Interfacial Charge Transfer Research Articles

Building Asymmetric Zn–N3 Bridge between 2D Photocatalyst and Co‐catalyst for Directed Charge Transfer toward Efficient H2O2 Synthesis

Two‐dimensional (2D) polymeric semiconductors are a class of promising photocatalysts; however, it remains challenging to facilitate their interlayer charge transfer for suppressed in‐plane charge recombination and thus improved quantum efficiency. Although some strategies, such as π‐π stacking and van der Waals interaction, have been developed so far, directed interlayer charge transfer still cannot be achieved. Herein, we report a strategy of forming asymmetric Zn–N3 units that can bridge nitrogen (N)‐doped carbon layers with polymeric carbon nitride nanosheets (C3N4‐Zn‐N(C)) to address this challenge. The symmetry‐breaking Zn–N3 moiety, which has an asymmetric local charge distribution, enables directed interfacial charge transfer between the C3N4 photocatalyst and the N‐doped carbon co‐catalyst. As evidenced by femtosecond transient absorption spectroscopy, charge separation can be significantly enhanced by the interfacial asymmetric Zn–N3 bonding bridges. As a result, the designed C3N4‐Zn‐N(C) catalyst exhibits dramatically enhanced H2O2 photosynthesis activity, outperforming most of the reported C3N4‐based catalysts. This work highlights the importance of tailoring interfacial chemical bonding channels in polymeric photocatalysts at the molecular level to achieve effective spatial charge separation.

Needle growth of Nb2O5 nanoparticles on BiOCl nanosheets to fabricate S-scheme heterojunction with oxygen vacancies for enhanced photooxidation of cyclohexane

The exploration of cost-efficient, environmentally friendly, and high-efficacy photocatalysts for the enhanced selective photooxidation of cyclohexane to KA oil (cyclohexanone (CHA-one) and cyclohexanol (CHA-ol)) is a pivotal challenge in the industrial realm. Herein, the present study focuses on the synthesis of needle-like S-scheme heterojunction photocatalysts with oxygen vacancies, which are achieved by the needle growth integration of nano-sized Nb2O5 particles onto the BiOCl nanosheets. Remarkably, the 40 % Nb2O5/BiOCl composites exhibited superior performance in the solvent-free photooxidation of cyclohexane at room-temperature and under atmospheric pressure. The production yield of KA oil was 180.3 μmol (CHA-one/CHA-ol molar ratio = 3.5), and exceptional selectivity towards KA oil, reaching up to 99.3 %. The enhanced photocatalytic efficiency in cyclohexane oxidation can be attributed to the unique S-scheme heterogeneous interfaces with specific nanoneedle morphology, which result in the enhanced photonic absorption, effective charge carrier separation, a high density of oxygen vacancies, and the exposure of the highly reactive (001) plane of BiOCl. The excellent interfacial charge separation and transfer pathways of S-scheme heterojunction are disclosed by the in-depth EPR analysis and DFT calculations. These insights highlight the significant potential of the needle-like Bi-based S-scheme heterojunction photocatalysts for the efficient photooxidation of saturated alkanes.

Dual-defect AgBiO3/DCN S-scheme heterojunction for booted photocatalytic removal of Norfloxacin: Interfacial charge transfer, mechanism and toxicity assessment insights

Antibiotics pollution may pose a great risk to ecosystem and human health. In this work, an innovative dual-defect AgBiO3/DCN S-scheme heterojunction was constructed to overcome the sluggish charge separation and transfer issue and showed exceptional photodegradation performance towards norfloxacin (NFL) pollution under the visible light. The degradation efficiency of NFL reached 95.30 % within 120 min respectively, the rate constant was 3.64 times higher than that of defective g-C3N4 (DCN). The systematically characterizations proved that the enhanced photocatalytic activity was benefited from optimized band structures, improved carrier separation efficiency, due to dual defects and S-scheme heterojunction in AgBiO3/DCN. the intermediate degradation products and degradation pathway of NFL were speculated by UPLC-HRMS, and the environmental toxicity degree of degradation products was analyzed according to the T.E.S.T software. The charge transfer pathway was confirmed as an S-scheme mechanism through a combination of band structure analysis, alongside electron paramagnetic resonance (EPR) experiments.The quenching experiments and ESR analyses indicated that h+ and O2•− radicals played predominant roles. The efficient and stable photocatalytic NFL degradation efficiency and broad environmental adaptability proved potential practical application. This work may shed light on designing new dual-defect heterojunction with photocatalytic antibiotic removal capability in the innovative water treatment process.

