Surface Conductivity Research Articles

Cu2ZnSn(S,Se)4 solar cells with over 10% power conversion efficiency enabled by dual passivation strategy

Interfaces quality have always been considered the key factors in the fabrication of efficient Cu2ZnSn(S,Se)4 (CZTSSe) solar cells, and harmful defects at the interface can significantly reduce the performance of the device. Here, we propose a dual passivation strategy by adding Na to the surface of the absorber layer (CZTSSe) to passivate the CZTSSe/CdS interface and treating the buffer layer (CdS) using ultraviolet (UV) irradiation to passivate the CdS/ZnO interface. Due to the Na doping passivation, the absorber surface conductivity increases while the roughness decreases and detrimental defects that can lead to nonradiative recombination are reduced. The power conversion efficiency (PCE) of the cell is improved by about 1 percentage point by Na passivation. The contributions of open-circuit voltage (Voc), short-circuit current density (Jsc), and fill factor (FF) to the improvement of PCE have been quantified as 50.64%, −5.58%, and 54.94%, indicating that Na doping can significantly boost Voc and FF. UV-ozone passivation reduces residual carbon organics in the CdS buffer layer, weakens carrier recombination, allows for more light absorption, and widens the depletion region, which favors efficient carrier collection. The estimated contribution of Voc, Jsc, and FF to the PCE of the device is 8.78%, 119.59%, and −28.37%, respectively, demonstrating that UV-ozone passivation can significantly improve the Jsc of the device. The two passivation strategies complement each other's advantages and achieve a synergistic effect. Our prepared champion device exhibits a PCE of 10.69% and remarkable long-term stability.

Carbamide-mediated facile sol-gel synthesis of porous flower-like ZnCo2O4 microspheres for high-performance asymmetric coin cell supercapacitors

The design and development of ultrahigh-performance nanomaterials possessing novel characteristics are needed to achieve reliable energy storage performance. To satisfy the needs, diverse electrode materials are explored. Even though carbon-based materials hold high surface area and conductivity, their specific capacitance value fails to deliver high-performance applications. Therefore, pseudocapacitive transition metal oxide is adopted to overcome these issues. Among all Zinc Cobaltite, a binary transition metal oxide is widely explored owing to its fascinating electrochemical properties. As most of the synthesis of these kinds of materials requires the hydro/solvothermal method, herein, we have proposed the concept of a facile sol-gel method to prepare this class of materials by using Carbamide as both structure director and fuel to achieve the porous flower-like Zinc Cobaltite. The prepared material delivers the notable gravimetric specific capacitance of 513.3 F g−1. Owing to its unique morphology and porous structure, ion channelization is feasible, which will enhance the electrochemical reaction. Constructed asymmetric coin cell supercapacitor showed an extraordinary specific capacitance of 106.5 F g−1 and energy density of 56.2 Wh kg−1, demonstrating an impressive ability to retain 89.6 % of its capacitance after 4000 cycles at a current density of 6 A g−1. Due to the remarkable electrochemical behavior, this work can act as a guiding tool for designing efficient and cost-effective energy storage devices that will hold prodigious potential in commercial energy storage applications.

Compressed earthen blocks using alluvial clays from Mbam: performance comparison using statistical analysis of cement vs heat-stabilized blocks

AbstractIn the present study, a comparison of the thermal-insulation and mechanical performances of cement and heat-stabilized compressed earthen blocks (CEBs) was carried out to determine the factors which influence those properties. The raw clays used consist mainly of kaolinite, orthoclase and quartz. The mechanical strength increased with increase in both the amount of cement added and the firing temperature. However, the responses are better for cement-stabilized CEBs. The thermal insulation of fired bricks is greater than that of cement-stabilized bricks. This difference was related to the decrease in porosity and the formation of continuous-surface. The decrease in thermal insulation is mainly related to the formation of continuous-surface in cement-stabilized CEBs, whereas in the fired CEBs, it is due to the modification of pore volume. The mineralogy of the raw clays is statistically correlated to porosity and continuous-surface development that were confirmed as the main factors in the modification of both the mechanical strength and the thermal insulation. In cement-stabilization, the decrease in insulation is due to the development of continuous surface, while for heat-stabilization, mineral transformations during the sintering reduced continuous-surface formation and the insulation was controlled by both radiation and reduced surface conduction. The influence of the mineralogy of the raw material shows that clay content favours the insulation in fired bricks obtained at T ≤ 1000°C, while sand contents favour densification. In contrast, clay contents reduce the mechanical response of cement-stabilized material due to limited cement–clay interactions. In general, the mechanical response is more favourable in cement stabilization, while thermal insulation is better in fired bricks.

