Low Energy Research Articles

BLE Bluetooth remote-controlled car based on ESP32

Abstract. With the rapid advancement of information technology, Bluetooth technology has been widely used in the field of short-range wireless communication, playing an important role in information exchange. As one of the main technologies for short-range wireless communication, Bluetooth technology has broad application prospects, especially in robotic applications such as remote-controlled cars. This paper provides a detailed introduction to the design and implementation process of a Bluetooth remote-controlled car system based on the ESP32. It covers the classic Bluetooth and Bluetooth Low Energy (BLE) functionalities of the ESP32, the hardware design and assembly of the car (including the DC motor drive module, Bluetooth module, and speed measurement module), and methods for establishing a connection between the ESP32 and Bluetooth module, data transmission, and remote control of the car's movement. The paper also evaluates the system's performance through experiments, discusses the application and parameter adjustment of the PID control algorithm in enhancing speed control, and finally summarizes the research findings and suggests directions for future work.

Difluorobenzene as an Antisolvent for Fluorinated Electrolyte to Achieve Unparalleled Cycle Life of Lithium Metal Battery.

Electrolytes play a crucial role in enhancing the cycling stability and overall lifespan of lithium metal batteries (LMBs). However, conventional electrolytes achieve ununiform and low ionic conductivity solid electrolyte interphase (SEI), leading to uncontrolled lithium dendrite growth and dead lithium formation, rendering them inadequate for meeting the performance of high energy density LMBs. Herein, a 1,2-difluorobenzene (1,2-dFBn) is introduced as antisolvent in fluorinated electrolyte which is composed of fluoroethylene carbonate (FEC) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). The low energy level of the lowest unoccupied molecular orbital (LUMO) and the high fluorine-donating ability of 1,2-dFBn jointly modify the solvation structure and electrode/electrolyte interphase chemistry. As a result, this simple electrolyte formulation enables the Li||Li symmetric cells exhibit remarkable stability, enduring 700 h of continuous cycling under 2 mA cm-2 and Li||Cu cell achieve an impressive average Coulombic efficiency (CE) of 99.76%. Moreover, the full cell assembled with electrochemically deposited lithium capacity of 5 mAh cm-2 and LiFePO4 (LFP) as cathode achieves exceptional performance, maintaining a discharge specific capacity of 134.9 mAh g-1 while retaining 95.1% capacity at 2C after 1000 cycles. This study offers a plausible ratio design for fluorinated electrolyte, which achieving high CE and long-life LMBs.

Differential Positioning with Bluetooth Low Energy (BLE) Beacons for UAS Indoor Operations: Analysis and Results

Localization of unmanned aircraft systems (UASs) in indoor scenarios and GNSS-denied environments is a difficult problem, particularly in dynamic scenarios where traditional on-board equipment (such as LiDAR, radar, sonar, camera) may fail. In the framework of autonomous UAS missions, precise feedback on real-time aircraft position is very important, and several technologies alternative to GNSS-based approaches for UAS positioning in indoor navigation have been recently explored. In this paper, we propose a low-cost IPS for UAVs, based on Bluetooth low energy (BLE) beacons, which exploits the RSSI (received signal strength indicator) for distance estimation and positioning. Distance information from measured RSSI values can be degraded by multipath, reflection, and fading that cause unpredictable variability of the RSSI and may lead to poor-quality measurements. To enhance the accuracy of the position estimation, this work applies a differential distance correction (DDC) technique, similar to differential GNSS (DGNSS) and real-time kinematic (RTK) positioning. The method uses differential information from a reference station positioned at known coordinates to correct the position of the rover station. A mathematical model was established to analyze the relation between the RSSI and the distance from Bluetooth devices (Eddystone BLE beacons) placed in the indoor operation field. The master reference station was a Raspberry Pi 4 model B, and the rover (unknown target) was an Arduino Nano 33 BLE microcontroller, which was mounted on-board a UAV. Position estimation was achieved by trilateration, and the extended Kalman filter (EKF) was applied, considering the nonlinear propriety of beacon signals to correct data from noise, drift, and bias errors. Experimental results and system performance analysis show the feasibility of this methodology, as well as the reduction of position uncertainty obtained by the DCC technique.

