Search Results (31)

Introduction: Huntington’s disease (HD) disrupts cortico-striato-thalamocortical circuits decades before clinical onset. Electroencephalography (EEG) offers millisecond temporal resolution, low cost, and broad accessibility, yet its mechanistic and biomarker potential in HD remains underexplored. We conducted a mechanistic review to synthesize half a century of EEG findings, identify reproducible electrophysiological signatures, and outline translational next steps. Methods: Two independent reviewers searched PubMed, Scopus, Google Scholar, ResearchGate, and the Cochrane Library (January 1970–April 2025) using the terms “EEG” OR “electroencephalography” AND “Huntington’s disease”. Clinical trials published in English that reported raw EEG (not ERP-only) in human HD gene carriers were eligible. Abstract/title screening, full-text appraisal, and cross-reference mining yielded 22 studies (~700 HD recordings, ~600 controls). We extracted sample characteristics, acquisition protocols, spectral/connectivity metrics, and neuroclinical correlations. Results: Across diverse platforms, a consistent spectral trajectory emerged: (i) presymptomatic carriers show a focal 7–9 Hz (low-alpha) power loss that scales with CAG repeat length; (ii) early-manifest patients exhibit widespread alpha attenuation, delta–theta excess, and a flattened anterior-posterior gradient; (iii) advanced disease is characterized by global slow-wave dominance and low-voltage tracings. Source-resolved studies reveal early alpha hypocoherence and progressive delta/high-beta hypersynchrony, microstate shifts (A/B ↑, C/D ↓), and rising omega complexity. These electrophysiological changes correlate with motor burden, cognitive slowing, sleep fragmentation, and neurovascular uncoupling, and achieve 80–90% diagnostic accuracy in shallow machine-learning pipelines. Conclusions: EEG offers a coherent, stage-sensitive window on HD pathophysiology—from early thalamocortical disinhibition to late network fragmentation—and fulfills key biomarker criteria. Translation now depends on large, longitudinal, multi-center cohorts with harmonized high-density protocols, rigorous artifact control, and linkage to clinical milestones. Such infrastructure will enable the qualification of alpha-band restoration, delta-band hypersynchrony, and neurovascular coupling as pharmacodynamic readouts, fostering precision monitoring and network-targeted therapy in Huntington’s disease. Full article

This study addresses the efficiency and cost challenges of hydrogen evolution reaction (HER) catalysts in the context of carbon neutrality strategies by employing a synergistic approach that combines cation vacancy anchoring and transition metal doping on two-dimensional (2D) MXenes. Using an in situ LiF/HCl etching process, the aluminum layers in Ti₃AlC₂ were precisely removed, resulting in a few-layer Ti₃C₂T_x MXene with an increased interlayer spacing of 12.3 Å. Doping with the transition metals Fe, Co, Ni, and Cu demonstrated that Fe@Ti₃C₂ provided the optimal HER performance, characterized by an overpotential (η₁₀) of 81 mV at 10 mA cm⁻², a low Tafel slope of 33.03 mV dec⁻¹, and the lowest charge transfer resistance (R_ct = 5.6 Ω cm²). Mechanistic investigations revealed that Fe’s 3d⁶ electrons induce an upward shift in the d-band center of MXene, improving hydrogen adsorption free energy and reducing lattice distortion. This research lays a solid foundation for the design of non-precious metal catalysts using MXenes and highlights future avenues in bimetallic synergy and scalability. Full article