Electrochemical detection of human papillomavirus DNA based on an ultrasensitive electrochemical sensing platform using N-graphene paper

Human papillomavirus (HPV) is the primary cause of cervical cancer, a major global health concern affecting women worldwide. Early detection of high-risk HPV genotypes is crucial for timely intervention and reducing disease burden. However, current detection methods often lack sensitivity, speed, or cost-effectiveness, especially in resource-limited settings. This work addresses this critical need by developing an ultrasensitive electrochemical biosensing platform based on nitrogen-doped graphene paper electrodes for quantifying high-risk HPV16 DNA sequences. The N-graphene nanohybrid, fabricated via simple solvothermal treatment of biomass-derived graphene oxide, demonstrated significantly enhanced electrical and electrocatalytic properties compared to undoped graphene. DNA detection was achieved through characteristic oxidation signals of guanine bases, which displayed a wide linear dynamic range (0.5–100 μg/mL), low detection limit (75 pg/mL), and excellent reproducibility (relative standard deviation <3.5 %). Detailed spectroscopic and electrochemical analyses revealed the key roles of pyridinic nitrogen defects in improving interfacial charge transfer kinetics and mitigating biofouling issues. This synergistic combination of high electrical conductivity and versatile surface functionality paves the way for equipment-free, point-of-care genosensor devices tailored for quantitative biomarker screening in resource-constrained environments.

Toward the Rechargeable Aqueous Zinc Ion Batteries with Improved Overall Performance: Electrolyte with Surface Adsorptive Additive.

Aqueous zinc-ion batteries (AZIBs) with slightly acidic electrolytes process advantages such as high safety, competitive cost, and satisfactory electrochemical performance. However, the failure behaviors of both electrodes, regarding zinc dendrite growth, interfacial parasitic reactions, and the collapse of cathode materials hinder the practical application of ZIBs. To alleviate the issues of both anode and cathode at the same time, D-xylose (DX) is introduced to the electrolyte as a multifunctional additive. As a result, the side reaction of the anode is suppressed and the metallic deposition behavior is regulated due to the hydrogen bonding network reconstruction and preferential surface adsorption of DX; for the MnO2 cathode, the DX adsorption can help the interfacial charge transfer and increase the reactive sites. Benefiting from these merits, DX-optimized Zn//Zn battery displays reveal a prolonged lifespan of 6912h and an ultra-high cumulative capacity of 17.28Ahcm-2 at 5mAcm-2. With the function of water reactivity suppression, the Coulombic efficiency reaches 99.91% at 2mAcm-2; the Zn||MnO2 full batteries exhibit excellent cyclability over 2000 cycles at 5C with an increased capacity of 118.9mAhg-1, indicating the dual functions to both of the electrodes for AZIBs.

Ultra-sensitive zinc cobaltate assembled on N-rich carbon nitride electrochemical sensor for the detection of paraquat in food samples

BackgroundParaquat (PQ) from agricultural waste cause contamination in water bodies, groundwater, soil, and foods has received increasing attention regarding health safety. On-site-based detection is much needed along with rapid results, selectivity and sensitivity, which can be achieved through an electrochemical-based sensor. MethodsThis work provides, an electrochemical sensor based on zinc cobaltite (ZnCo2O4) nanostructure strongly attracted through electrostatic interaction with the carbon nitride (C3N5; CN) nanosheets modified on a glassy carbon electrode (GCE) for the determination of paraquat (PQ). The strong immobilization of ZnCo2O4 over CN2 on GCE synergistically shows excellent sensing of PQ due to high interfacial charge transfer effect. Significant findingsIn addition, the electrochemical studies were performed using CV and DPV analysis which exhibits a good limit of detection (7.6 nM) and sensitivity (0.201 µA cm-2) towards PQ detection. Furthermore, the modified electrode was applied practically in real food samples for PQ detection with excellent recoveries.

