Kelvin Probe Force Microscopy Research Articles

Highly Tunable Moiré Superlattice Potentials in Twisted Hexagonal Boron Nitrides.

Moiré superlattice of twisted hexagonal boron nitride (hBN) has emerged as an advanced atomically thin van der Waals interfacial ferroelectricity platform. Nanoscale periodic ferroelectric moiré potentials in twisted hBN allow the hosting of remote Coulomb superlattice potentials to adjacent 2D materials. Therefore, the new strategies for engineering moiré length, angle, and potential strength are essential for developing programmable quantum materials. Here, it demonstrates the realization of twisted hBN-based moiré superlattice platforms and visualizes the moiré domains and ferroelectric properties using Kelvin probe force microscopy (KPFM). Also, the regular moiré superlattice in the large area is reported. It offers the possibility to reproduce uniform moiré structures with precise control piezo stage stacking and heat annealing. It demonstrates cumulative multi-ferroelectric polarization and multi-level domains with multiple angle mismatched interfaces. Additionally, it observes the quasi-1D anisotropic moiré domains and show the highest resolution analysis of the local built-in strain between adjacent hBN layers compared to the conventional methods. Furthermore, in-situ manipulation of moiré potential is demonstrated using femtosecond pulse laser, which results in the optical phonon-induced atomic displacement at the hBN moiré interfaces. The results pave the way to develop precisely programmable moiré superlattice platforms and investigate strongly correlated physics.

Non-Destructive Integration of Spark-Discharge Produced Gold Nanoparticles onto Laser-Scribed Graphene Electrodes for Advanced Electrochemical Sensing Applications

Gold nanoparticles (AuNPs) decorated graphene materials are preferable materials in a wide range of electrochemical applications, however, the current methods for preparing them have several limitations. Herein, we have developed a green, solution-free, and non-destructive method for the in-situ generation of AuNPs on laser-scribed graphene electrodes (LSGEs), addressing the limitations of traditional preparation methods. This novel technique, contrasting with the conventional solution-based electrochemical deposition, utilizes spark discharge to modify LSGEs, demonstrating superior performance in sensors and biosensors applications. Through comprehensive characterizations (scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), Raman spectra, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Kelvin probe force microscopy (KPFM)), we observed significant distinctions in particle size, metal loading, stability, surface-to-volume ratio, and graphene quality between spark-discharge produced AuNPs (SP-AuNPs) and electrodeposition produced AuNPs (EC-AuNPs). The average particle sizes of the SP-AuNPs and EC-AuNPs are 10 nm and 38 nm, respectively. The SP-AuNPs modified LSGEs demonstrate exceptional electroanalytical performance in dopamine detection, with a broad detection range (0.6–90 µM) and low LOD (0.40 µM), further validated in human neuroblastoma cells SH-SY5Y. Our findings suggest that the spark discharge method represents a significant advancement in the synthesis of metal nanoparticle enhanced LSG electrodes, with broad implications for electrochemical sensing, biosensing, and biomedical applications.

Real-space investigation of polarons in hematite Fe2O3.

In polarizable materials, electronic charge carriers interact with the surrounding ions, leading to quasiparticle behavior. The resulting polarons play a central role in many materials properties including electrical transport, interaction with light, surface reactivity, and magnetoresistance, and polarons are typically investigated indirectly through these macroscopic characteristics. Here, noncontact atomic force microscopy (nc-AFM) is used to directly image polarons in Fe2O3 at the single quasiparticle limit. A combination of Kelvin probe force microscopy (KPFM) and kinetic Monte Carlo (KMC) simulations shows that the mobility of electron polarons can be markedly increased by Ti doping. Density functional theory (DFT) calculations indicate that a transition from polaronic to metastable free-carrier states can play a key role in migration of electron polarons. In contrast, hole polarons are significantly less mobile, and their hopping is hampered further by trapping centers.