Peroxymonosulfate (PMS)-based advanced oxidation technology has emerged as an effective means for removing organic pollutants from water due to its strong oxidizing ability. However, enhancing the activation efficiency of PMS represents a key challenge at present. SrTiO₃, a typical perovskite metal oxide, holds potential in the field of the photocatalytic degradation of pollutants, yet its application is limited by the wide bandgap and fast carrier recombination rates. This study optimized the photocatalytic performance of SrTiO₃ by regulating its electronic structure and optical properties through cobalt (Co) doping. Experimental results (TRPL, TPV, UV–Vis DRS, ESR, etc.) and DFT calculations (GGA-PBE) demonstrated that Co doping shifted the d-band center of SrTiO₃ upwards, optimized the adsorption energy of SO₄⁻, enhanced the sunlight response range, and significantly improved carrier extraction efficiency. Under visible light irradiation, 2,4-dichlorophenol (2,4-DCP) could be effectively degraded within 60 min in a wide pH range. Through Fukui function calculation (B3LYP/6-31G*) and experimental characterization analysis (HPLC-MS and IC), the possible degradation pathways of 2,4-DCP and the mechanism for photocatalysis were investigated. The toxicity analysis (T.E.S.T) confirmed the reduced toxicity of the degradation products of 2,4-DCPs. This study provides a reference for the catalyst design and optimization strategy of PMS-based advanced oxidation technology. Full article

In this study, nitrogen- and sulfur-co-doped MXene (NS-MXene) was developed as a high-performance cathode material for lithium–sulfur (Li-S) batteries. Heterocyclic Se₂S₆ molecules were successfully confined within the NS-MXene structure using a simple melt impregnation method. The resulting NS-MXene exhibited a unique wrinkled morphology with a stable structure which facilitated rapid ion transport and provided a physical barrier to mitigate the shuttle effect of polysulfide. The introduction of nitrogen and sulfur heteroatoms into the MXene structure not only shifted the Ti d-band center towards the Fermi level but also significantly polarizes the MXene, enhancing the conversion kinetics and ion diffusion capability while preventing the accumulation of Li₂S₆. Additionally, the incorporation of Se and S in Se₂S₆ improved the conductivity compared to S alone, resulting in reduced polarization and enhanced electrical properties. Consequently, NS-MXene/Se₂S₆ exhibited excellent cycling stability, high reversible capacity, and reliable performance at high current densities and under extreme conditions, such as high sulfur loading and low electrolyte-to-sulfur ratios. This work presents a simple and effective strategy for designing heteroatom-doped MXene materials, offering promising potential for the development of high-performance, long-lasting Li-S batteries for practical applications. Full article

The electrocatalysts of heteroatom-doped non-precious metal oxide materials are of great significance for efficient and low-cost electrochemical water-splitting systems. Herein, an innovative Fe-doped Co₃O₄ nanoflake (Fe-Co₃O₄/NF) on nickel foam has been developed, which exhibits excellent electrocatalytic activity for both hydrogen evolution reactions (HERs) and oxygen evolution reactions (OERs). Benefiting from the synergy of the charge redistribution and d-band center shift caused by doping engineering, the as-obtained Fe-Co₃O₄/NF shows both excellent HER (η₁₀ = 196 mV) and OER (η₁₀ = 290 mV) activities with low Tafel slopes (109 mV dec⁻¹ for HER and 49 mV dec⁻¹ for OER, respectively) and excellent stability. This work provides an effective method for designing and synthesizing bifunctional electrocatalysts with high activity and stability of metal oxide hybrids for the HER/OER. Full article

To better understand the hydrogen corrosion mechanism on uranium surfaces and assess the hydrogen penetration resistance of Al-U alloys, the adsorption of hydrogen atoms on U(110), Al(111), and nAl/U(110) alloy surfaces was systematically studied through density functional theory (DFT) calculations. The results reveal that when U is alloyed with Al, the adsorption behavior of H atom on its surface thereon changes greatly. Specifically, the adsorption energy of H decreases with increasing Al content, indicating a weakening of the interaction between the H atom and the surface. A correlation between binding strength and alloy composition was established using d-band center theory. The incorporation of Al atoms alters the electronic structure of the U(110) surface, shifting the d-band center of uranium atoms downward. This shift results in a weakened interaction between the adsorbed H atom and the alloy surface. Full article