Production of Stable Electrically Conductive PVDF Membranes Based on Polydopamine-Polyethyleneimine-Assisted Deposition of Carbon Nanotubes.

Electrically conductive membranes (ECMs) have emerged as a multifunctional separation technology that integrates membrane filtration with electrochemical reactions. Physical stability remains a critical challenge for ECMs synthesized by coating polymer membranes with conductive materials. In this article, polydopamine (PDA) and polyethyleneimine (PEI) were used to facilitate the synthesis of significantly more stable ECMs using poly(vinylidene fluoride) (PVDF) ultrafiltration membranes and carbon nanotubes (CNTs). Four different synthesis methods were compared in terms of the final surface stability and separation properties: (1) CNTs deposited on PEI-crosslinked PDA-coated PVDF membranes, (2) PEI-crosslinked CNTs deposited on PDA-coated PVDF, (3) PDA, PEI and CNTs sequentially deposited layer-by-layer on PVDF, and (4) PEI-crosslinked PDA deposited on CNT-coated PVDF. The results revealed that method 1 generated ECMs with the greatest physical stability, highest electrical conductivity (18,518 S/m), and sufficient permeability (395.2 L/(m2·h·bar). In comparison, method 2 resulted in membranes with the highest permeability (2128.5 L/(m2·h·bar), but with low surface conductivity (502 S/m) and poor physical stability (i.e., 53-75% lower peel-off forces compared to other methods). Overall, methods 1, 3, and 4 can be used to make highly conductive membranes with a 97-99% removal of methyl orange by electrochemical degradation at -3 V.

Vacancy and Growth Modulation of Cobalt Hexacyanoferrate by Porous MXene for Zinc Ion Batteries

AbstractPrussian blue analogs (PBAs) featuring with 3D open framework are recognized as promising cathode candidates for Zinc‐ion batteries (ZIBs). However, challenges such as unsatisfactory active site utilization, low conductivity, and abundant structural vacancies have impeded fulfillment of their potential. In this work, a conductive in‐plane porous MXene is for the first time adopted as a multifunctional host material to enhance cobalt hexacyanoferrate (CoHCF) growth and crystallinity. Particularly, the uniform surface charges on MXene are identified to induce anisotropic and highly crystalline CoHCF, which are critical to alleviating the practical drawbacks associated with the PBAs family. Empowered by the targeted modification, the CoHCF nanotube/MXene composite realizes high surface area and low defectiveness, resulting in an impressive capacity of 197 mAh g−1 at 0.1 A g−1 and capacity retention of 95.3% over 3000 cycles at 2.0 A g−1. X‐ray spectroscopy and density functional theory (DFT) reveal that Co─C bonds in the heterostructure facilitate rapid electron/Zn‐ion transfer, enhancing Zn storage kinetics. To validate practical applicability, pouch cells incorporating Zn|CoHCF/MXene are further examined. This composition strategy, utilizing MXene as a multifunctional template, enhances the surface area, conductivity, and crystallinity of PBAs as cathodes for ZIBs, showcasing the significant potential for large‐scale energy storage applications.