Fermi level regulation of single-walled carbon nanotubes by metal chloride doping for enhanced NO2 sensing performance

Pristine single-walled carbon nanotubes (SWCNTs) typically exhibit limited sensitivity due to the low charge transfer dynamics between nanotubes and gas molecules. Among various enhancement methods, the Fermi level regulation proves to be effective in promoting the charge transfer between SWCNTs and gas molecules, consequently improving the sensing performance. Herein, we firstly report a non-destructive method to regulate the Fermi level of SWCNTs through doping metal chlorides, and the interfacial charge transfer between SWCNTs and different metal chlorides has been well investigated by combining Raman shift with X-ray photoelectron spectroscopy. Experimental results reveal that the interfacial charge transfer dynamics determine the sensing properties of SWCNTs doped with chlorides. The as-fabricated FeCl3-doped SWCNT sensors exhibit a high response of 196.9 % in response to 100 ppb NO2 gas with excellent selectivity. The Kelvin probe force microscope (KPFM) results directly prove the doping effect of metal chlorides due to the shift down of Fermi level of SWCNTs after doping FeCl3. Our work not only proposes a novel method to controllably regulate the Fermi level of SWCNTs but also provides a guidance for high-performance SWCNT-based sensing devices.

Probing Nanoscale Charge Transport Mechanisms in Quasi-2D Halide Perovskites for Photovoltaic Applications.

Quasi-2D layered halide perovskites (quasi-2DLPs) have emerged as promising materials for photovoltaic (PV) applications owing to their advantageous bandgap for absorbing visible light and the improved stability they enable. Their charge transport mechanism is heavily influenced by the grain orientation of their crystals as well as their nanostructures, such as grain boundaries (GBs) and edge states─the formation of which is inevitable in polycrystalline quasi-2DLP thin films. Despite their importance, the impact of these features on charge transport remains unexplored. In this study, we conduct a detailed investigation on polycrystalline quasi-2DLP thin films and devices, carefully analyzing how grain orientation and nanostructures influence charge transport. Employing nondestructive atomic force microscopy (AFM) topography, along with transient absorption spectroscopy (TAS) and grazing-incidence wide-angle X-ray scattering (GIWAXS), we obtained significant insights regarding the phase purity, crystallographic information, and morphologies of these films. Moreover, our systematic investigation using AFM-based techniques, including Kelvin probe force microscopy (KPFM) and conductive AFM (c-AFM), elucidates the roles played by GBs and edge states in shaping charge transport behavior. In particular, the local band structure along the GBs and edge states within both vertical and parallel grains was found to selectively repel electrons and holes, thus facilitating charge carrier separation. These findings provide perspectives for the development of high-performance quasi-2DLP PV devices and highlight potential approaches that can leverage the intrinsic properties of quasi-2DLPs to advance the performance of perovskite solar cells.

Organic Bulk-Heterojunction Blends with Vertical Phase Separation for Enhanced Organic Photodetector Performance.

The ternary blending strategy is a fundamental approach that is widely recognized in the field of organic optoelectronics. In our investigation, leveraging the inherent advantages of the ternary component blending methodology, we introduced an innovative design for organic photodetectors (OPDs) aimed at reducing the dark current density (Jd) under reverse bias. This pioneering effort involved combining two distinct conjugated molecules (IT-4F and IEICO-4F) with a conjugated polymer (PM7), resulting in a composite material characterized by a well-defined vertical phase separation. To thoroughly explore device performance variations, we utilized a comprehensive array of analytical techniques, including atomic force microscopy (AFM) cross-section methodologies and Kelvin probe force microscopy (KPFM). Through the optimization of the blend ratio (PM7:IT-4F: IEICO-4F at 1:0.8:0.2), we achieved significant advancements. The resulting OPD demonstrated an exceptional reduction in JD, reaching a remarkably low value of 4.95 × 10-10 A cm-2, coupled with an ultra-high detectivity of 4.95 × 1013 Jones and an outstanding linear dynamic range exceeding 100 dB at 780 nm under a bias of -1V. Furthermore, the attained cutoff frequency reached an impressive 220 kHz, highlighting substantial improvements in device performance metrics. Of particular significance is the successful translation of this technological breakthrough into real-world applications, such as in heart rate sensing, underscoring its tangible utility and expanding its potential across various fields. This demonstrates its practical relevance and underscores its versatility in diverse settings.