Unraveling the Spin-to-Charge Current Conversion Mechanism and Charge Transfer Dynamics at the Interface of Graphene/WS2 Heterostructures at Room Temperature.

We report experimental investigations of spin-to-charge current conversion and charge transfer (CT) dynamics at the interface of the graphene/WS2 van der Waals heterostructure. Pure spin current was produced by the spin precession in the microwave-driven ferromagnetic resonance of a permalloy film (Py=Ni81Fe19) and injected into the graphene/WS2 heterostructure through a spin pumping process. The observed spin-to-charge current conversion in the heterostructure is attributed to the inverse Rashba-Edelstein effect (IREE) at the graphene/WS2 interface. Interfacial CT dynamics in this heterostructure was investigated based on the framework of the core-hole clock (CHC) approach. The results obtained from spin pumping and CHC studies show that the spin-to-charge current conversion and charge transfer processes are more efficient in the graphene/WS2 heterostructure compared to isolated WS2 and graphene films. The results show that the presence of WS2 flakes improves the current conversion efficiency. These experimental results are corroborated by density functional theory (DFT) calculations, which reveal (i) Rashba spin-orbit splitting of graphene orbitals and (ii) electronic coupling between graphene and WS2 orbitals. This study provides valuable insights for optimizing the design and performance of spintronic devices.

Electrostatic Gating-Dependent Multiple Band Alignments in Ferroelectric α-In2Se3/α-Te van der Waals Heterostructures.

The two-dimensional ferroelectric van der Waals (vdW) heterojunction has been recognized as one of the most promising combinations for emerging ferroelectric memory materials due to its noncovalent bonding and flexible stacking of various materials. In this work, the first-principles calculations were performed to study the stable geometry and electronic structure of α-In2Se3/α-Te, incorporating the vdW correction via the DFT-D2 method. The reversal of the polarization direction in α-In2Se3 can induce a transition in the heterostructure from metallic to semiconductor, accompanied by a shift from type-III to type-I band alignment. These changes are attributed to variations in interfacial charge transfer. Analysis of the modulation effects of external electric fields reveals that the P↑ α-In2Se3/α-Te configuration maintains metallic, whereas the P↓ α-In2Se3/α-Te configuration exhibits a linear reduction in band gap. Furthermore, both heterostructural configurations will undergo transitions to type-II band alignment transitions at 0.2 V Å-1 and within a range from 0.2 to 0.3 V Å-1 under external electric fields. Our findings offer valuable insights for applications such as ferroelectric memory and static gate devices with multiband alignment.

Z-scheme heterostructures confining rGO/protonated C3N5 junction supported CoCu LDH positive electrode and Fe3O4 negative electrode for supercapacitors

CoCu LDH stabilized reduced graphene oxide-linked N-rich protonated C3N5 (CoxCuy@rGO/P-CN) as a power source Z-scheme nanocomposite was rationally tailored engineered an electrodeposition approach. The electrochemical performance was regulated by adjusting the electrodeposition potential and manipulating the Co/Cu molar ratio. Hence, affording compelling evidence for fine-tuning the performance of pseudo-active compounds. Benefiting from abundant heterointerfaces and synergistic effects between LDH nanoarrays and rGO/P-CN heterojunction, the hierarchical ‒1.2V Co3Cu1@rGO/P-CN Z-scheme positive electrode achieves a higher capacitance of 1184 F g–1 at 1 A g–1 and good rate capability performance. Theoretical simulation outcomes illustrate that the Co3Cu1@rGO/P-CN nanocomposite has higher electronic conductivity and superior electronic transition capability, originating from robust interactions between valence and conduction bands, interfacial charge transfer, and built-in electric field at the LDH/rGO/P-CN interface. We also explore the Fe3O4@rGO/P-CN Z-scheme as a negative electrode material via a simple annealing process with a capacitance of 402 F g–1 at 1 A g–1 and an enhanced cyclic performance. Consequently, the as-assembled ‒1.2V Co3Cu1@rGO/P-CN//Fe3O4@rGO/P-CN asymmetric supercapacitor (ASC) cell acquires a remarkable energy density of 63.4 Wh kg–1 at 750 W kg–1 and displays an exceptional cycling activity with 88% retention after 11,000 cycles.