Evolution of surface conductivity in SmB6 under nonmagnetic (Yb2+) and magnetic (Eu2+) doping

Among of rare-earth (RE) hexaborides only two compounds SmB6 and YbB6 are discussed in literature to be members of a new class of 3D topological insulators. However, their ground states originate due to different physical mechanisms, including Kondo 4f-5d hybridization and 5d-2p band inversion, respectively. Here we report a comparative study of magnetotransport (resistivity and transverse magnetoresistance) measured on high quality single crystals of YbxSm1-xB6 and EuxSm1-xB6 solid solutions (x ≤ 0.05) at temperatures 1.7 − 300 K in magnetic fields up to 82 kOe. The choice of dopant was determined by the fact that the presence of magnetic/nonmagnetic (Eu2+/Yb2+) impurity in parent SmB6 matrix should lift/not lift the topological protection of surface states. Based on the two-gap paradigm the x-evolution of electron spectra in YbxSm1-xB6 and EuxSm1-xB6 was studied. Our data show that both the 4f lattice coherence (Eg) and the intrinsic gap (Ea) related to many-body states survive under RE doping at least for x ≈ 0.02 − 0.024. We also suggest that the point x(Eu) = 0.05 can be treated as an upper limit of the small gap closing in EuxSm1-xB6 materials. In YbxSm1-xB6 family a negative linear transverse magnetoresistance (TMR) was detected for the first time in the regime of surface conductivity (T < T∗ ≈ 5 K). The TMR anomaly at T∗ caused possibly by the topological protection of surface states in SmB6 is found to survive in Eu-doped compounds but disappears almost completely for Yb-doped compositions in the same fixed magnetic fields. This paradoxical observation is not consistent with general predictions of the topological Kondo insulator (TKI) model.

The mechanism of EP/SiC coating modulated DC flashover characteristics of epoxy composites in SF6/N2 mixtures

Surface flashover is an inevitable insulation issue for basin-type insulators in gas-insulated switchgears/lines, which significantly challenges the reliability of the electrical power systems. Previous studies have indicated that polymer/semiconductor-filler composite coatings effectively improve the insulation properties; however, the influence mechanism of the coating materials on flashover has not been demonstrated from a molecular perspective. In this work, epoxy/silicon-carbide (EP/SiC) composites were coated onto an EP substrate. The energy-level structure, surface trap, surface charging, and DC flashover voltage in SF6/N2 were calculated and characterized, and the process by which the tailored molecular energy level influences surface charge transport and flashover characteristics was elucidated. The incorporating of SiC particles reduced the width of the bandgap and introduced shallow traps, which improved carrier mobility and surface conductivity. Quantitative analysis of charge transport indicated that the improved carrier mobility and reduced surface trap level accelerated the surface charge dissipation. This reduced the tangential electrical field distortion and surface charge density and further impeded gas ionization. When the SiC concentration was 15 wt%, the flashover performance improved by 20.88%. This study describes the mechanism by which the EP/SiC coating regulates the surface charge distribution to improve the surface flashover performance by establishing a relationship among the microscopic molecular energy-level structures, mesoscopic charge transport, and macroscopic discharge phenomena.

Accurate 2-D analytical model for cylindrical gate-junctionless ferroelectric-nanowire (CG-JFe-NW) MOSFET with scaled channel length

In this article, we propose a 2D analytical-model of a cylindrical gate-junctionless ferroelectric-nanowire (CG-JFe-NW) MOSFET for evaluating central potential, electric field, threshold voltage, mobility and current voltage characteristics. Central potential, threshold voltage, and current in the linear and saturation regions are derived by solving the 2D Poisson’s equation employing the parabolic-potential- approximation (PPA) profile. The recommended model is appropriate for compact modelling as it includes the phenomenon of bulk conduction, surface conduction and ferroelectric negative capacitance in all the regions of the device operation. Ferroelectric properties are introduced by combining Silicon doped hafnium oxide (ferroelectric layer) with HfO2 and SiO2 (dielectric layers), and an extensive study has been performed to determine the effects of interfacial-layer thickness and variation of channel length on device performance. For all relevant device characteristics and for all the operational voltage ranges, it is demonstrated that the analytical model entirely corresponds with the numerical simulations. For simulations, the Atlas 3-D simulator has been taken into consideration.