Deterioration Patterns in Patients Admitted for Severe COPD Exacerbation

Background: Chronic obstructive pulmonary disease (COPD) exacerbations represent significant clinical events marked by worsening respiratory symptoms, often necessitating changes in medication or hospitalization. Identifying patterns of exacerbation and understanding their clinical implications are critical for improving patient outcomes. This study aimed to identify exacerbation patterns in COPD patients using variations in the COPD Assessment Test (CAT) scores and compare clinical characteristics and comorbidities among patients with different exacerbation patterns. Methods: An observational study was conducted involving COPD patients admitted for severe exacerbations. The administered CAT questionnaire referred to two periods: 1) the period during hospital admission and 2) the stable period two months prior to admission. Results: Fifty patients (60% male, mean age 70.5 years, standard deviation [SD] 9.6) were included; of these, eight (16%) were active smokers. Significant worsening in CAT scores during the exacerbation compared to the stable period was observed (25 vs. 13.5, p < 0.001). Three exacerbation patterns were identified: increased cough and sputum (cluster 1); increased dyspnea and activity limitation (cluster 2); and poorer sleep quality and lower energy (cluster 3). No significant differences were found regarding demographics and lung function. Conclusions: Three distinct exacerbation patterns were identified in COPD patients based on CAT score variations, suggesting that exacerbations are heterogeneous events. Future studies with larger sample sizes and prospective follow-up are necessary to validate these findings and explore their clinical and prognostic implications.

Superconductivity and nematic order in a new titanium-based kagome metal CsTi3Bi5 without charge density wave order

The cascade of correlated topological quantum states in the newly discovered vanadium-based kagome superconductors, AV3Sb5 (A = K, Rb, and Cs), with a Z2 topological band structure has sparked immense interest. Here, we report the discovery of superconductivity and electronic nematic order in high-quality single-crystals of a new titanium-based kagome metal, CsTi3Bi5, that preserves the translation symmetry, in stark contrast to the charge density wave superconductor AV3Sb5. Transport and magnetic susceptibility measurements show superconductivity with an onset superconducting transition temperature Tc of approximately 4.8 K. Using the scanning tunneling microscopy/spectroscopy and Josephson scanning tunneling spectroscopy, we demonstrate that the single crystals of CsTi3Bi5 exhibit two distinct superconducting gaps. Furthermore, the superconducting gaps break the six-fold crystal rotational symmetry down to two-fold. At low energies, we find that the quasiparticle interference patterns exhibit rotational-symmetry-breaking C2 patterns, revealing a nematic ordered normal state with the same nematic direction as in the superconducting state. Our findings uncover a novel superconducting state in CsTi3Bi5 and provide new insights for the intrinsic electron liquid crystal phases in kagome superconductors.

Tetrazaisoindigos:Serpentine Syntheses and Their Expected and Unexpected Photophysical and Electronic Properties.

Isoindigo, an electron-withdrawing building block for polymeric field-effect transistors, has long been considered to be non-fluorescent. Moreover, using electron-deficient heterocycle to replace the phenyl ring in the isoindigo core for better electron transport behaviour is synthetically challenging. Here we report the syntheses of a series of tetrazaisoindigos, including pyrazinoisoindigo (PyrII), pyrimidoisoindigo (PymII) and their hybrid (PyrPymII), and the investigation on their photophysical and electric properties. Proper flanking groups need to be chosen to stabilize these highly electron-deficient bislactams. Both PyrII and PymII derivatives show lower LUMO energy levels than that of naphthalene bisimide (NDI). Interestingly, PyrII is instinctively unstable and can be easily reduced, while both PymII derivatives are stable. More surprisingly, PymII derivatives are highly fluorescent and their photoluminescence quantum yields are around 40 %, 133 times higher than that of reported isoindigo derivatives. UV-vis spectroscopic results and theoretical calculations show that strong intramolecular hydrogen-bond exists in PymII, which prohibits it from non-radiative decay and accounts for its fluorescent behaviour. PymII derivatives are n-type semiconductors, while Ph-PyrII and the hybrid show balanced ambipolar charge transport behaviour, all among the best isoindigo derivatives. Our study not only discloses the structure-property relationship of tetrazaisoindigos, but also provides novel electron-deficient monomers for conjugated polymers.

