Spin Polarization Research Articles

Dwell time and spin polarization for electron in single ferromagnetic-stripe device modulated by spin–orbit couplings

Considering both Zeeman effect and spin–orbit coupling, we calculate dwell time for electron in single ferromagnetic-stripe device (SFSD), which can be constructed by patterning a nanosized ferromagnetic stripe on the surface of GaAs/AlxGa1-xAs heterostructure. Due to an intrinsic symmetry in the SFSD, dwell time is independent of electron spins, if only Zeeman effect is involved. However, the intrinsic symmetry is broken by spin–orbit coupling, which gives rise to spin-dependent dwell time for electron in the SFSD. As a result, electron spins can be separated in time dimension, which induces an obvious electron-spin polarization effect in the SFSD. Spin polarization ratio can be efficaciously modified by interfacial confining electric-field or strain engineering, which attributes to the dependence of effective potential felt by electron in the SFSD on spin–orbit couplings. Thus, the SFSD can act as a controllable temporal electron-spin splitter, a class of electron-spin polarized sources in semiconductor spintronics.

Modulating photocatalytic activity of nitrogen doped TiO2 nanoparticles via magnetic field

The effect of the magnetic field on the photocatalytic activity of TiO2-based nanoparticles is analyzed using a magnetically-assisted photoreactor with permanent magnets to generate a controlled uniform magnetic field, B (≈ 82 mT). Nitrogen doped TiO2 nanoparticles (sizes around 10 nm) were synthesized through a solvothermal method employing Ti(IV) butoxide and HNO3 (x = 0, 0.5, 1, 1.5 and 2 mL) as precursors and their structural, optical and magnetic properties were analyzed. Specifically, nitrogen doping is confirmed through Hard X-ray Photoelectron Spectroscopy (HAXPES) in those samples synthesized with low HNO3 concentrations (x = 0.5, 1). The correlation between spin polarization (magnetic susceptibility) and visible photocatalytic activity (methyl orange as a model organic pollutant) is particularly analyzed. Surprisingly, opposite effects of the magnetic field on the photocatalytic performance are found in the visible range (above 400 nm) or under UV-Vis irradiation (decrease and increase in the photocatalytic activity, respectively, under magnetic field). The Langmuir-Hinshelwood model allows us to conclude that the strong decrease in adsorption under the magnetic field (around 42 % for x = 0.5) masks the increase in the kinetic constant (close to 58 % for x = 0.5) related mainly to the effect of Lorentz forces on the reduction of the electron-hole recombination.

Quenching controlled spin exchange interactions and spin selective electron transfer for oxygen evolution reactions

The utilization of magnetic field to enhance electrocatalytic activity has become an effective strategy garnering significant attention in the field of electrocatalysis. Herein, we employ a combination of electrospinning and quenching techniques to successfully synthesize high-entropy oxide (HEO) (FeCoNiCrMn)3O4. The HEO exhibited ferromagnetic properties and further increased the saturation magnetization after the quenching process, primarily due to temperature-mediated magnetic exchange interactions. The OER performance is significantly improved by employing a ferromagnetic ordered catalyst as a spin polarizer in the presence of a magnetic field. The introduction of an exterior magnetic field (∼130 mT) significantly improved the OER performance of HEO-LN (HEO quenching in liquid nitrogen), reducing the overpotential by 39.4 mV at 10 mA cm-2. The improved OER performance is due to the presence of the magnetic field-enhanced electron spin polarization, reducing electron repulsion and enhancing orbital hybridization. These findings not only provide crucial insights into understanding reactions involving magnetic field-induced electrochemistry but also contribute to the rational design of electrocatalysts with magnetic effect.

Employing lattice compression spin polarization electric field for boosting degradation of mixed antibiotics in wastewater

Localized polarization electric field is a key factor affecting photocatalytic activity. In this study, the localized polarization electric field of lattice strain was introduced into the electronic structure of Bi2WO6 by using the high and low valence state doping method. The impurity energy level induced by lattice strain further affects the gap energy level. As an intermediate state for electron transfer, the gap level further promotes the dynamics of photo generated charges, reducing the band gap by 0.4 eV and improving the photoelectric performance by 60 %. Various tests and theoretical calculations have confirmed that the internal electric field of local polarization significantly improves the generation and transfer rate of photo-generated charges, thereby boosting catalytic activity. The removal ratios of ciprofloxacin (CIP) and tetracycline (TC) in the mixed wastewater reach 91.5 % and 97.1 % in 90 min, respectively. Cyclic tests have shown that the electronic structure control exhibits excellent stability with removal ratios of CIP and TC of 83.9 % and 85.7 %, respectively. Finally, the 8C of CIP and the 11C and 19O of TC are most susceptible to the attack of free radicals generated by lattice compression spin polarization electric fields based on the theoretical calculations of the Fukui function and the analysis of intermediates. This work provides new insights into the design of catalysts for efficient photo generated charge dynamics with lattice strain.