Performance of novolac resin‐ and resole resin‐based carbon/carbon composites in relation to their fabrication conditions

AbstractThe demands of cost‐driven industrial applications can be satisfied by manufacturing composites with a low volume fraction of carbon fibres as phenolic carbon fibre‐reinforced composites and C/C composites, both with acceptable performances, for low‐ or high‐temperature applications, respectively. Polymeric composites reinforced with a low volume fraction (7.5% v/v) of carbon fibres were fabricated using laboratory‐produced phenolic resins, novolac (N) and resole (R), as matrices after different curing/post‐curing temperature profiles. By optimising the manufacturing conditions, the N‐based polymeric composites exhibited higher flexural strength, whereas the R‐based composites showed higher shear strength. C/C composites, namely N‐based and R‐based, were manufactured by pyrolysis of the previously prepared polymeric composites up to 1000 °C. The pyrolysed composites were then densified by impregnation with an appropriate resin solution, followed by curing and new pyrolysis, and particularly by employing 1 up to 4 consecutive cycles of ‘impregnation–curing/pyrolysis’. Weight changes resulting from the impregnation–curing and pyrolysis stages were determined. The curing of both resins was verified by Fourier Transform Infrared Analysis. The apparent density and X‐ray diffraction data of the C/C composites were used to calculate their total percent porosities. The morphology and elemental composition of the C/C composites at their failure region (after flexural testing) were examined by Scanning Electron Microscopy/Energy‐Dispersive X‐ray Analyses. In comparison to the N‐based C/C composites, the R‐based ones exhibited: higher shear strength, lower flexural strength, higher Shore D hardness, slightly higher surface conductivity and lower volume conductivity. The optimum conditions for the manufacture of C/C composites were achieved by applying two consecutive cycles of ‘pyrolysis–impregnation–pyrolysis’ to the polymeric composites. © 2024 The Authors. Polymer International published by John Wiley &amp; Sons Ltd on behalf of Society of Industrial Chemistry.

Capacitive deionization electrode fabrication using activated carbon derived from agriculture by-products toward industry application: A review

Capacitive deionization (CDI), membrane capacitive deionization (MCDI), and flow capacitive deionization (FCDI) are emerging technologies applied to remove ions from brackish water or saline wastewater based on electrode double layer (EDL) mechanisms. The electrode itself can be seen as the most important factor that determines the deionization efficiency of the CDI system. Electrode fabrication using activated carbon derived from agriculture byproducts is a useful solution to decrease cost, restrict environmental pollution, and enable agriculture waste recovery. In this review, the primary parameter's impact on activated carbon (AC) and the electrode fabrication process from the agriculture byproducts is detailed in a discussion to find the most optimal conditions. With excellent characteristics for the activated carbon such as a surface area of up to 2500 m2/g, it can be used to fabricate electrodes that have a high adsorption capacity of approximately 25 mg/g, able to be advanced to 40 mg/g with a modified AC. It can achieve a cycle performance of 95–97 %. The deionization efficiency of the CDI, MCDI, and FCDI systems can be up to 90 % with an input salt concentration from 2000 to 3000 mg/L where the water recovery ratio achieved is 50–90 %, alongside a salt rejection rate of about 7–75 %. AC can be modified to increase its special properties such as surface area, conductivity, and ion selectivity using different methods. The drawbacks and challenges of the CDI technology are also mentioned along with useful solutions such as electrode coating techniques using an anilox roller and a spray, for use in industry applications.