Effect of non-additive mixing on entropic bonding strength and phase behavior of binary nanocrystal superlattices.

Non-additive mixing plays a key role in the properties of molecular fluids and solids. In this work, the potential for athermal order-disorder phase transitions is explored in non-additive binary colloidal nanoparticles that form substitutionally ordered compounds, namely, for equimolar mixtures of octahedra + spheres, which form a CsCl lattice compound, and cubes + spheres, which form a NaCl crystal. Monte Carlo simulations that target phase coexistence conditions were used to examine the effect on compound formation of varying degrees of negative non-additivity created by component size asymmetry and by size-tunable indentations in the polyhedra's facets, intended to allow the nestling of neighboring spheres. Our results indicate that the stabilization of the compound crystal requires a relatively large degree of negative non-additivity, which depends on particle geometry and the packing of the relevant phases. It is found that negative non-additivity can be achieved in mixtures of large spheres and small cubes having no indentations and lead to the athermal crystallization of the NaCl lattice. For similarly sized components, athermal congruent transitions are attainable and non-additivity can be generated through indentations, especially for the cubes + spheres system. Increasing indentation leads to lower phase coexistence free energy and pressure in the cubes + spheres system but has the opposite effect in the octahedra + spheres system. These results indicate a stronger stabilizing effect on the athermal compound phase by the cubes' indentations, where a deeper nestling of the spheres leads to a denser compound phase and a larger reduction in the associated pressure-volume free-energy term.

Mechanism of Inhibiting Spontaneous Coal Combustion by Dopa Hydrosol

ABSTRACT A new type of biomass environmentally friendly hydrosol (DEP) was proposed to inhibit coal spontaneous combustion (CSC). The DEP consists of two parts, the PDopa side chain solution formed by the redox reaction of Dopa and EGCG and the main chain sol solution formed by the free radical polymerization of AA under the action of APS initiator. The −COOH, −NH2, and −OH in Dopa can be grafted onto the skeleton of the main chain via double strong hydrogen bonding interactions with the −COOH group in PAA to form a stable three-dimensional cross-linked network structure. DEP can inhibit CSC through three aspects: oxygen isolation, increasing the activation energy of coal oxidation, scavenging active groups and free radicals. The calculation simulation results show that EGCG in DEP can remove various active free radicals with lower activation energy at room temperature, breaking the chain cycle reaction of coal spontaneous combustion, which proves its high efficiency. This study provides a new way to apply mussel-inspired adhesion mechanisms to the prevention of CSC.

Reducing Dead Species by Electrochemically-Densified Cathode-Interface-Reaction Layer towards High-Rate-Endurable Zn||I-Br Batteries.

Interhalogen-involved aqueous Zn||halogen batteries (AZHBs) are latent high-energy systems for grid-level energy storage, yet usually suffer from poor high-rate endurability caused by the formation of "dead species". Herein, via an electrochemically-densified cathode-interface-reaction layer (CIRL), Zn||I-Br batteries involving interhalogen reactions between the I2 cathode and Br- from the electrolytes are initially achieved with excellent high-rate endurability. Different from that in diluted electrolytes, the CIRL formed in Br--concentrated electrolyte is denser and water-lean, which enables halogen species conversion with a more rapid charge transfer and lower activation energy. More importantly, the CIRL robustly affords a decent I2 conservation by accelerated conversion kinetics and limited species diffusion, thereby endowing the Zn||I-Br batteries with an ultralong high-rate lifespan. The electrochemical mechanism is sufficiently verified by multiple spectral characterizations. Consequently, Zn||I-Br batteries in Br--concentrated (20 m) electrolytes exhibit an overwhelming rate capability and lifespan to those in Br--diluted (2 m) electrolytes. Typically, when cycled at a large current density of 10 A g-1, an ultralong lifespan of over 25,000 cycles is achieved with a high retention of 98.3%. This study provides new insight into the CIRL-dictated active species conservation for high-rate endurable AZHBs, which could apply to other high-energy interhalogen batteries.

