the better corrosion-resistant performance. And it is found that the Y-Al diffusion layers can be transformed to corrosion-resistant YAlSixOy layers under corrosive atmosphere. Eventually, based on experimental results, the corrosion-resistant mechanism is analyzed: chemical potential gradient caused by preferential oxidation of Y-Al prompts the immigration of Y-Al from matrix to surface, gradually forming a continuous Y/Al-silicate layer on the surface and thus can hinder the further corrosion of H2O, O2.

Mathematical Model of Double-Pulse Electrolysis of Alkalines

A mathematical model of a simple two-chamber electrolyzer was formulated and substantiated for the study of possible processes occurring during electrolysis. In the calculations, the following factors were taken into the account: electrochemical reactions, electromigration of ions in the potential gradient field, diffusion through the membrane that separates the cathode and anode chambers, the change in the volume of the solution due to the water molecules compaction in the hydration shells of ions, and the change in the alkali concentration. The electrolysis mode consists of two consecutive current pulses: the first-cathodic and the next – anodic. Theoretical calculations of the system state in the two-pulse mode are the most accurate since the chemical composition of the electrolyte does not change at the moment of switching the current. However, the directions of electrode reactions, electromigration, and electroosmosis change. In the electrolysis mode with more pulses, it would be impossible to calculate the state parameters. A mathematical model was created for a comparative analysis of the influence of different electrolysis conditions on the speed ratio of various processes.

Photoelectron-promoted metabolism of sulphate-reducing microorganisms in substrate-depleted environments.

Sulphate-reducing microorganisms, or SRMs, are crucial to organic decomposition, the sulphur cycle, and the formation of pyrite. Despite their low energy-yielding metabolism and intense competition with other microorganisms, their ability to thrive in natural habitats often lacking sufficient substrates remains an enigma. This study delves into how Desulfovibrio desulfuricans G20, a representative SRM, utilizes photoelectrons from extracellular sphalerite (ZnS), a semiconducting mineral that often coexists with SRMs, for its metabolism and energy production. Batch experiments with sphalerite reveal that the initial rate and extent of sulphate reduction by G20 increased by 3.6 and 3.2 times respectively under light conditions compared to darkness, when lactate was not added. Analyses of microbial photoelectrochemical, transcriptomic, and metabolomic data suggest that in the absence of lactate, G20 extracts photoelectrons from extracellular sphalerite through cytochromes, nanowires, and electron shuttles. Genes encoding movement and biofilm formation are upregulated, suggesting that G20 might sense redox potential gradients and migrate towards sphalerite to acquire photoelectrons. This process enhances the intracellular electron transfer activity, sulphur metabolism, and ATP production of G20, which becomes dominant under conditions of carbon starvation and extends cell viability in such environments. This mechanism could be a vital strategy for SRMs to survive in energy-limited environments and contribute to sulphur cycling.

Rigorous Models for Vapor Diffusion in Polymers with Immobilization and Chemical Potential Gradients.

Two key phenomena─immobilization and concentration-dependent mixing free energies─simultaneously alter the sorption thermodynamics and diffusion of vapors in materials. This interrelation is leveraged to fit a unified model simultaneously capturing both sorption dynamics and the equilibrium isotherms. This transport model incorporates quasi-equilibrated immobilization reactions and considers Fick's law rigorously in terms of chemical potential gradients rather than concentration gradients. Five material case studies are discussed with varying characteristics, including fillers that provide sites for surface sorption, pores for capillary condensation, and apparent clustering or pooling at high vapor concentrations. Each case study illustrates that intrinsic diffusivity is constant, while the effective diffusivity changes predictably because of immobilization or changing free energies of mixing.

The regular octahedral CdS/K2Nb2O6 core-shell Z-Scheme heterojunction towards enhancing photocatalytic H2 evolution and degradation via synergism of carrier efficiency and light response

The regular octahedral CdS/K2Nb2O6 core-shell Z-Scheme heterojunction is synthesized via an approach of hydrothermal-chemical method. The CdS/K2Nb2O6 nano-heterojunction (CdS/KNO-3) exhibits arresting enhanced photocatalytic HER (∼634.39 μmol g−1 h−1)/degradation (∼0.05428 min−1) than the monomer K2Nb2O6 (∼27.8/14.4 folds) and CdS (∼20.3/10.0 folds), including a decent stability (average HER of ∼621.39 μmol∙g−1 h−1). It can be mainly attributed to the CdS/K2Nb2O6 Z-Scheme heterojunction with appropriate potential gradient can promote the interface carrier driving to optimize carrier efficiency, including increasing carrier transport, extending carrier lifetime and reducing recombination. Additionally, the octahedral core-shell nanostructure can provide numerous active sites for decreasing overpotential and promoting electron diffusion, while improving the solar efficiency (high solar response of CdS), including shorting carrier pathway for photocorrosion optimization and increasing structural stability.