Porphyrinoid-Functionalized ZnO Nanoflowers for Visible Light-Enhanced and Selective Benzylamine Detection at Room Temperature.

Functionalization of hybrid organic molecules as layers on ZnO nanoflowers (NFs) gives an excellent combination of sensing toward visible light and vapors of various volatile organic compounds (VOCs). In this work, hybrid organic molecules functionalized ZnO NFs were utilized for the photoinduced detection of benzylamine at room temperature. The ZnO NFs were synthesized via a facile solution route and functionalized with four different porphyrin-conjugated molecules namely (i) pyrene-porphyrin (PP), (ii) pyrene- porphyrinato zinc (ZnPP), (iii) triphenylamine- porphyrin (TP) and (iv) triphenylamine- porphyrinato zinc (ZnTP). The diameter of the flower-like structure was found to be ∼3.2 μm with the thickness of petals being ∼24.1 nm. The gas adsorption performance of the functionalized ZnO NFs on light activation at room temperature was studied by using a scanning Kelvin probe (SKP) system. The improved adsorption properties of the samples can be attributed to the heterojunctions and light activation. In particular, an enhanced response of ZnTP functionalized ZnO (ZnTPZ) toward benzylamine was observed. Further, static gas sensing experiments using ZnTPZ under various concentrations (1, 3, 5, 10, 15, and 25 ppm) of benzylamine vapors both in dark and visible light conditions have exhibited a linear increase in the response. The selectively enhanced response of ZnTPZ compared to that of pristine ZnO was thus confirmed at 1 ppm of benzylamine. The sensitivity and limit of detection of the ZnTPZ sensor were calculated to be 0.0292 ppm-1 and 197 ppb, respectively. The coordination metal (Zn) has helped in effective charge transfer between benzylamine and ZnTPZ by providing additional active sites for interactions. Also, density functional theory calculations demonstrated the role of the hybrid organic molecules on the sensor surface in improving gas adsorption. Further, fresh cabbage was utilized for real sample analysis with the proposed sensor under visible light illumination conditions, and a linear response was obtained for low ppm evaluation at room temperature. Overall, the obtained results suggest the development of novel ZnTPZ-based light-activated gas sensors for low ppm benzylamine detection at room temperature. These kinds of sensors can be used to track the freshness of vegetables as they are transported from farms to commercial outlets.

Electrochemical production of ammonia: Nitrate reduction over novel Cu-Ni-Al metallic glass nanoparticles used as highly active and durable catalyst

It is a great challenge to design and synthesize catalysts that can regulate both adsorption and desorption processes for electrocatalytic nitrate reduction to ammonia (NRA). Herein, amorphous Cu-Ni-Al nanometallic glasses (NG) were synthesized using a facile thermal evaporation coupled Joule heating method. The Cu50Ni25Al25-NG exhibits remarkable Faradaic efficiency (98.81 %) and NH3 yield-rate (211.14 μmol h−1cm−2) at an outstanding positive potential of −0.15 V vs. RHE. Aluminum atoms of low work-function when intercalated at different positions in Cu50Ni25Al25-NG enhance both adsorption and desorption processes during NRA. The oscillatory properties of surface potential detected by Kelvin-probe force microscopy demonstrate the diversity of active sites on Cu50Ni25Al25-NG. Two potential-regulated reaction mechanisms in NRA on the surface of Cu50Ni25Al25-NG were proposed using in-situ electrochemical Raman spectra. This work provides a new method for the preparation of multi-element NG enriched with low work-function metals and a new idea for the synthesis of synergistic catalytic-sites for NRAs.