Photovoltaic response promoted via intramolecular charge transfer in triphenylpyridine core with small acceptors: A DFT/TD-DFT study

Currently, A−π−A configured molecules (TTP1-TTP6) were designed from the reference compound (TPPR) by modifying the terminal acceptors for photovoltaic materials. Density functional theory (DFT) and time-dependent density functional theory (TD-DFT) using the M06/6-311G(d,p) functional were employed to analyze the photonic and electronic properties of the newly designed derivatives. Various analyses; frontier molecular orbitals (FMOs), density of states (DOS), absorption spectra (λmax), transition density matrix (TDM), binding energy (Eb), hole-electron and open circuit voltage (Voc) were performed to explore the photovoltaic properties of triphenylpyridine based compounds. The structural modulation with acceptor moieties significantly tuned their HOMO and LUMO levels, resulting in reduced band gaps (2.833–3.037 eV). They also exhibited broader absorption spectra (λmax) ranging from 482.560 to 514.756 nm as compared to the reference compound (486.289 nm). Notably, TPP3 showed the good photovoltaic response as it displayed the least energy gap (2.833 eV) with lower binding energy (0.415 eV) and bathochromic shift (512.798 nm) in absorption spectra as compared to all other derivatives. Beside this, a comparative study with spiro-OMeTAD and P3HT standard hole transport materials illustrated that these materials can also be utilized as effective photovoltaic materials.

Unlocking renewable fuel: Charcoal briquettes production from agro-industrial waste with cassava industrial binders

Increasing global fuel demand has created challenges in sourcing raw materials, making agro-waste biomass utilization for energy production a critical alternative. Therefore, the aim of this study was to investigate the production of charcoal briquettes using different base materials such as coconut shells (TC1), Leucaena leucocephala wood (TC2), and assorted wood charcoal residues (TC3), along with binders derived from cassava industry by-products—namely, tapioca starch (TB1), cassava peel (TB2), and cassava tubers (TB3) at binder content (BC) ratios of 5, 10, 15, and 20 by volume. Initially, assessing the physical properties, including proximate and ultimate analyses, was crucial for predicting effective charcoal production. The TC2 briquettes, using TB2 and TB3 binders at a BC20 concentration, were found to be optimal, displaying a high production capacity and low specific energy consumption. Using cassava peel and tubers as binders not only efficiently uses agricultural by-products, thereby reducing costs and avoiding competition with food resources (TC1) but also results in high-quality briquettes. In scenarios of raw material shortages, TC3 and TC2 can effectively replace TC1. Mechanically, TC3 and TC2 briquettes exhibited superior characteristics. Although BC20 enhances the mechanical properties and facilitates handling, it may compromise heat release. Thermally, a higher BC decreases the charcoal proportion, leading to increased ignition time, reduced calorific value, and heating effectiveness. In conclusion, the successful production of charcoal briquettes from agro-industrial waste using cassava industrial binders presents a viable pathway towards more sustainable energy practices, improves waste management, and adds value to agricultural waste.

Detection of a Planar Tetracoordinate Hydrogen within the Indium Framework by Quantum Dynamics Theory.