A variational framework for Cahn–Hilliard-type diffusion coupled with Allen–Cahn-type multi-phase transformations in elastic and dissipative solids

This article presents a variational framework for coupled chemo-mechanical solids undergoing irreversible micro-structural changes at infinitesimal strains. The coupled problem is characterised by phenomena such as phase transitions, micro-structure coarsening and swelling. It is an extension of our previous work on variational inelasticity for a conserved chemo-mechanical setting to a unified conserved and non-conserved setting which include multi-phase transformations. The variational framework, again governed by continuous-time, discrete-time and discrete-space–time incremental variational principles, is outlined for coupled diffusion-phase transformation phenomena in elastic and dissipative solids. For the sake of simplicity, focus is restricted to isothermal conditions. It is shown that the governing macro- and micro-balance equations of the coupled problem appear as Euler equations of these minimisation and saddle point principles. In contrast to our previous work, extended variational principles (with the gradient of the chemical potential and phase fractions) are constructed that account for diffusion-phase transformation coupling. This is achieved by Legendre transformations. Note that the local–global solution strategy is still preserved and the resulting system of symmetric non-linear algebraic equations are solved by Newton–Raphson-type iterative methods. The applicability of the proposed framework is demonstrated by numerical simulations that qualitatively characterise lower bainitic micro-structure.

Stress heterogeneity in the eastern Tibetan Plateau and implications for the present-day plateau expansion

The eastward expansion of the Tibetan Plateau has resulted in different earthquake types in the eastern Tibetan Plateau, but the mechanism remains unclear. Here, we construct a three-dimensional visco-elastoplastic finite element model considering the topography to investigate the influence of fault geometry and rheological heterogeneity on stress fields. In our best-fitting model, the minimum principal stress is nearly vertical around the southern Huya fault zone, which is adjacent to the Longmen Shan fault zone, due to the significant mid-lower crust lateral rheological heterogeneity, and the thrust stress regime accounts for the reverse fault and thrust-dominated earthquakes. In this scenario, the eastward horizontal motion of the mid-lower crust is obstructed and facilitates thrust faulting, suggesting the limited eastward expansion of the Tibetan Plateau. In contrast, the northern Huya fault zone, one of the terminal branches of the East Kunlun fault, accommodates the continuous eastward extrusion of the East Kunlun fault, where the stress regime under a more homogenized crust favors the strike-slip faulting process, along with the dominant strike-slip earthquakes. Moreover, the best-fitting of stress regime explains the thrust-dominated 2008 Ms. 8.0 Wenchuan and 2013 Ms. 7.0 Lushan earthquakes on the Longmen Shan fault zone. Combining geophysical and geodetic observations and model analyses, we propose that the hybrid deformation mode in the eastern Tibetan Plateau is accommodated by upper crustal shear and thrusting deformation and mid-lower crustal thickening driven by the gravitational potential energy gradient. Our results elucidate the mechanism for differences in strong historical earthquakes and, more importantly, isolate the effect of fault geometry from those of heterogeneous viscosity on crustal deformation and stress heterogeneity in the eastern Tibetan Plateau.

Exploring the Effects of Fissures on Hydraulic Parameters in Subsurface Flows from the Perspective of Energy Changes

Reynolds number (Re), pore water pressure (P), and water flow shear force (τ) are primary indicators reflecting the characteristics of subsurface flow. Exploring the calculation of these parameters will facilitate the understanding of the hydrodynamic characteristics in different subsurface flows and quantify their differences. Hence, we conducted a study to monitor soil water content, matrix potential, and pore water pressure in two typical soil profiles (with and without fissures). The distribution of Re, P, and τ in both matrix flow (MF) and preferential flow (PF) were calculated with an improved calculation method, focusing on their energy changes. Results showed that these hydrologic parameters are quite different between MF and PF. Re values in MF remained below 0.1, indicating lower water flow velocities, while the Re values ranged from 0.8 to 2 in PF, indicating higher flow velocities. The P values in PF was tens to hundreds of times higher than that in MF, which is mainly due to the rapid accumulation and leakage of water within soil fissures. Additionally, the larger hydraulic radius and gradient in PF also resulted in higher τ values in PF (2~6 N m−2) than in MF (0~1.5 N m−2). In PF, the pressure potential was the significant factor for τ, while τ in MF was dominated by the matrix potential and varies with the magnitude of the matrix potential gradient. This study suggests that Re, P, and τ could be considered as the major indexes to reflect dynamic characteristics of subsurface flow.