Gas sensing properties of Ti0.2V1.8CTx/V2O5 nanocomposite

A method for the preparation of nanocomposite containing Ti0.2V1.8CTx MXene core and titanium-doped vanadium oxide surface layers as a result of relatively low-temperature partial oxidation of MXene multilayer - two-dimensional vanadium-titanium carbide has been developed. It is shown that during oxidation in air atmosphere of initial Ti0.2V1.8CTx at temperature 250°С, in general, the microstructure of accordion-like aggregates with some increase in porosity of their constituent layers and increase in their thickness due to the formation of V2O5 is preserved. At the same time, preservation of the MXene structure with a decrease in the interplanar spacing from 10.3 (initial powder Ti0.2V1.8CTx) to 7.3 Å was observed. Raman spectroscopy confirmed the formation of vanadium oxide. Kelvin-probe force microscopy data revealed that the formation of Ti0.2V1.8CTx/V2O5 nanocomposite results in a decrease in the work function from 4.88 (Ti0.2V1.8CTx) to 4.68 eV. The chemosensor properties towards a range of gaseous analytes (H2, CO, NH3, NO2, C6H6, C3H6O, CH4, C2H5OH and O2) have been comprehensively studied for Ti0.2V1.8CTx/V2O5 layers coated using the microplotter printing. At increased detection temperatures (125–200°С), high sensitivity to oxygen (10% O2) and NO2 (100 ppm) is observed; there are notable responses to humidity (50% RH) throughout the 25–200°С temperature range. At room temperature, good response to acetone, ethanol and ammonia is observed.

Interface and Defect Engineering in 3D Co3O4‐Ov/TiO2 to Boost Simultaneous Removal of BPA and Cr(VI) upon Photoelectrocatalytic/Peroxymonosulfate (PEC/PMS) System

AbstractThe combination of photoelectrocatalytic (PEC) and peroxymonosulfate (PMS) is an innovative strategy for environmental treatment. And fabricating a highly efficient photoelectrode is the most pivotal factor in PEC reactions. This study designs an advanced Co3O4‐Ov/TiO2 photoelectrode by a dual‐modification strategy encompassing interface engineering and defect engineering. The photoelectric characterization validates the synergy of oxygen vacancies and dual heterojunctions. Simulated electron density distribution and Kelvin probe force microscopy (KPFM) elucidate the charge transfer pathway between Co3O4‐Ov and TiO2. 1O2 and SO4 .− are confirmed to be primarily responsible for the BPA oxidation in PEC/PMS system by radical scavenger experiments and the EPR technique. And the attack sites of BPA are precisely identified based on the Fukui index. Furthermore, density functional theory (DFT) calculations testify that Co3O4‐Ov can improve the adsorption capacity of PMS and reduce the energy barrier of the reaction process, while XPS analysis showed Co3+/Co2+ redox couple can accelerate PMS activation. Enhanced anode oxidation can effectively promote cathode reduction and consequently Co3O4‐Ov/TiO2‐PMS/PEC system presents a superior removal of both pollutants within only 15 min with fast kinetics (0.15 min−1 for BPA, 0.29 min−1 for Cr(VI)). This work provides unique insight into designing a highly efficient PMS/PEC system for simultaneous pollutant treatment.

Robust photocatalytic hydrogen evolution performance of 0D/1D NiO/CdS S-scheme heterojunction

Constructing heterojunction, especially S-scheme heterojunction, is an effective strategy for achieving effective separation of photogenerated electron-hole pairs and obtaining high electrode potential. In this study, a unique 0D/1D NiO/CdS S-scheme heterojunction was constructed by solvent evaporation induced self-assembly method. The loading of NiO was found to greatly enhance the photogenerated carrier separation efficiency of CdS by photoluminescence (PL) spectroscopy, electrochemical impedance spectroscopy (EIS), Kelvin probe force microscopy (KPFM) and transient photocurrent tests. The best photogenerated carrier separation effect was observed at a NiO loading ratio of 15 wt% and the largest photocatalytic hydrogen evolution rate reached 7.89 mmol h-1g−1 under visible light, which was 24.66 times that of pristine CdS. In addition, the cycling experiments showed that the loading of NiO led to the alleviation of the photocorrosion phenomenon of CdS, and the performance remained at 94.2 % after five cycles. This is due to the fact that the formation of S-type heterojunction combines the photogenerated holes of CdS with the photogenerated electrons of NiO, which hinders the oxidation of S2- on the surface of CdS, thus alleviating the photocorrosion phenomenon of CdS and improving the stability of CdS. This work furnishes a new strategy for the development of stable and high-performance photocatalysts with inexpensive co-catalysts.