Spin-anomalous-Hall unidirectional magnetoresistance in light-metal/ferromagnetic-metal bilayers

Nonreciprocal magnetotransport is one of the central topics in spintronics because of its importance for electrically probing magnetic information. Among numerous electrical probes used to read magnetic orders, unidirectional magnetoresistance (UMR), characterized by sign changes upon reversal of either current or magnetization, is currently a matter of great interest and has been identified in various spin–orbit-coupled bilayer systems composed of an (anti)ferromagnetic layer and a nonmagnetic layer with strong spin Hall effect. A recent theoretical work predicts that a spin-anomalous-Hall (SAH) UMR in those metallic conducting bilayers can originate from the spin-anomalous-Hall effect of the ferromagnetic layer and the structural inversion asymmetry. However, this type of UMR has not been reported experimentally. Here, we give the experimental evidence of spin-anomalous-Hall UMR in the light-metal/ferromagnetic-metal Cu/Co bilayers, where the emergence of net nonequilibrium spin density is attributed to the interfacial spin leakage asymmetry due to the spin memory loss effect at the Cu/Co interface and multiple spin reflections. We also show a highly tunable UMR in the Cu/Co/CuOx trilayer by varying the Cu thickness, which is due to the competition between the orbital Rashba effect in Co/CuOx and the spin-anomalous-Hall effect in Cu/Co. Our work widens the material choice for UMR device applications and provides an alternative approach to detect in-plane magnetization without an external spin polarizer.

Even-integer quantum Hall effect in an oxide caused by a hidden Rashba effect.

In the presence of a high magnetic field, quantum Hall systems usually host both even- and odd-integer quantized states because of lifted band degeneracies. Selective control of these quantized states is challenging but essential to understand the exotic ground states and manipulate the spin textures. Here we demonstrate the quantum Hall effect in Bi2O2Se thin films. In magnetic fields as high as 50 T, we observe only even-integer quantum Hall states, but there is no sign of odd-integer states. However, when reducing the thickness of the epitaxial Bi2O2Se film to one unit cell, we observe both odd- and even-integer states in this Janus (asymmetric) film grown on SrTiO3. By means of a Rashba bilayer model based on the ab initio band structures of Bi2O2Se thin films, we can ascribe the only even-integer states in thicker films to the hidden Rasbha effect, where the local inversion-symmetry breaking in two sectors of the [Bi2O2]2+ layer yields opposite Rashba spin polarizations, which compensate with each other. In the one-unit-cell Bi2O2Se film grown on SrTiO3, the asymmetry introduced by the top surface and bottom interface induces a net polar field. The resulting global Rashba effect lifts the band degeneracies present in the symmetric case of thicker films.

Evolution of structure, magnetism, and electronic/thermal-transports of Ti(Cr)-substituted Fe2CrV all-d-metal Heusler ferromagnets

All-d-metal full-Heusler alloys possess superior mechanical properties and high spin polarization, which would play an important role in spintronic applications. Despite this, their electrical and thermal transport properties have not been comprehensively investigated till now. In this work, we present an analysis on the evolution of structural, magnetic and transport properties of Cr- and Ti-substituted Fe2CrV all-d-metal Heusler alloys by combining theoretical calculations and experiments. Both series of alloys crystallize in Hg2CuTi-type structure. With increasing Ti doping, the calculated total magnetic moments of Fe50Cr25V25-xTix decrease linearly. The experimental saturation magnetization is highly consistent with theoretical calculations and Slater-Pauling rule when x < 4, indicating the highly ordered atomic occupation. The magnetization and Curie temperature can be significantly tuned by altering spin polarizations and exchange interactions. The introduction of the foreign atom, Ti, results in a linear increase in residual resistivity, while electron-phonon scattering keeps relatively constant. The maximum values for electrical and thermal transport properties are observed in the stoichiometric Fe2CrV composition.