2D zirconium-based metal-organic framework/bismuth(III) oxide nanorods composite for electrocatalytic CO2-to-formate reduction

Electrocatalytic carbon dioxide reduction reaction (eCO2RR) represents one of the most promising technologies for sustainable conversion of CO2 to value-added products. Although metal-organic frameworks (MOFs) can be vastly functionalized to create active sites for CO2RR, low intrinsic electrical conductivity always makes MOFs unfavorable candidates for eCO2RR. Besides, studies on how to regulate eCO2RR activity of MOFs from linkers' functionalities viewpoint lag far behind when compared with the assembly of multinuclear metal-centered clusters. In this work, non-toxic bismuth(III) oxide (Bi2O3) was incorporated into a series of two-dimensional (2D) MOFs (ZrLX) established from Zr-oxo clusters and triazine-centered 3-c linkers with different functionalities (LX = 1–5) to give composites ZrLX/Bi2O3. To investigate how functionalities on linkers distantly tune the eCO2RR performance of MOFs, electron-donating/withdrawing groups were installed at triazine core or benzoate terminals. It is found that ZrL2/Bi2O3 (‒F functionalized on triazine core) exhibits the best eCO2RR performance with the highest Faradaic efficiency (FE) of 96.73% at −1.07 V vs. RHE, the largest electroactive surface (Cdl = 4.23 mF cm−2) and the highest electrical conductivity (5.54 × 10−7 S cm−1), highlighting tuning linker functionalities and hence electronic structure as an alternative way to regulate eCO2RR.

Guiding infrared electromagnetic waves through TI nanowires with extremely large wavenumber and azimuthal index.

In this paper, the dispersion relations of the surface plasmon polaritons (SPPs) in TI nanowires have been investigated. For simplicity, TI nanowire has been modeled as a dielectric cylinder with a conductive surface, the conductivity of which is an anti-symmetric tensor. The off-diagonal terms of the conductivity tensor only slightly change the dispersion relations. Due to small conductivities, these SPPs have extremely large wavenumbers and azimuthal indices; the electric fields are tightly confined near the conductive surface. For high-order modes, cut-off phenomena have been observed. In the end, the effects of losses and much larger bulk permittivities on the dispersion relations of surface plasmons have been discussed. The simple model proposed in this paper can be directly applied to other materials with arbitrary surface conductivity. Our investigations show that TI nanostructures are promising platforms for nanophotonic applications in the future.

Sandwich-type electrochemical immunosensing of CA125 by using nanoribbon-like Ti3C2Tx MXenes and toluidine blue/UIO-66-NH2.

CA125 (carbohydrate antigen 125) is an important biomarker of ovarian cancer, so developing effective method for its detection is of great significance. In the present work, a novel sandwich-like electrochemical immunosensor (STEM) of CA125 was constructed by preparing nanoribbon-like Ti3C2Tx MXenes (Ti3C2TxNR) to immobilize primary antibody (PAb) of CA125 and UIO-66-NH2 MOFs structure to immobilize second antibody (SAb) and electroactive toluidine blue (Tb) probe. In this designed STEM assay, the as-prepared Ti3C2TxNR nanohybrid offers the advantages in large surface area and conductivity as carrier, and UIO-66-NH2 provided an ideal platform to accommodate SAb and a large number of Tb molecules as signal amplifier. In the presence of CA125, the peak currents of Tb from the formed STEM structure increase with the increase of CA125 level. After optimizing the related control conditions, a wide linear range (0.2-150.0 U mL-1) and a very low detection limit (0.05 U mL-1) of CA125 were achieved. It's thus expected the developed STEM strategy has important applications for the detection of CA125.

Nucleation and growth mechanism of Ni/SiC composite coatings electrodeposited with micro- and nano-SiC particles