In this work, we consider the question how to detect the planar tetracoordination hydrogen geometry which was recently proposed by electronic structure calculations on the In4H+ system (Angew. Chem. Int. Ed. 2024, 63, e202317312; e202400927; e202403214). Keeping the C4v symmetry, a two-dimensional model of In4H+ is designed to build the nonadiabatic Hamiltonian operator with the lowest-lying singlet and triplet states coupled with spin-orbit coupling. The electronic energies in fitting the potential energy matrix are computed at either the MRCI or CCSD (T) level. Having constructed Hamiltonian, the multiconfigurational time-dependent Hartree product method predicts vibrational eigenstates for spectrum and recrossing probability of the proton. These quantum dynamics calculations predict a period of ∼60 fs for the proton recrossing the In4 moiety and further indicate that experimental observation of the D4h geometry for the triplet state is highly probable at room temperature even though the present MRCI and previous CASPT2 calculations (Angew. Chem. Int. Ed. 2024, 63, e202400927) both predict the C4v symmetry. To measure the C4v geometry, a low temperature of ≲30 K could be adopted. Despite the low temperature, the experiment might still miss the C4v geometry due to the nonzero recrossing probability of H at the low kinetic energy region. Further, a new type of hydrogen bonding in the D4h geometry is proposed to explain the interaction between the C4v geometries.

Significant Chiral Asymmetry Observed in Neutral Amino Acid Ultraviolet Photolysis.

The origin of homochirality in biological organisms remains an open question. Some suggest that its origin might be extraterrestrial, specifically due to the exposure of chiral molecules to circularly polarized photons in interstellar space, which could cause an initial population imbalance leading to the homochirality observed today. However, this extraterrestrial hypothesis has not been widely accepted, largely due to the belief that molecular optical rotatory dispersion is too insignificant to create the substantial imbalance required for homochirality. Here we report experimental evidence that specific conformers of neutral amino acids exhibit significant asymmetry in the chiral destroying dissociation rate induced by circularly polarized photons. The observed anisotropy factor for the lowest energy conformer of leucine was remarkably large, reaching 0.1─a factor of 13 times larger than observed for zwitterionic leucine in solid films, and nearly 40 times greater than the anisotropy reported in the electronic absorption spectrum of gas-phase leucine ensembles at room temperature. This significant finding indicates that even if reported anisotropy values in the electronic absorption spectrum are low, the dissociation asymmetry of certain conformers can still be substantial. An anisotropy factor of 0.1 could result in an initial enantiomeric excess exceeding 10%, even with a 90% extent of reaction. This discovery suggests that asymmetric photodissociation of amino acids may have been a crucial factor in the emergence of biological homochirality.

Self-assembled properties of water cuboids

Although liquid water and ice are characterised by predominantly tetrahedral coordination, small water clusters often exhibit a cubic structural motif. In this article, the stability of hydrogen-bonded water nanostructures in the form of n 1×n 2×n 3 cuboids is investigated. The requirement for complete hydrogen bonding imposes a strong constraint on their structure. The equations of the donor–acceptor balance are derived, from which all possible forms of completely hydrogen-bonded cuboids are deduced. The flexible non-additive AMOEBA potential is used for geometric optimisation of the set of configurations with different directions of hydrogen (H-) bonds. It has been established that the majority of completely hydrogen-bonded structures are formed by one layer of fused cubes. The lowest energy configurations of the, in fact, bilayer structures are formed by trans-configurations of transverse pairs of molecules, although some H-bonds are broken in this case. It is noted that the structure of the cuboids may result from the assembly of short nanotubes and smaller cuboids. On the other hand, unrealised H-bonds at the corners of the cuboids make it possible to assemble larger bilayer structures.

Controllability of optical, electrical, and magnetic properties of synthesized Cd-doped MgFe2O4 nanostructure

This study explores the synthesis of cadmium-magnesium co-doped magnesium ferrite (Mg1+xCdxFe2–2xO4, 0.00 ≤ x ≤ 0.30, Δx = 0.05) via a citric acid-assisted sol-gel auto-combustion method. X-ray diffraction (XRD) analysis revealed crystal structure changes due to Cd and Mg co-doping, with the 0.25 Cd sample showing the smallest crystallite size and highest lattice strain. High-resolution transmission electron microscopy (HRTEM) confirmed the nanostructure and largest surface area for this sample. Diffuse reflectance spectra, analyzed using the Kubelka-Munk relation, indicated that the 0.25 Cd sample had the lowest energy gap (2.08 eV), supported by band position calculations. Electrical conductivity and charge transport mechanisms were examined at various temperatures. Magnetization studies showed reduced saturation magnetization at x = 0.25, ascribed to cation distribution changes and spin canting, with coercivity and anisotropy decreasing with higher Cd content. Overall, the 0.25 Cd sample exhibited optimized optical, electrical, and magnetic properties due to its distinct microstructure.