Exploring spin current and dielectric switching characteristics of doped-multiferroic in hexagonal phase for advance RAM technology: A theoretical study

The single-phase bismuth ferrite BiFeO3 (BFO) has garnered significant interest due to its spintronic-based switching properties observed at room temperature. The first-principles calculations were executed to examine the spin-polarized electronic, dielectric, and structural characteristics of co-doped BFO with lanthanum (La) at A-site and cobalt (Co), nickel (Ni) at B-site in its hexagonal phase (Bi1-αLaαFe1-βNiβO3 with α = β = 0.04) with generalized gradient approximation (GGA-PBE). The highest value (1.01 × 10−11 A) of total current observed in La Ni co-doped BFO, featuring a distinct spin current of the same magnitude, attributed to spin polarization at the Fermi level (100 %). Additionally, Co-doped BFO exhibits the highest observed spin current density (1.05 × 109A/m2) and charge current density (1.03 × 10−5A/m2). In case of dielectric switching properties, the Ni-doped BFO displays the lowest values of linear dielectric polarization (6.00 × 10−2 C/m2), polarization charge at its interface (1.27 × 10−17 C), capacitance (4.23 × 10−15 F), and switching energy (3.81 × 10−19 J), which is particularly lower than the reported switching energy (1.92 aJ) of multiferroic capacitor.

Theoretical perspectives on the electronic, optical, mechanical, magnetic, and anisotropic behaviors of the quaternary Heusler alloys RhFeMnZ and IrMnCrZ (where Z = Si, Ge)

High-spin-polarised materials are the most promising candidates for spintronic devices. Here, the spin-polarised electronic structure, magnetism, mechanical, and optical properties of RhFeMnZ and IrMnCrZ (where Z = Si, Ge) Quaternary Heusler alloys were calculated by first-principles calculations. The calculations show that type III for the RhFeMnSi, RhFeMnGe, and IrMnCrSi and type I for the IrMnCrGe compound configuration is the most stable crystal structure for the studied alloys. The four alloys were found to have a half-metallic ferromagnetic structure with indirect band gaps in the majority spin channels of 0.957, 0.66, 0.745, and 0.891 eV for RhFeMnSi, RhFeMnGe, IrMnCrSi, and IrMnCrGe, respectively. They exhibit an appreciable total magnetic moment of 4 μB for RhFeMnZ (Z = Si, Ge) and 2 μB for IrMnCrZ (Z = Si, Ge). The results show that RhFeMnZ and IrMnCrZ (where Z = Si, Ge) are ferromagnetic half-metals with 100 % spin polarisation. The results of the elastic constants demonstrate the mechanical stability of RhFeMnZ and IrMnCrZ (where Z = Si, Ge) alloys. Optical properties such as dielectric function, absorption, reflectance, optical conductivity, and other optical properties were also probed. In the ultraviolet region, RhFeMnZ and IrMnCrZ (where Z = Si, Ge) are effective absorbers and have a high refractive index. Alloys are promising candidates for potential applications in spintronic devices.

Ultrafast spin transfer and its impact on the electronic structure.

Optically induced intersite spin transfer (OISTR) promises manipulation of spin systems within the ultimate time limit of laser excitation. Following its prediction, signatures of ultrafast spin transfer between oppositely aligned spin sublattices have been observed in magnetic alloys and multilayers. However, it is known neither from theory nor from experiment whether the band structure immediately follows the ultrafast change in spin polarization or whether the exchange split bands remain rigid. We show that ultrafast spin transfer occurs even in ferromagnetic gadolinium metal. Charge transfer between localized surface and extended valence-band states leads to a decrease of the surface spin polarization. This synchronously alters the exchange splitting of the bulk valence bands during laser excitation. Moreover, the onset of demagnetization can be tuned by over 200 fs by changing the temperature-dependent spin mixing. Our results show a promising route to ultrafast control of the magnetization, widening the impact and applicability of OISTR.

Charge Transfer and Intersystem Crossing in Compact Naphthalenediimide-Phenothiazine Triads: Synthesis and Study of the Photophysical Property with Transient Optical and Electron Paramagnetic Resonance Spectroscopic Methods.