Dry reforming of methane (DRM) is a promising way to convert methane and carbon dioxide into syngas, which can be further utilized to synthesize value-added chemicals. One of the main challenges for the DRM process is finding catalysts that are highly active and stable. This study explores the potential use of Ni-based catalysts modified by Ga. Different Ni-Ga/(Mg, Al)O_x catalysts, with various Ga/Ni molar ratios (0, 0.1, 0.3, 0.5, and 1), were synthesized by the co-precipitation method. The catalysts were tested for the DRM reaction to evaluate their activity and stability. The Ni/(Mg, Al)O_x and its Ga-modified Ni-Ga/(Mg, Al)O_x were characterized by N₂ adsorption–desorption, Fourier Transform Infrared Spectroscopy (FTIR), H₂-temperature-programmed reduction (TPR), X-ray diffraction (XRD), thermogravimetric analysis (TGA) and Raman techniques. The test of catalytic activity, at 700 °C, 1 atm, GHSV of 42,000 mL/h/g, and a CH₄: CO₂ ratio of 1, revealed that Ga incorporation effectively enhanced the catalyst stability. Particularly, the Ni-Ga/(Mg, Al)O_x catalyst with Ga/Ni ratio of 0.3 exhibited the best catalytic performance, with CH₄ and CO₂ conversions of 66% and 74%, respectively, and an H₂/CO ratio of 0.92. Furthermore, the CH₄ and CO₂ conversions increased from 34% and 46%, respectively, when testing at 600 °C, to 94% and 96% when the catalytic activity was operated at 850 °C. The best catalyst’s 20 h stream performance demonstrated its great stability. DFT analysis revealed an alteration in the electronic properties of nickel upon Ga incorporation, the d-band center of the Ga modified catalyst (Ga/Ni ratio of 0.3) shifted closer to the Fermi level, and a charge transfer from Ga to Ni atoms was observed. This research provides valuable insights into the development of Ga-modified catalysts and emphasizes their potential for efficient conversion of greenhouse gases into syngas. Full article

By controlling the structure and composition of Pt-based nanoalloys, the ethanol oxidation reaction (EOR) performances of Pt alloy catalysts can be effectively improved. Herein, we successfully synthesis sub-10 nm PdNi@PtNi nanoparticles (PdNi@PtNi NPs) with a core–shell structure by a one-pot method. The sub 10 nm core–shell nanoparticles possess more effective atoms and exhibit a synergistic effect which can lead to a shift in the d-band center and alter binding energies toward adsorbates. Due to the synergistic effect and unique core–shell structure, the PdNi@PtNi NP catalysts exhibit excellent electrocatalytic performance for ethanol oxidation reactions in alkaline, achieving 9.30 times more mass activity and 7.05 times more specific activity that of the state-of-the-art Pt/C catalysts. Moreover, the stability of PdNi@PtNi NPs was also greatly improved over PtNi nanoparticles, PtPd nanoparticles, and commercial Pt/C. This strategy provides a new idea for improving the electrocatalytic performance of Pt-based catalysts for EORs. Full article

Exploring highly active electrocatalysts as platinum (Pt) substitutes for the oxygen reduction reaction (ORR) remains a significant challenge. In this work, single Mn embedded nitrogen-doped graphene (MnN₄) with and without halogen ligands (F, Cl, Br, and I) modifying were systematically investigated by density functional theory (DFT) calculations. The calculated results indicated that these ligands can transform the d_yz and d_xz orbitals of Mn atom in MnN₄ near the Fermi-level into ${\mathit{d}}_{{\mathrm{z}}^2}$ orbital, and shift the d-band center away from the Fermi-level to reduce the adsorption capacity for reaction intermediates, thus enhancing the ORR catalytic activity of MnN₄. Notably, Br and I modified MnN₄ respectively with the lowest overpotentials of 0.41 and 0.39 V, possess superior ORR catalytic activity. This work is helpful for comprehensively understanding the ligand modification mechanism of single-atom catalysts and develops highly active ORR electrocatalysts. Full article