Citric acid modulated strong magnetic CoFe-LDH/CoFe2O4 coupled dielectric barrier discharge plasma for efficient levofloxacin degradation: Enhanced internal electric field and accelerated electron migration

A novel citric acid (CA) modulation strategy was developed to prepare strong magnetic CoFe-LDH/CoFe2O4-C composites, which were combined with dielectric barrier discharge (DBD) to effectively degrade levofloxacin (LEV) in wastewater. Kelvin probe force microscopy (KPFM) test showed that CA modulation facilitated a more powerful internal electric field to drive rapid charge migration. The addition of CoFe-LDH/CoFe2O4-C increased LEV degradation from 78.2% to 98.6% and reduced energy efficiency from 24.77 to 8.93 kWh m–3. Quenching experiments and electron paramagnetic resonance (EPR) spectra showed the CoFe-LDH/CoFe2O4-C could take full advantage of the active substances originating from DBD plasma and highlighted the role of 1O2 and ·O2–. Density functional theory (DFT) calculation revealed that the heterojunction can not only drive faster electron migration but also reduce the energy barrier of O3 decomposition. Possible degradation pathways for LEV were proposed. This study opened up a new avenue for the synthesis of applicable catalysts for plasma systems in water treatment areas.

Dual electric field and defect engineering induced multi-channel electron transfer for boosting photocatalytic hydrogen production on Cu2+-doped ZnMoO4/ZnIn2S4 heterojunction

Serious recombination of photogenerated carriers is the bottleneck problem of achieving high-performance photocatalytic reaction. A high efficient Cu2+-doped ZnMoO4/ZnIn2S4 (CZMOZIS) heterojunction was synthesized by hydrothermal method. The CZMOZIS heterostructure achieved hydrogen production of 11637.5 µmol g−1 within 5 h, which was 9.7 times higher than that of pure ZnIn2S4. Comprehensive characterization and theoretical calculation demonstrated that the CZMOZIS composites exhibited broad light absorption, an increased specific surface area and an optimized Gibbs free energy. The presence of oxygen vacancies in CZMOZIS composites was confirmed by X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy, revealing the formation of defect levels below the conduction band (CB) of ZnMoO4. Kelvin probe force microscopy (KPFM) and Zeta potential demonstrated that the intrinsic electric field (IEF) of the CZMOZIS heterojunction was enhanced, which may be attributed to the generation of polarization electric field (PEF). The double electric field provided a robust driving force for the photogenerated carrier migration and separation. The electrons in the CB and defect levels of Cu2+-ZnMoO4 could be coupled with the holes of ZnIn2S4, thereby forming a multi-channel electron transfer. This work provides a theoretical support for promoting charge transfer to improve photocatalytic performance by dual electric field and defect engineering.

Thermal Plasma‐Induced Surface Modifications Correlated With the Field Emission Properties of Copper

ABSTRACTThe present work deals with the Argon (Ar) Thermal plasma‐induced surface modification of Cu and its correlation with the electrical and field emission (FE) properties. Polycrystalline Cu targets were treated with Ar thermal plasma under atmospheric pressure at different treatment times ranging from 5 min to 30 min. XRD patterns revealed the absence of new phase in treated samples. However, significant variation in peak intensities and shifting is observed, which is explained on the basis of thermal plasma ions induced defect generation and annihilation processes. The electrical conductivity of processed Cu targets measured by four‐probe method ranges from 1.9 MS/m to 70 MS/m and is well correlated with the crystallite size variation. Surface modification induced work function alternations investigated by employing Scanning Kelvin Probe (SKP) technique are in the range of 4.69 eV 4.97 eV. The irradiated morphology explored by optical and scanning electron microscopy analyses revealed the formation of localized melt pools, grains, hillocks, spheroids, and sputtered patches, which are explainable on the basis of Coulomb's explosion, thermal spike model, plasma‐induced sputtering, and re‐deposition. FE properties of thermal plasma‐treated Cu are measured in diode configuration by measuring I‐V characteristics of target under ultra‐high vacuum condition. The improved FE parameters such as turn‐on field (Eo), field enhancement factor (β), and maximum current density (Jmax) come out to be in the range of 3–7.5 V/μm, 1715–3223, and 284–872 nA/cm2, respectively and their correlation with plasma‐induced surface structural, morphological and work function modifications is discussed.