In order to obtain a long-lived charge separation (CS) state in compact electron donor-acceptor molecular systems, we prepared a series of naphthalenediimide (NDI)-phenothiazine (PTZ) triads, with phenylene as the linker between the donor and acceptor. Conformation restriction is imposed to control the mutual orientation of the NDI and PTZ units by attaching methyl groups on the phenylene linker to tune the electronic coupling between the donor and the acceptor. Moreover, the PTZ moiety was oxidized to sulfoxide to tune the ordering of the CS state and the 3LE state (LE: locally excited state). UV-vis absorption spectra indicate electronic coupling between NDI with the phenylene linker as well as the PTZ units, manifested by the appearance of a charge-transfer (CT) absorption band, whereas this coupling is devoid in the triads with conformation restriction imposed. Fluorescence is strongly quenched in the triads compared to the reference compound, indicating electron transfer upon photoexcitation. Femtosecond transient absorption spectra indicate that the CS takes 0.8 ps, and then the 3LE state is formed by charge recombination in 83 ps. Nanosecond transient absorption (ns-TA) spectra show that the 3NDI state was observed in nonpolar solvents such as cyclohexane (triplet state lifetime: 95.7 μs), whereas the CS state was observed in more polar solvents. The CS state lifetimes are up to 1.2 μs (in toluene). Time-resolved electron paramagnetic resonance spectra of the triads in toluene consist of two types of signals: CS states (narrower signals, ∼10 mT) and 3LE states (broader signals, ∼50 to 200 mT). In the spectra of the triads containing PTZ, the CS state signals dominate, whereas for the triads containing oxidized PTZ, the 3NDI signals (zero-field splitting D ≈ 2000 MHz) prevail, both observations being in agreement with the ns-TA spectral studies. The electron spin polarization phase pattern of the 3NDI states of the triads indicates that the intersystem crossing (ISC) mechanism is spin-orbit charge-transfer ISC. Considering the 3CS state as ion pairs, the electron-exchange energy (J) is determined to be -39 to -59 MHz, and the electron spin dipolar interaction is 83-92 MHz.

Multiple Pathways in the Triplet States Population for a Naphthalenediimide-C60 Dyad.

The link of an antenna dye with an electron spin converter, in this case naphthalenediimide and C60, produces a system with a rich photophysics including the detection of more than one triplet state on the long timescale (tens of μs). Beside the use of optical spectroscopies in the ns and in the fs time scale, we used time-resolved Electron Paramagnetic Resonance (TREPR) to study the system evolution following photoexcitation. TREPR keeps track of the formation path of the triplet states through specific spin polarization patterns observed in the spectra. The flexibility of the linker and solvent polarity play a role in favouring either electron transfer or energy transfer processes.

Chemically Accurate Singlet-Triplet Gaps of Arylcarbenes from Local Hybrid Density Functionals.

Singlet-triplet (ST) gaps are key descriptors of carbenes, because their properties and reactivity are strongly spin-dependent. However, the theoretical prediction of ST gaps is challenging and generally thought to require elaborate correlated wave function methods or double-hybrid density functionals. By evaluating two recent test sets of arylcarbenes (AC12 and AC18), we show that local hybrid functionals based on the "common t" local mixing function (LMF) model achieve mean absolute errors below 1 kcal/mol at a computational cost only slightly higher than that of global hybrid functionals. An analysis of correlation contributions to the ST gaps suggests that the accuracy of the common t-LMF model is mainly due to an improved description of nondynamical correlation which, unlike exchange, is not additive in each spin-channel. Although spin-nonadditivity can be achieved using the local spin polarization alone, using the "common", i.e., spin-unresolved, iso-orbital indicator t for constructing the LMF is found to be critical for consistent accuracy in ST gaps of arylcarbenes. The results support the view of LHs as vehicles to improve the description of nondynamical correlation rather than sophisticated exchange mixing approaches.

Regulation of chiral structure and spin polarization by circularly polarized light and electric field in copolymers

Combining chirality with ferromagnetism is challenging in organic materials and may bring potential application for the cross-integration of multiple disciplines. In this work, we achieved the intrinsic coexistence of chirality and spontaneous spin polarization in the diblock copolymers, where left-handed and right-handed circularly polarized lights present tunability on both the circular dichroism and spin polarization. Without electron dependence of transport in chiral copolymer, chirality is still coupled with spin. The phenomenon observed here is not the traditional chirality induced spin selectivity effect. Moreover, the electric field could also effectively tune the chirality dependence of circular dichroism to further affect the magnitude of spin polarization. Thus, a strong relationship between the chirality and spin polarization is formed in chiral copolymers. In addition, because of the different molecular packing for chiral enantiomers, electron–phonon coupling strengths are different to lead to a difference in spin polarization. Overall, the properties of chirality, spontaneous spin polarization, and photon-chirality-spin coupling are developed and studied, which effectively promotes the ability of potential applications of chiral copolymers.