To study the nucleation and growth mechanism of Ni/SiC composite coatings, electrodeposition was conducted in the Ni bath containing SiC particles with different sizes. Compared to the Ni coating electrodeposited from the bare Ni bath, the Ni/SiC composite coatings exhibited similar grain size but rougher surface morphology due to the incorporation of SiC particles. By means of chronoamperometry (CA) and linear sweep voltammetry (LSV) techniques, it was found that the introduction of SiC particles did not change the nucleation mode of Ni: the Scharifker-Hills three-dimensional instantaneous nucleation mode. However, the nucleation sites on the cathode were reduced due to the inert surface and low conductivity of SiC particles. At a step potential of −0.94 V, Ni presented the maximum nucleation density (N0) of 3.09 × 107 cm−2, which was reduced by one order of magnitude for the Ni/SiC. Furthermore, SiC particles in the bath would extend the diffusion path of Ni2+ ions, resulting in the decrease in diffusion coefficient from 1.04 × 10−7 cm2 s−1 (Ni) to 9.91 × 10−9 cm2 s−1 (Ni/50 nm SiC), 1.83 × 10−8 cm2 s−1 (Ni/500 nm SiC) and 2.29 × 10−8 cm2 s−1 (Ni/5 μm SiC), suggesting the “Blocking effect”. COMSOL simulation further confirmed the “Blocking effect”. The “Blocking effect” would lead to excessive interface gaps around 5 μm SiC particles due to the uneven electrodeposition of Ni. To address the issue, we proposed that adding non-ionic surfactants into the bath to lower the electrochemical reaction rate of Ni2+ ions and accordingly gained composite coatings with fine continuity.

The Effect of Surface Conductivity on the Accumulation and Dissipation of Static Electricity Charges on the Surface of Polymer Dielectrics

The Effect of Surface Conductivity on the Accumulation and Dissipation of Static Electricity Charges on the Surface of Polymer Dielectrics

Surface Resistance Controls Differences in Evapotranspiration Between Croplands and Prairies in U.S. Corn Belt Sites

AbstractWater returned to the atmosphere as evapotranspiration (ET) is approximately 1.6x global river discharge and has wide‐reaching impacts on groundwater and streamflow. In the U.S. Midwest, widespread land conversion from prairie to pasture to cropland has altered spatiotemporal patterns of ET, yet there is not consensus on the direction of change or the mechanisms controlling changes. We measured ET at three locations within the Long‐Term Agroecosystem Research network along a latitudinal gradient with paired rainfed cropland and prairie sites at each location. At the northern locations, the Upper Mississippi River Basin (UMRB) and Kellogg Biological Station (KBS), the cropland has annual ET that is 84 and 29 mm/year (22% and 5%) higher, respectively, caused primarily by higher ET during springtime when fields are fallow. At the southern location, the Central Mississippi River Basin (CMRB), the prairie has 69 mm/year (11%) higher ET, primarily due to a longer growing season. Differences in climate and that the CMRB prairie is remnant native prairie, while the UMRB and KBS prairies are restored, make it challenging to attribute differences to specific mechanisms. To accomplish this, we examine the energy balance using the Two‐Resistance Method (TRM). Results from the TRM demonstrate that higher surface conductance in croplands is the primary factor leading to higher springtime ET from croplands, relative to prairies. Results from this study provide insight into impacts of warm season grasses on the hydrology of the U.S. Corn Belt by providing a mechanistic understanding of how land use change affects the water budget.

Rheological properties of fluorine-free foams stabilized by aluminum hydroxide nanoparticles and mixture of siloxane and hydrocarbon surfactants

Fluorine-free foam stabilized by nanoparticle (NP) is expected to become a new generation of environmental-friendly firefighting foam. Many problems on properties of NP-stabilized fluorine-free foams remain to be studied. The present paper focuses on the rheology and foam stability of fluorine-free foam stabilized by aluminum hydroxide NPs. The surface tension, conductivity, foamability, viscosity, and viscoelasticity of mixed dispersions were measured. The stability, viscosity, viscoelasticity, and thixotropy of foam was analyzed deeply by model fitting and mechanism explanation. The results show that the rheological properties and foam stability of mixed dispersions are both enhanced by the presence of NPs, and the enhancement amplitude increased with NP concentration. Both dispersions and NP-stabilized foams exhibit shear thinning behavior, and the viscosity variations in dispersions conform to the Cross model well. As NP concentration increases, the linear viscoelastic range of foam becomes wider, the flow point of NP foam is delayed, demonstrated enhanced viscoelasticity. The thixotropic recovery of foam decreases with the increasing NP concentration, and foam thixotropic recovery decreases with the increase of irreversible deformation degree. This study can provide design idea for the development of fluorine-free firefighting foam.