Amorphous-Crystalline Interface Induced Internal Electric Fields for Electrochromic Smart Window.

Balancing optical modulation and response time is crucial for achieving high coloration efficiency in electrochromic materials. Here, internal electric fields are introduced to titanium dioxide nanosheets by constructing abundant amorphous-crystalline interfaces, ensuring large optical modulation while reducing response time and therefore improving coloration efficiency. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) reveals the presence of numerous amorphous-crystalline phase boundaries in titanium dioxide nanosheets. Kelvin probe force microscopy (KPFM) exhibits an intense surface potential distribution, demonstrating the presence of internal electric fields. Density functional theory (DFT) calculations confirm that the amorphous-crystalline heterointerfaces can generate internal electric fields and reduce diffusion barriers of lithium ions. As a result, the amorphous-crystalline titanium dioxide nanosheets exhibit better coloration efficiency (35.1cm2C-1) than pure amorphous and crystalline titanium dioxide nanosheets.

Beta-cyclodextrin supported Bi2Fe4O9-based n-p/n hetero-homojunction: A leach proof S-scheme photocatalyst for mitigation of micropollutants

The work proffers a novel Bi2Fe4O9 based n-p/n hetero-homojunction that offers excellent photocatalytic activity towards mitigation of three potential pharmaceutical and agrochemical pollutants. Nanoparticles of Prunus Amygdalus Dulcis shell derived carboxyl functionalized reduced graphene oxide (rGO) were encrusted over the surface of hydrothermally fabricated Bi2Fe4O9 nanoplates. Further, hydroxyl functionalization of fabricated composites was performed using beta-cyclodextrin (β-CD) and the fabricated materials were utilized for oxidative degradation of doxorubicin, levofloxacin drugs and malathion pesticide. The proffered modification not only enhanced the catalytic activity but also protected the surface of Bi2Fe4O9, which resulted 89.06 % and 86.84 % suppression in leaching of Fe and Bi ions as that of pristine bismuth ferrite (BF) was achieved with this beneficial modification. Practical viability of fabricated hetero-homojunction was testified via treating real pharmaceutical wastewater at lower concentration. Mott-Schottky (MS), Diffuse reflectance spectroscopy (DRS) and Kelvin Probe Force Microscopy (KPFM) studies were employed to investigate the band structure and charge transfer mechanism of fabricated n-p/n hetero-homojunction.

Electrical Response of Different Crystalline Microregions in Poly(vinylidene fluoride).

The crystal structure has a great influence on the dielectric and piezoelectric performance of poly(vinylidene fluoride) (PVDF). In this work, we prepared PVDF films with two typical crystalline phases (α and β). In situ Kelvin probe force microscopy (KPFM) and Piezoelectric force microscopy (PFM) were employed to investigate the responses of different PVDF crystalline phases to charge mobility, polarization, and piezoelectric properties. We used a homemade Kelvin probe force microscope (KPFM) to inject charges into the two crystalline phases to investigate the differences in the response of different crystalline phases of PVDF to electrical excitation on a microscopic scale. It was found that the α-phase has a lower charge injection barrier and is more susceptible to charge injection and that the α-phase is accompanied by a faster charge dissipation rate, which makes it easier to accumulate charge at the interface between the α-phase and β-phase PVDF. Moreover, the PFM polarization manipulation showed no change in the amplitude and phase diagram of the α-phase under ±10 V bias. In contrast, the β-phase showed a clear polarization reversal phenomenon and a significant increase in piezoelectric amplitude, which is consistent with its polar intrinsic properties. This study provides valuable insights into the multiphase contributions and a reference for designing advanced PVDF dielectrics.