Evaluating the antidiabetes and antioxidant activities of halogenated Schiff bases derived from 4-(diethylamino)salicylaldehyde: in vitro antidiabetes, antioxidant and computational investigation

Six Schiff bases with general name 5-(diethylamino)-2-(((halophenyl)imino)methyl)phenol (where halo = 4-fluoro (H1), 2-fluoro (H2), 2-bromo (H3), 4-bromo (H4), 4-chloro (H5) and 3-chloro-4-fluoro (H6)) were prepared by the condensation reaction between 4-(diethylamino)salicylaldehyde and suitable halogenated aromatic amines. The six halogenated Schiff bases were elucidated using different spectroscopic techniques and the structure of H3 and H6 were confirmed using single-crystal X-ray crystallography. The bond lengths of C7–N1, C7–C8 and C8–C9 obtained from structural analysis for both compounds depicted their enol-tautomeric characteristic form. The Hirshfeld analysis revealed that H‧‧‧H intermolecular contacts contributed most towards the Hirshfeld surfaces of both H3 (47.6%) and H6 (39.9%). Quantum chemical calculation studies showed that H1 and H2 have the highest and lowest energy band gap (∆E = 3.80 eV for H1 and ∆E = 3.73 eV for H2), depicting H2 and H1 as the most and least chemically reactive respectively among all the compounds. α-Amylase and α-glucosidase assay were used to evaluate the antidiabetes prowess of the synthesized compounds. All the compounds exhibited lower IC50 values than acarbose (reference drug) in α-amylase assay experiments and H5 with lowest IC50 value of 63.54 μM could be suggested to have the highest α-amylase inhibitory potential among the test samples. For α-glucosidase assay, H1–H6 displayed good antidiabetic potential. However, none of the compounds outshined acarbose with H6 having highest α-glucosidase inhibitory potential when compared to others i.e., IC50 of H6 = 60.89 μM and IC50 of acarbose = 51.42 μM. We measured the antioxidant potential of H1–H6 exploring 2,2-diphenyl-1-picrylhydrazyl (DPPH), nitric oxide (NO) and ferric reducing ability power (FRAP) assays. The DPPH as well as NO radical scavenging assay showed that all the compounds exhibited excellent antioxidant results with some of the compounds surpassing catechin (reference drug). Compound H5 with IC50 values of 30.32 mM and 31.73 mM outshined catechin with IC50 values of 31.17 mM and 140.62 mM for DPPH and NO assays respectively. All the compounds fell within the threshold of Lipinski’s Ro5 projecting them as orally bioavailable and less toxic future therapeutics.

Unlocking Full-Spectrum Brilliance: Dimensional Regulation in Lead-Free Metal Halides for Superior Photoluminescence.

Lead-free metal halides with tunable structures have emerged as a new class of optoelectronic materials. The arrangement of metal halide polyhedra defines their structural dimensionality and serves as a key factor influencing their optical properties. To investigate this, we synthesized four different antimony (Sb)-doped indium (In)-based metal halides, all of which possess zero-dimensional (0D) electronic structures but exhibit 3D, 2D, 1D, and 0D structural dimensionality at the molecular level. With a decreasing of structural dimensionality, their self-trapped exciton (STE) emission shows a red shift with peak position from 496 to 663 nm. We revealed that the red shift is caused by increased distortion of [SbCl6]3- octahedra as the structural dimensionality decreases, leading to lowered energy levels of STE and a corresponding red shift. The tunable STE emission makes these metal halides promising for anticounterfeiting and white LED applications. These findings provide a new strategy for tuning STE emission in lead-free metal halides.