Weak doping can broaden, shift, and quench plasmon peaks in nanoparticles, but the mechanistic intricacies of the diverse responses to doping remain unclear. In this study, we used the time-dependent density functional theory (TD-DFT) to compute the excitation properties of transition-metal Pd- or Pt-doped gold and silver atomic arrays and investigate the evolution characteristics and response mechanisms of their plasmon peaks. The results demonstrated that the Pd or Pt doping of the off-centered 10 × 2 atomic arrays broadened or shifted the plasmon peaks to varying degrees. In particular, for Pd-doped 10 × 2 Au atomic arrays, the broadened plasmon peak significantly blueshifted, whereas a slight red shift was observed for Pt-doped arrays. For the 10 × 2 Ag atomic arrays, Pd doping caused almost no shift in the plasmon peak, whereas Pt doping caused a substantial red shift in the broadened plasmon peak. The analysis revealed that the diversity in these doping responses was related to the energy positions of the d electrons in the gold and silver atomic clusters and the positions of the doping atomic orbitals in the energy bands. The introduction of doping atoms altered the symmetry and gap size of the occupied and unoccupied orbitals, so multiple modes of single-particle transitions were involved in the excitation. An electron transfer analysis indicated a close correlation between excitation energy and the electron transfer of doping atoms. Finally, the differences in the symmetrically centered 11 × 2 doped atomic array were discussed using electron transfer analysis to validate the reliability of this analytical method. These findings elucidate the microscopic mechanisms of the evolution of plasmon peaks in doped atomic clusters and provide new insights into the rational control and application of plasmons in low-dimensional nanostructures. Full article

Transition metal (TM) single-atom catalysts (SACs) have been widely applied in photocatalytic CO₂ reduction. In this work, n–p codoping engineering is introduced to account for the modulation of photocatalytic CO₂ reduction on a two-dimensional (2D) bismuth-oxyhalide-based cathode by using first-principles calculation. n–p codoping is established via the Coulomb interactions between the negatively charged TM SACs and the positively charged Cl vacancy (V_Cl) in the dopant–defect pairs. Based on the formation energy of charged defects, neutral dopant–defect pairs for the Fe, Co, and Ni SACs (P_TM⁰) and the −1e charge state of the Cu SAC-based pair (P_Cu⁻¹) are stable. The electrostatic attraction of the n–p codoping strengthens the stability and solubility of TM SACs by neutralizing the oppositely charged V_Cl defect and TM dopant. The n–p codoping stabilizes the electron accumulation around the TM SACs. Accumulated electrons modify the d-orbital alignment and shift the d-band center toward the Fermi level, enhancing the reducing capacity of TM SACs based on the d-band theory. Besides the electrostatic attraction of the n–p codoping, the P_Cu⁻¹ also accumulates additional electrons surrounding Cu SACs and forms a half-occupied d_x²_−y² state, which further upshifts the d-band center and improves photocatalytic CO₂ reduction. The metastability of Cl multivacancies limits the concentration of the n–p pairs with Cl multivacancies (P_TM@nCl (n > 1)). Positively charged centers around the P_TM@nCl (n > 1) hinders the CO₂ reduction by shielding the charge transfer to the CO₂ molecule. Full article

This paper presents a compact wideband circularly polarized cross-dipole antenna with a low-pass filter response. It consists of two pairs of folded cross-dipole arms printed separately on both sides of the top substrate, and the two dipole arms on the same surface are connected by an annular phase-shifting delay line to generate circular polarization. A bent metal square ring and four small metal square rings around the cross-dipoles are employed to introduce new resonant frequencies, effectively extending the impedance and axial-ratio bandwidth. Four square patches printed on the middle substrate are connected to the ground plane by the vertical metal plates in order to reduce the antenna height. Thus, a compact wideband circularly polarized antenna is realized. In addition, a transmission zero can be introduced at the upper frequency stopband by the bent metal square rings, without using extra filter circuits. For verification, the proposed model is implemented and tested. The overall size of the model is $90\mathrm{mm}\times 90\mathrm{mm}\times 33\mathrm{mm}$ ($0.37{\lambda }_0\times 0.37{\lambda }_0\times 0.14{\lambda }_0$; ${\lambda }_0$ denotes the center operating frequency). The measured impedance bandwidth and 3 dB axial-ratio (AR) bandwidth are 53.3% and 41%, respectively. An upper-band radiation suppression level greater than 15 dB is realized, indicating a good low-pass filter response. Full article