In Situ Driven Formation of Anatase/Brookite/Rutile Heterojunction N/TiO2 Nanocrystals as Sustainable Visible-Light Catalysts.

Visible-light active anatase/brookite/rutile (A/B/R) ternary N-doped titania (N/TiO2) crystals are successfully prepared by a facile sol-gel method using titanium butoxide and benign N-dopant source, guanidinium chloride. Systematically varying the aging time (1, 4, 8, and 12 d), its influence on physicochemical properties of as-obtained spherical heterojunction nanomaterials is studied. Detailed characterizations confirm that a substantial amount of anatase (88% to 50%) is transformed to rutile (2% to 38%) via intermediate brookite phase (9% to 25%) as the function of aging time; not only the A/B/R phase content of the samples is tuned by sol-gel aging time of the precursors solution but also their optical-response and methylene blue photocatalytic properties are profoundly dictated. Notably under visible-light irradiation, the photostable rutile rich mesoporous A/B/R triphasic N/TiO2 (50% A, 12% B, 38% R) aged for 12 d demonstrates higher degradation activity (97%) with a faster degradation rate (0.033 min-1) than both lesser aged N/TiO2 and undoped titania. This enhancement is attributed to the synergistic effect of interstitial-N-doping and optimal A/B/R interfacial charge transfer that leads to higher light absorption, lower bandgap energy and well-separated charge carriers. The current work provides a new perspective for designing highly active visible-light heterostructure nanomaterials with controllable phase composition.

Enhanced Interface Charge Transfer through Heterostructure Coupling of NiO/NiCo2O4 and Carbon Layer for Photocatalysis

Constructing heterogeneous composite materials is a promising strategy for enhancing photocatalytic performance. In this study, the calcination method was employed to coat a carbon layer onto the surface of quartz sand. Additionally, NiO/NiCo2O4 heterostructures were loaded onto the carbon layer to facilitate charge transfer and enhance photo-generated electron yield. The carefully designed QSC@NiO/NiCo2O4 heterojunction possesses an efficient interface charge transfer channel, thereby improving contaminant degradation capacity. The results demonstrated that under 120 minutes of light exposure, the removal efficiencies for RhB and MB reached 94.75% and 93.55%, respectively. After undergoing 5 cycles, both RhB and MB exhibited consistently high elimination rates with values of 83.74% and 77.42%, respectively. Furthermore, tapping experiments were conducted to explore the mechanism of photocatalytic degradation.

Advancements in Rechargeable Zn-Air Batteries with Transition-Metal Dichalcogenides as Bifunctional Electrocatalyst.

This review covers recent progress on transition metal dichalcogenides (TMDs) as bifunctional electrocatalysts for Zinc-air batteries (ZABs), emphasizing their suitable surface area, electrocatalytic active sites, stability in acidic/basic environments, and tunable electronic properties. It discusses strategies like defect engineering, doping, interface, and structural modifications of TMDs nanostructures for enhancing the performances of ZABs. Zinc-air batteries are promising energy storage devices owing to their high energy density, low cost, and environmental friendliness. However, the development of durable and efficient bifunctional electrocatalysts is a major concern for Zn-air batteries. In this review, we summarize the recent progress on transition metal dichalcogenides (TMDs) as bifunctional electrocatalysts for Zn-air batteries. We discuss the advantages of TMDs, such as high activity, good stability, and tunable electronic structure, as well as the challenges, such as low conductivity, poor durability, and limited active sites. We also highlight the strategies for fine-tuning the properties of TMDs, such as defect engineering, doping, hybridization, and structural engineering, to enhance their catalytic performance and stability. We provide a comprehensive and in-depth analysis of the applications of TMDs in Zn-air batteries, demonstrating their potential as low-cost, abundant, and environmentally friendly alternatives to noble metal catalysts. We also suggest future directions like exploring new TMDs materials and compositions, developing novel synthesis and modification techniques, investigating the interfacial interactions and charge transfer processes, and integrating TMDs with other functional materials. This review aims to illuminate the path forward for the development of efficient and durable Zn-air batteries, aligning with the broader objectives of sustainable energy solutions.