Investigating Structural, Mechanical, Electronic and Magnetic Properties of Spin-Gapless Quaternary Heusler Alloy Crmnval

Utilizing density functional theory (DFT), the study thoroughly investigates the equiatomic quaternary Heusler compound CrMnVAl, revealing its promising properties across multiple domains. The energy minimization curve shows its structural stability with lattice parameter 5.91Å in ferromagnetic phase. The negative values of formation and cohesive energy indicate its chemical stability, while electronic structure analysis demonstrates spin gapless semiconducting behavior. The total spin magnetic moment of this compound is almost 3.00 μB obeying the Slater-Pauling 18 electron rule (Mt = Zt – 18). The 100% spin polarisation and the Curie temperature higher than ambient temperature indicate that this compound acts as a promising material for spin dependent applications. Furthermore, exploring its mechanical properties complements these findings, offering insights into its structural integrity and suitability for diverse applications. Overall, the study underscores CrMnVAl's potential as a versatile material for spintronics and beyond.

Robust Ferrimagnetism and Ferroelectricity in 2D ɛ-Fe2O3 Semiconductor with Ultrahigh Ordering Temperature.

2D single-phase multiferroic materials with the coexistence of electric and spin polarization offer a tantalizing potential for high-density multilevel data storage. One of the current limitations for application is the scarcity of the materials, especially those combine ferromagnetism and ferroelectricity at high temperatures. Here, robust ferrimagnetism and ferroelectricity in 2D ɛ-Fe2O3 samples with both single-crystalline and polycrystalline form are demonstrated. Interestingly, the polycrystalline nanosheets also exhibit easily switchable ferroelectric polarizations comparable to that of single crystals. The existence of grain boundary does not hinder the switching and retention of ferroelectric polarization. Furthermore, the ɛ-Fe2O3 nanosheets show ferrimagnetic and ferroelectric Curie temperatures up to 800K, which reaches record highs in 2D single-phase multiferroic materials. This work provides important progress in the exploration of 2D high-temperature single-phase multiferroics for potentially compact high-temperature information nanodevices.

High polarization sensitivity passive spin Photogalvanic devices based on 2D perovskite CsMnBr4/CsSbCl3Br/CsMnBr4 heterojunction

In recent years, Dion-Jacobson (D-J) perovskite has been extensively studied. In order to further study the application of D-J perovskite materials in spin-optoelectronic multifunctional devices, this paper is based on CsSbCl3Br and CsMnBr4, a zero-band gap semi-metallic material with the same ferromagnetic ground state and the same crystal structure. In this paper, put forward with transverse CsMnBr4/CsSbCl3Br/CsMnBr4 heterojunction optoelectronic devices. The characteristics of photocurrent are discussed using parallel configuration (PC) and anti-parallel configuration (APC) magnetoelectric poles under two conditions: vertical incidence of linearly polarized light and elliptically polarized light utilizing density functional theory and the non-equilibrium Green’s function method. The results reveal that the device can achieve complete spin polarization photocurrent, pure spin current, perfect spin filtering effect, and excellent spin valve effect, with high extinction ratios. Under linearly polarized light, the maximum extinction ratio reaches 2747 for the PC configuration and 5200 for the APC configuration. For elliptically polarized light, the extinction ratio is 739 for the PC configuration and reaches a maximum of 240 for the APC configuration. These results indicate that the lateral CsMnBr4/CsSbCl3Br/CsMnBr4 heterojunction has broad multi-functional application prospects in the field of optoelectronics and spintronics.

Spin Polarization Enhances the Catalytic Activity of Monolayer MoSe2 for Oxygen Reduction Reaction.