Co-pyrolysis of rubber seed oil and industrial hemp stem: Asym2sig deconvolution, thermal behavior, synergistic reaction and kinetic

Evaluation of Kinetic triplets and thermodynamics of the co-pyrolysis of industrial hemp stem (IHS) and rubber seed oil (RSO) contributes to the efficient utilization of agricultural waste. The thermodynamics and kinetics of four pseudo components from mixture (RSO: IHS=1: 1) are investigated using Asym2sig deconvolution. The results show that the Eα of pseudo hemicellulose, pseudo cellulose, pseudo triglyceride and pseudo lignin are 76.019, 193.587, 231.764 and 408.552 kJ/mol. The average differences in Eα and ΔH for the four pseudo-fractions also are 4.439, 4.929, 5.576 and 6.018 kJ/mol. Lower energy barrier favors the reaction. The frequency factor values for four pseudo-components pyrolysis are 1.07 × 108 s−1 for pseudo hemicellulose, 1.78 × 1019 s−1 for pseudo cellulose, 6.04 × 1018 s−1 for pseudo triglyceride, and 6.96 × 1031 s−1 for pseudo lignin. The four pseudo-components have different pyrolysis reaction mechanisms. The synergistic effect calculations show a significant interaction between RSO and IHS. According to thermodynamic analysis, the pyrolysis of the four pseudo components requires the provision of external energy. FT-IR results indicate that RSO can significantly increase the release of C2H2, C2H4, C2H6 and CH4 during the co-pyrolysis of RSO and IHS. The co-pyrolysis of IHS and RSO can increase the content of alkene, alkane and MAHs, which improve the quality of bio-oil significantly. Besides, it can reduce the content of PAHs, which reduces the viscosity of the bio-oil. The results can provide new insights into the synergistic and efficient disposal of triglycerides and lignocellulosic biomass.

Interfacial Electric Field Enhanced Free-Standing VO2/rGO Aerogel Anode with Ultra High Mass Energy Density for Aqueous Ammonium Ion Battery.

Aqueous batteries have become a promising means of energy storage due to its environmental friendliness. Nevertheless, it often exhibits limited energy density that hinder their application. Considering that ammonium ion (NH4 +) has a low mass and a small hydration radius, aqueous ammonium ion batteries (AAIBs) are expected to solve the problem of low energy density. Herein, we obtain Vanadium dioxide/reduced graphene oxide aerogel (VOGA) by in-situ growth of VO2 on the graphene surface for interfacial electric field enhanced AAIBs to achieve high mass energy density. The VOGA free-standing electrode achieves a specific capacity of up to 655 mAg-1 at a current density of 0.5 Ag-1. And the mass energy density of the VOGA.

Optimization and energy management strategies, challenges, advances, and prospects in electric vehicles and their charging infrastructures: A comprehensive review

Electric vehicles (EVs) are at the forefront of global efforts to reduce greenhouse gas emissions and transition to sustainable energy systems. This review comprehensively examines the optimization and energy management strategies for EVs and their charging infrastructure, focusing on technological advancements, persistent challenges, and future prospects. By the end of 2023, the number of electric cars on the road globally reached 40 million, with 14 million new registrations recorded in 2023 alone—95% of which were in China, Europe, and the United States. Governments across the globe have introduced incentives and policies to promote EV adoption, and by 2030, EVs are expected to comprise a significant portion of light-duty vehicles in major regions. Despite these encouraging developments, challenges such as range anxiety, the relatively low energy density of 200–300 Wh/kg in Li-ion batteries (compared to 13,000 Wh/kg for petroleum), and insufficient public charging infrastructure remain key barriers to widespread EV adoption. This review also explores the critical role of smart grid technologies, vehicle-to-grid (V2G) systems, and renewable energy integration in supporting the growing EV market. V2G technologies are projected to enhance grid stability by 20–30% and reduce operational costs by 10–15% through load balancing and real-time energy price forecasting. By thoroughly analyzing optimization techniques such as load balancing, dynamic scheduling, and real-time energy management, this paper offers a roadmap for researchers, policymakers, and industry stakeholders to accelerate the integration of EVs into global energy systems and enhance sustainability in urban transportation networks.