Optoelectronic properties of chemical vapor deposition grown monolayer MoS2 nanowires

Monolayer (1 L) MoS2 nanowire possesses large amount of exposed edges, resulting in unique physical properties differing to the large size flake. Preparation of high quality 1 L MoS2 nanowire using chemical vapor deposition (CVD) is still challenging to the best of our knowledge. Herein, by employing space-confined CVD method using Mo foil as Mo source, 1 L MoS2 nanowires with width of ∼70 nm can be deposited on the surface of 1 L MoS2 flake. Tip-enhanced photoluminescence (TEPL) measurements indicate different PL peak position and intensity distribution across the nanowires. Photosensitive Kelvin probe force microscopy (KPFM) measurements further reveal that these nanowires exhibit lower Fermi level than the 1 L MoS2 flake, resulting in tunable optosensitive charge transfer under different excitation photon energies form 1.58 eV to 2.33 eV.

Investigation of Persistent Photoconductivity of Gallium Nitride Semiconductor and Differentiation of Primary Neural Stem Cells.

A gallium nitride (GaN) semiconductor is one of the most promising materials integrated into biomedical devices to play the roles of connecting, monitoring, and manipulating the activity of biological components, due to its excellent photoelectric properties, chemical stability, and biocompatibility. In this work, it was found that the photogenerated free charge carriers of the GaN substrate, as an exogenous stimulus, served to promote neural stem cells (NSCs) to differentiate into neurons. This was observed through the systematic investigation of the effect of the persistent photoconductivity (PPC) of GaN on the differentiation of primary NSCs from the embryonic rat cerebral cortex. NSCs were directly cultured on the GaN surface with and without ultraviolet (UV) irradiation, with a control sample consisting of tissue culture polystyrene (TCPS) in the presence of fetal bovine serum (FBS) medium. Through optical microscopy, the morphology showed a greater number of neurons with the branching structures of axons and dendrites on GaN with UV irradiation. The immunocytochemical results demonstrated that GaN with UV irradiation could promote the NSCs to differentiate into neurons. Western blot analysis showed that GaN with UV irradiation significantly upregulated the expression of two neuron-related markers, βIII-tubulin (Tuj-1) and microtubule-associated protein 2 (MAP-2), suggesting that neurite formation and the proliferation of NSCs during differentiation were enhanced by GaN with UV irradiation. Finally, the results of the Kelvin probe force microscope (KPFM) experiments showed that the NSCs cultured on GaN with UV irradiation displayed about 50 mV higher potential than those cultured on GaN without irradiation. The increase in cell membrane potential may have been due to the larger number of photogenerated free charges on the GaN surface with UV irradiation. These results could benefit topical research and the application of GaN as a biomedical material integrated into neural interface systems or other bioelectronic devices.

Corrosion behavior of 70/30 cupronickel in electrolytic seawater antifouling environment

Available chlorine is most commonly used in seawater cooling systems to eliminate biofouling. The corrosion behavior of 70/30 cupronickel alloy after exposure to seawater with different concentrations of available chlorine was studied by electrochemical and immersion tests. The electrochemical measurements show that 100 ppm available chlorine accelerates the corrosion of 70/30 cupronickel alloy in seawater. The corrosion rate of 70/30 cupronickel sample in seawater with 100 ppm available chlorine is 3–4 times higher than that in seawater with 0–10 ppm available chlorine. Scanning Kelvin probe (SKP) and scanning vibrating electrode technique (SVET) results demonstrate that the local electrochemical reaction of 70/30 cupronickel alloy is more active after soaking in seawater with 100 ppm available chlorine. Energy dispersive spectroscopy (EDS) results reveal that Cl element in the corrosion products is enriched after exposure to seawater with 100 ppm available chlorine. X-ray photoelectron spectroscopy (XPS) analysis demonstrates that the corrosion product of 70/30 cupronickel sample contains more Cu2(OH)3Cl after being immersed in seawater with 100 ppm available chlorine.