The key factors in achieving high energy efficiency for proton exchange membrane fuel cells are reducing overpotential and increasing the oxygen reduction rate. Based on first-principles calculations, we induce H atom adsorption on 4 × 4 × 1 monolayer MoSe2 to induce spin polarization, thereby improving the catalytic performance. In the calculation of supercells, the band unfolding method is used to address the band folding effect in doped systems. Furthermore, it is evident from analyzing the unique energy band configuration of MoSe2 that a higher valley splitting value has better catalytic effects on the oxygen reduction reaction. We believe that the symmetries of the distinct adsorption site result in different overpotentials. In addition, when an even number of hydrogen atoms is adsorbed, the monolayer MoSe2 has no spin polarization. The spin can affect the electron transfer process and alter the hybrid energy with the reaction products, thereby regulating its catalytic performance.

Structural, mechanical, electronic, magnetic, optical, and thermoelectric properties of a new equiatomic quaternary heusler compound FeZrCrZ (Z = Si, Ge, Sn): A first-principles investigation

In this investigation, we undertake an ab initio exploration of the structural, mechanical, electronic, magnetic, optical, and thermoelectric characteristics of equiatomic quaternary Heusler compounds (EQH), specifically FeZrCrZ (Z = Si, Ge, Sn). Our investigation involves the utilization of the full-potential linearized augmented plane wave method (FP-LAPW) in density functional theory (DFT) framework, employing the generalized gradient approximation (GGA). The findings reveal that the Y-type-I arrangement, demonstrating ferromagnetic alignment, emerges as the most thermodynamically favored configuration among all FeZrCrZ (Z = Si, Ge, and Sn) compounds. Computed values for formation energy substantiate the feasibility of experimental synthesis.Furthermore, we meticulously determine elastic constants, confirming the structural robustness of the quaternary compounds. Dynamic stability analysis reinforces their stability. Electronic property assessments unveil the semi-metallic nature of FeZrCrZ (Z = Si, Ge, and Sn) alloys, showcasing complete spin polarization at the Fermi energy (100 %), a minimal energy gap, and magnetic moments of 2 μB when Z = Si, Ge, and 4 μB when Z = Sn. Optical property calculations encompass complex refractive index, dielectric function, reflectivity, absorption coefficient, and optical conductivity, indicating potential suitability of these compounds for optoelectronic applications. Employing Boltzmann transport theory, we investigate the thermoelectric performance of the compounds concerning temperature, and chemical potential. Evaluation of the thermoelectric response underscores their viability as thermoelectric materials, linked to a substantial figure of merit, increased Seebeck coefficient, and diminished thermal conductivity. This study provides crucial theoretical insights for experimental researchers, offering valuable information for the synthesis and application of these compounds in spintronics, thermoelasticity, and optoelectronics.

Anchoring Atomically Precise Chiral Bismuth Oxido Nanoclusters on Gold: The Role of Amino Acid Linkers.

The adsorption of chiral molecules onto metallic surfaces triggers electron spin polarization at the interface, paving the way for applications in chiral opto-spintronics. However, the spin effects sensitively depend on the binding and ordering of the chiral species on surfaces. This study explores the adsorption of chiral thioether-functionalized atomically precise bismuth oxido nanoclusters (BiO-NCs) on gold (Au) surfaces, extending the conventional approach of using thiol-containing molecules and complexes to nanoclusters. Starting from the precursor [Bi38O45(NO3)20(dmso)28](NO3)4·4dmso (A), chiral BiO-NCs were synthesized by substituting the nitrates with N-(tert-butoxycarbonyl)-l-methionine (Boc-l-Met-O-) ligands to obtain [Bi38O45(Boc-l-Met-O)24] (2). The full exchange of nitrate by the Boc-l-methionine ligand was demonstrated by powder X-ray diffractograms, dynamic light scattering, electrospray ionization mass spectrometry, nuclear magnetic resonance, infrared, circular dichroism, and X-ray photoelectron spectroscopy. Compared to previously reported [Bi38O45(Boc-l-Phe-O)24(dmso)9] (1), BiO-NC 2 shows differences in the growth mode on a Au surface as revealed by scanning electron microscopy, wherefore a stronger binding of BiO-NC 2 is assumed. Anchoring of BiO-NC 2 to the Au surface through thioether groups induced a discernible change in the optical response of the Au surface analyzed by spectroscopic ellipsometry (SE). From the numerical modeling of the SE parameters, a layer thickness of ∼2 nm, corresponding to a monolayer of BiO-NC 2, was estimated for the samples prepared by dip coating. Thus, strong adsorption of BiO-NC 2 to the Au surface is concluded, which is an essential prerequisite for chiral-induced interface spin polarization.