Construction of magnetically separable S-scheme BiFeO3/Cl-g-C3N4 heterostructure photocatalyst for simultaneous removal of Cr(Ⅵ) and tetracycline in aqueous solution: Performance and mechanism insight

A green, efficient and recyclable magnetic BiFeO3/Cl-g-C3N4 photocatalyst was prepared for the simultaneous removal of Cr(Ⅵ) and tetracycline (TC) from water by wet chemical and thermal synthesis methods. Experimental results revealed that BiFeO3/Cl-g-C3N4 achieved a removal efficiency of 96.1 % for Cr(Ⅵ) and 98.2 % for TC under visible light irradiation for 50 min at pH 6. The results of the work function, differential charge density, UV–vis DRS, PL, PC and EIS tests indicate the formation of S-scheme heterojunctions between BiFeO3 and Cl-g-C3N4, which exhibits superior carrier separation and migration efficiency. The evidence for interfacial charge transfer from BiFeO3 to Cl-g-C3N4 within BiFeO3/Cl-g-C3N4 was further corroborated by means of ISIXPS, EPR and KPFM. Moreover, calculations of the density of states demonstrate that the introduction of Cl enhances the reduction capability of BiFeO3/Cl-g-C3N4. Results from ESR tests and trapping experiments has demonstrated that the singlet oxygen (1O2) and electrons are the primary active species. Furthermore, the high removal rates of TC and Cr(VI) from industrial wastewater and groundwater, coupled with the lower ecotoxicity of TC degradation intermediates, indicate that BiFeO3/Cl-g-C3N4 has the potential for practical applications. After five cycles, the BiFeO3/Cl-g-C3N4 still removed 90.5 % of TC and 96 % of Cr(Ⅵ).

Fe3O4 encapsulated in hierarchically porous nitrogen-doped graphitic carbon layers for efficient oxygen reduction reaction: Enhanced intrinsic activity via directional interfacial charge transfer

Constructing efficient electrocatalysts for the oxygen reduction reaction (ORR) is crucial for the commercialization of metal-air batteries. Iron oxide-based catalysts exhibit promising potential for ORR. However, addressing the issue of inferior catalytic performance is essential, and a comprehensive understanding of the catalytic mechanism of iron oxide-based catalysts is also lacking. In this study, we present Fe3O4 nanoparticles encapsulated in N-doped graphitic carbon layers (NGC) hosted by hierarchically porous carbon (Fe3O4@NGC), achieved through a facile dual melt-salt template strategy. The encapsulation of Fe3O4 nanoparticles protects them from corrosion and exfoliation, endowing the catalysts with superior stability. Density functional theory (DFT) calculations discover that the electronic interaction between Fe3O4 nanoparticles and N-doped graphitic carbon layers induces directional interfacial electron transfer, which effectively modulates the surface electronic structure to improve the binding ability to O2, weaken the OO bond, and optimize the adsorption of intermediates, thus boosting the intrinsic activity. DFT unveils that the C atoms nearest to graphitic-N in NGC are active sites. Finally, the synergistic effects of Fe3O4 nanoparticles and NGC result in outstanding ORR performance and superior stability and methanol tolerance of Fe3O4@NGC, with a half-wave potential of 0.89 V, surpassing that of Pt/C by 50 mV. Fe3O4@NGC also shows better performance than Pt/C when used as the air-electrode catalyst in zinc-air battery.