Zero-dimensional (0D) tin halide perovskites, characterized by their broadband and adjustable emissions, high photoluminescence quantum yield, and absence of self-absorption, are crucial for the fabrication of high-efficiency optoelectronic devices, such as LEDs, solar cells, and sensors. Despite these attributes, boosting their emission efficiency and stability poses a significant challenge. In this work, Cr³⁺-doped Cs₄SnBr_6−xF_x perovskites were synthesized using a water-assisted wet ball-milling method. The effect of CrF₃ addition on photoluminescence properties of Cs₄SnBr_6−xF_x Perovskites was investigated. We found that Cr³⁺-doped Cs₄SnBr_6−xF_x Perovskites exhibit a broad emission band, a substantial Stokes shift, and an efficient green light emission centered at about 525 nm at ambient temperature. The derived photoluminescence quantum yield amounted to as high as 56.3%. In addition, these Cr³⁺-doped Cs₄SnBr_6−xF_x perovskites outperform their undoped counterparts in terms of thermal stability. Through a comprehensive analysis of photoluminescence measurements, our findings suggested that the elevated photoluminescence quantum yield can be attributed to the enhanced exciton binding energy of self-trapped excitons (STEs) and the suitable electron−phonon coupling resulting from the substantial distortion of [SnBr₆]⁴⁻ octahedra instigated by the addition of CrF₃. Full article

Ethylene is an ideal CO₂ product in an electrocatalytic CO₂ reduction reaction (CO₂RR) with high economic value. This paper synthesised Al-doped octahedral Cu₂O (Al–Cu₂O) nanocrystal by a simple wet chemical method. The selectivity of CO₂RR products was improved by doping Al onto the surface of octahedral Cu₂O. The Al–Cu₂O was used as an efficient electrocatalyst for CO₂RR with selective ethylene production. The Al–Cu₂O exhibited a high % Faradic efficiency (FE_C2H4) of 44.9% at −1.23 V (vs. RHE) in CO₂ saturated 0.1 M KHCO₃ electrolyte. Charge transfer from the Al atom to the Cu atom occurs after Al doping in Cu₂O, optimizing the electronic structure and facilitating CO₂RR to ethylene production. The DFT calculation showed that the Al–Cu₂O catalyst could effectively reduce the adsorption energy of the *CHCOH intermediate and promote the mass transfer of charges, thus improving the FE_C2H4. After Al doping into Cu₂O, the center of d orbitals shift positively, which makes the d–band closer to the Fermi level. Furthermore, the density of electronic states increases due to the interaction between Cu atoms and intermediates, thus accelerating the electrochemical CO₂ reduction process. This work proved that the metal doping strategy can effectively improve the catalytic properties of Cu₂O, thus providing a useful way for CO₂ cycling and green production of C₂H₄. Full article

This paper presents a new design for a 1 × 4 optical power splitter using multimode interference (MMI) coupler in silicon nitride (Si₃N₄) strip waveguide structures. The main functionality of the proposed design is to use Si₃N₄ for dealing with the back reflection (BR) effect that usually happens in silicon (Si) MMI devices due to the self-imaging effect and the higher index contrast between Si and silicon dioxide (SiO₂). The optimal device parameters were determined through numerical optimizations using the beam propagation method (BPM) and finite difference time domain (FDTD). Results demonstrate that the power splitter with a length of 34.6 μm can reach equal distribution power in each output port up to 24.3% of the total power across the O-band spectrum with 0.13 dB insertion loss and good tolerance MMI coupler parameters with a shift of ±250 nm. Additionally, the back reflection range over the O-band was found to be 40.25–42.44 dB. This demonstrates the effectiveness of the incorporation using Si₃N₄ MMI and adiabatic input and output tapers in mitigating unwanted BR to ensure that a good signal is received from the laser. This design showcases the significant potential for data-center networks, offering a promising solution for efficient signal distribution and facilitating high-performance and reliable optical signal routing within the O-band range. By leveraging the advantages of Si₃N₄ and the MMI coupler, this design opens possibilities for advanced optical network architectures and enables efficient transmission of optical signals in the O-band range. Full article