Ultrathick MA2N4(M'N) Intercalated Monolayers with Sublayer‐Protected Fermi Surface Conduction States: Interconnect and Metal Contact Applications

AbstractRecent discovery of ultrathick MoSi2N4(MoN)n monolayers open up an exciting platform to engineer two‐dimensional (2D) material properties via intercalation architecture. In this study, a series of ultrathick MA2N4(M'N) monolayers (M, M' = Mo, W; A = Si, Ge) is computationally investigated under both homolayer and heterolayer intercalation architectures, in which the same and different species of transition metal nitride inner core sublayer are intercalated by outer passivating nitride sublayers, respectively. The MA2N4(M'N) are stable metallic monolayers with excellent mechanical strength. Intriguingly, the metallic states around Fermi level are localized within the inner core sublayer. Carrier conduction mediated by electronic states around the Fermi level is thus spatially insulated from the external environment by the native outer nitride sublayers, suggesting the potential of MA2N4(M'N) in back‐end‐of‐line metal interconnect applications. N and Si (or Ge) vacancy defects at the outer sublayers create ‘punch through’ states around the Fermi level that bridges the carrier conduction in the inner core sublayer and the outer environment, forming an electrical contact akin to the ‘via' structures of metal interconnects. It is further shown that MoSi2N4(MoN) can serve as a quasi‐Ohmic contact to 2D WSe2. These findings reveal the potential of ultrathick MA2N4(MN) monolayers in interconnect and metal contact applications.

Spin-splitting and spin Hall effect of reflected Airy beams on the surface of topological insulator

We present an analysis of the enhanced spin Hall effect of light (SHEL) resulting from a reflected Airy beam off the interface of an air-topological insulator (TI). Our study suggests that the surface conductivity of TI film and the decay factors of Airy beams are crucial in increasing the spin-splitting distance and the spatial shifts of the left-handed circularly polarized (LCP) and right-handed circularly polarized (RCP) components. An apparent spatial shift asymmetry depending on the decay factors can be observed between the LCP and RCP components, where the coupling of intrinsic and extrinsic angular momentum will play a significant impact. The connection among the thickness of TI film, chemical potential and the incident frequency at the fixed decay factors is thoroughly examined to achieve the maximum of spatial shifts. We find that the coupling between the upper and lower surfaces’ conductivity could be responsible for the pronounced SHEL. These conclusions can be extended to other interfaces of comparable structures, such as insulators coated with a layer of two-dimensional Dirac material. Our work provides novel insights into the use of innovative beams incident on the surface of TI film and their potential applications in optical detection.

Sandwich-Like Electrochemical Immunosensing of Squamous Cell Carcinoma Antigen Based on Gold Nanoparticles/Reduced Graphene and Toluidine Blue/UIO-66-NH2

Squamous cell carcinoma antigen (SCCA) is an important biomarker in the diagnose of cancer, so developing effective methods for its detection is of great significance. In the present work, a novel sandwich-like electrochemical immunosensing assay (STEM) of SCCA was constructed by preparing gold nanoparticle/reduced graphene-oxide (Au NPs/rGO) to immobilize primary antibody (PAb) of SCCA and UIO-66-NH2 MOFs structure to immobilize second antibody (SAb) and electroactive toluidine blue (Tb) probe. In this designed STEM assay, the prepared Au NPs/rGO nanohybrid offers the advantages in large surface area and conductivity as carrier, and UIO-66-NH2 provided an ideal platform to accommodate SAb and a large number of Tb molecules as signal amplifier. In the existence of SCCA, the current peaks of Tb from the formed STEM structure increase with the increase of SCCA level. After optimizing the related control factors, a wide linear range (0.01 pg ml−1 and 15.0 ng ml−1) and very low detection limit (0.003 pg ml−1) of SCCA was achieved, it’s thus expected the designed STEM strategy has important applications for the detection of SCCA.