Interface-engineered Ni(Fe/Al)-LDHs/g-C3N4 nanosheets with metallic Fe/Al[sbnd]N bonds for efficient photocatalytic degradation of tetracycline hydrochloride

To improve the photogenerated electron–hole separation efficiency and the number of reactive oxygen species of g-C3N4 in visible light. Herein, an interface-engineered Ni(Fe/Al)-LDHs/g-C3N4 nanosheets with Fe/AlN bonds were prepared, which shows highly enhanced photocatalytic degradation performance with excellent structural stability. The interfacial structure of g-C3N4 was precisely regulated by metal Fe/Al on the surface of layered double hydroxides (LDHs), which could form Fe/AlN bonds as the interfacial charge transfer channels. In addition, the metal Ni and Fe/Al on the surface of LDHs nanosheets can furnish more photocatalytic active sites and interface synergy. The obtained 7 %NiFe-LDHs/g-C3N4 owns the degradation rate of 99.23 % for tetracycline hydrochloride (TCH) in visible light. This work highlights a rational interface engineering strategy for the formation of a composite structure with interface interaction for efficient photocatalysts.

Ultra-fine carbon decorated TiO2/C/g-C3N4 hybrid for strong physical adsorption and efficient photodegradation of pollutants

Enhancement in the visible light absorption and efficient interfacial charge transfer is crucial for optimizing photocatalytic efficiency in the degradation of pollutants such as methyl orange (MO) and formaldehyde. This study focuses on the properties of a TiO2/C/g-C3N4 hybrid efficient photocatalyst is developed by employing an air calcination method to deposit graphitic nitride (g-C3N4) onto a carbon-modified TiO2 surface. The characterization techniques, including high-resolution transmission electron Microscopy (HRTEM), X-ray diffraction (XRD), Raman spectroscopy, thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS), were used to provide a comprehensive understanding of the material’s structural, morphological, thermal, and chemical properties. This hybrid catalyst is specifically engineered for the efficient decomposition of methyl orange (MO) and formaldehyde, demonstrating a significant increase in photocatalytic activity. The TiO2/C/g-C3N4 photocatalyst also exhibits an enhanced specific surface area of 181.2 m2/g, which facilitates increased physical adsorption and photo-catalytic active sites. Experimental results confirm that this catalyst effectively adsorbs MO physically even in the dark without degradation. Combining physical and photo-catalytic functions, this catalyst degrades 94 % of MO within 180 min with the initial concentration 0.2 mol/L of MO, and achieves almost 100 % decolorization of MO under visible light irradiation. Notably, the catalyst retains its high activity after 4 cycles of MO degradation, underscoring its durability and consistent performance. Additionally, the hybrid catalyst features a staggered type-II energy level configuration, which effectively enhances charge separation and boosts photocatalytic efficacy. The incorporation of an ultrafine carbon layer further augments electron mobility towards the surface, crucial for effective catalytic reactions. This study paves the way for future development of highly efficient photocatalytic materials for environmental purification.

Silver vanadate and cerium oxide decorated graphene oxide ternary heterostructure nanocomposites: structural, electrochemical, and optoelectrical properties

In the present work, we synthesized a novel ternary heterostructure nanocomposite comprising Silver Vanadate and Cerium Oxide Decorated Graphene Oxide (AgVO3-CeO2/GO) using a straightforward and cost-effective method. Six samples, including GO, CeO2, CeO2/GO, AgVO3, AgVO3/GO, and CeO2-AgVO3/GO, were prepared. The structural, morphological, electrochemical, and optoelectrical properties of these samples were thoroughly investigated. X-ray diffraction (XRD) demonstrated the presence of graphene oxide, cerium oxide, and silver vanadate phases, while transmission electron microscopy (TEM) showed the single crystalline nature of AgVO3 and the dispersion of CeO2 and AgVO3 nanoparticles within the GO matrix. The heterojunctions between different components facilitated efficient charge transfer and enhanced optoelectronic performance. External quantum efficiency was measured using a 532 nm laser beam, and the electrical properties were evaluated under dark and illuminated conditions with a two-point probe setup. The inclusion of CeO2 and AgVO3 nanoparticles in the GO matrix improved charge transport and interfacial charge transfer processes. These findings highlight the potential of these materials for various optoelectronic applications, including photodetection, sensing, and energy harvesting, with further optimization potentially leading to high-performance devices with enhanced functionality and efficiency.

Unraveling the exceptional kinetics of Zn||organic batteries in hydrated deep eutectic solution

Intuitively, the solvation structure featuring stronger interacted sheath in deep eutectic solution (DES) electrolyte would result in sluggish interfacial charge transfer and intense polarization, which obstructs its practical application in emerging Zn based batteries. Unexpectedly, here we discover a Zn||organic battery with exceptional kinetics properties enabled by a hydrated DES electrolyte, which can render higher discharge capacity, smaller voltage polarization, and faster kinetics of charge transfer in comparison with conventional aqueous 3 M ZnCl2 electrolyte, though its viscosity is two orders of magnitude higher than the latter. The improved kinetics of charge transfer and ion diffusion is demonstrated to originate from the local electron structure regulation of cathode in hydrated DES electrolyte. Furthermore, the DES electrolyte has also been shown to restrict parasitic reaction associated with active water by preferential urea-molecular adsorption on Zn surface and stronger water trapping in solvation structure, giving rise to long-term stable dendrite-free Zn plating/stripping. This work provides a new rationale for understanding electrochemical behaviors of organic cathodes in DES electrolyte, which is conducive to the development of high-performance Zn||organic batteries.

Modulation of pulsed electric field induced oxidative processes in protein solutions by pro- and antioxidants sensed by biochemiluminescence.

Technologies based on pulsed electric field (PEF) are increasingly pervasive in medical and industrial applications. However, the detailed understanding of how PEF acts on biosamples including proteins at the molecular level is missing. There are indications that PEF might act on biomolecules via electrogenerated reactive oxygen species (ROS). However, it is unclear how this action is modulated by the pro- and antioxidants, which are naturally present components of biosamples. This knowledge gap is often due to insufficient sensitivity of the conventionally utilized detection assays. To overcome this limitation, here we employed an endogenous (bio)chemiluminescence sensing platform, which enables sensitive detection of PEF-generated ROS and oxidative processes in proteins, to inspect effects of pro-and antioxidants. Taking bovine serum albumin (BSA) as a model protein, we found that the chemiluminescence signal arising from its solution is greatly enhanced in the presence of as a prooxidant, especially during PEF treatment. In contrast, the chemiluminescence signal decreases in the presence of antioxidant enzymes (catalase, superoxide dismutase), indicating the involvement of both and electrogenerated superoxide anion in oxidation-reporting chemiluminescence signal before, during, and after PEF treatment. We also performed additional biochemical and biophysical assays, which confirmed that BSA underwent structural changes after treatment, with PEF having only a minor effect. We proposed a scheme describing the reactions leading from interfacial charge transfer at the anode by which ROS are generated to the actual photon emission. Results of our work help to elucidate the mechanisms of action of PEF on proteins via electrogenerated reactive oxygen species and open up new avenues for the application of PEF technology. The developed chemiluminescence technique enables label-free, in-situ and non-destructive sensing of interactions between ROS and proteins. The technique may be applied to study oxidative damage of other classes of biomolecules such as lipids, nucleic acids or carbohydrates.

Controllable magnetic anisotropy in two-dimensional 1T-CrTe2 with electrides sublayer

Exploring the controlled magnetic anisotropy energy (MAE) in two-dimensional (2D) ferromagnets is an essential step towards the emergent magnetic tunnel junctions (MTJs) with robust storage stability and low-power consumption. In addition to the transitional charge doping method, we propose that stacking 2D ferromagnet 1T-CrTe2 with electrides substrate can achieve not only the high interfacial charge transfer up to 5.24×1014 cm−2 and but also efficient modification of magnetic behaviors via interfacial engineering. Employing first-principles calculations, we show that the 1T-CrTe2/Ca2N(Y2C) heterostructures exhibit a significant reduction in MAE with a spin reorientation. Notably, the synergistic effect of internal charge transfer, external strain and charge doping shows a significant influence on the magnetic behaviors of the bilayer structures, enabling an efficient modulating of their MAE with distinct dependences. We elucidate that the underlying mechanism is the synergistic effect induced alteration of the spin-polarized px and py states on the Te atom located at the interfaces, which in turn changes the competitive spin-orbit coupling (SOC) contributions to the MAE. These findings provide a practical path toward the controllable MAE in 2D ferromagnets, and make the proposed heterostructures promising candidates for emergent spintronic devices.