Free-standing nanoribbons of InAs quantum membranes (QMs) transferred onto a (Si/Mo) multilayer mirror substrate are characterized by hard x-ray photoemission spectroscopy (HXPS) and by standing-wave HXPS (SW-HXPS). Information on the chemical composition and on the chemical states of the elements within the nanoribbons was obtained by HXPS and on the quantitative depth profiles by SW-HXPS. By comparing the experimental SW-HXPS rocking curves to x-ray optical calculations, the chemical depth profile of the InAs(QM) and its interfaces were quantitatively derived with ångström precision. We determined that (i) the exposure to air induced the formation of an InAsO4 layer on top of the stoichiometric InAs(QM); (ii) the top interface between the air-side InAsO4 and the InAs(QM) is not sharp, indicating that interdiffusion occurs between these two layers; (iii) the bottom interface between the InAs(QM) and the native oxide SiO2 on top of the (Si/Mo) substrate is abrupt. In addition, the valence band offset (VBO) between the InAs(QM) and the SiO2/(Si/Mo) substrate was determined by HXPS. The value of VBO = 0.2 ± 0.04 eV is in good agreement with literature results obtained by electrical characterization, giving a clear indication of the formation of a well-defined and abrupt InAs/SiO2 heterojunction. We have demonstrated that HXPS and SW-HXPS are non-destructive, powerful methods for characterizing interfaces and for providing chemical depth profiles of nanostructures, quantum membranes, and 2D layered materials.
III-V compound semiconductors possess superior carrier transport and excellent optoelectronic properties, which render them widely used in high performance electronic and optoelectronic devices, such as high electron mobility transistors, heterostructure lasers, and solar cells.1–3 These III-V “alternative” semiconductors, such as InAs and InGaSb, have much higher electron/hole mobility than Si and are good candidates to replace Si as future channel materials in metal–oxide–semiconductor field-effect transistors (MOSFETs).4–7 However, the growth of these semiconductors and their integration with the low-cost processing of Si technology present challenges since high defect densities and junction leakage currents may occur at the interface between these compounds and the Si substrate8 due to their lattice mismatch. In order to overcome the problems related to the growth of these semiconductors on Si or SiO2 substrates and to their integration with the more mature Si-based processes, Javey et al.9 developed a method for transferring ultrathin free-standing crystalline III-Vs films on a user-defined substrate. This transfer step led to high-performance III-V complementary metal–oxide–semiconductor (CMOS) and radio frequency (RF) circuits on both Si and plastic substrates.10 However, the non-destructive characterization of these transferred films is still a challenge. In particular, their depth-resolved chemical composition and the intermixing/oxidation occurring at the interfaces have not been fully determined. Low- and high-resolution transmission electron microscopy (TEM) characterization on such membranes has been performed by Javey et al.11 However, it is well known that the sample preparation for TEM analysis can induce damages to the material and can create interdiffusion at the interfaces.12 Therefore, TEM has limitations as a technique for a non-destructive, quantitative characterization of the interfaces of quantum membranes. On the other hand, the characterization of these interfaces is fundamental for high performance nanoscale transistors. It is known that oxide layers on the surface,13 or at the interface, strongly influence the electronic transport properties of these materials, especially in the case of nanowires and quantum membranes. For instance, the native oxide layer could shift the position of the surface Fermi-level or even induce Fermi-level pinning, which significantly degrades device performances.14,15,11
In this paper, we show that hard x-ray photoemission spectroscopy (HXPS) and standing wave HXPS (SW-HXPS) can be used to characterize bulks and buried layers/buried interfaces without altering the samples. Standard XPS analysis provides information on the chemical and electronic states of each element at the surface. Moving to hard x-ray photon energies (2–15 keV), and thus to larger electron inelastic mean-free paths (IMFPs),16 allows one to obtain information on chemical and electronic states of the bulk and of the buried interfaces.17 Among the many III-V alternative semiconductors, we chose to study free-standing InAs quantum membranes [InAs(QM)] which, in addition to their interesting properties, represent a more general class of 2-D materials. For instance, it has been reported9,11 that when the thickness of InAs is reduced, especially when it is below its exciton Bohr radius (34 nm), strong quantum confinement effects start to emerge and its band structure can be precisely tuned from bulk to 2D by changing the thickness. In particular, we have studied by SW-HXPS the possible formation of a surface oxide layer and interdiffusion at the top and bottom interfaces of InAs(QM) nanoribbons. Furthermore, we have determined if and what kind of oxide layer is formed at the top vacuum/InAs interface and how abrupt the InAs/bottom layer interface is.
Schematic of the InAs(QM) nanoribbons transferred onto a (Si/Mo) × 80 multilayer (dimensions not to scale) on which the van der Waals attraction holds the InAs(QMs) in intimate contact. Each nanoribbon is 15 nm thick and 300 nm wide, and the distance between one ribbon and its neighbors is 300 nm. The multilayer period is 3.3 nm.
Schematic of the InAs(QM) nanoribbons transferred onto a (Si/Mo) × 80 multilayer (dimensions not to scale) on which the van der Waals attraction holds the InAs(QMs) in intimate contact. Each nanoribbon is 15 nm thick and 300 nm wide, and the distance between one ribbon and its neighbors is 300 nm. The multilayer period is 3.3 nm.
The InAs(QM) in the shape of nanoribbons was epitaxially grown on the GaSb/AlGaSb substrate along the [111] plane.9 Each nanoribbon is 15 nm thick and 300 nm wide, and the distance between one ribbon and its neighbors is 300 nm (Fig. 1). The (Si/Mo) multilayer onto which these InAs(QM) nanoribbons were transferred was prepared at the Center for X-ray Optics of the Lawrence Berkeley National Laboratory and consists of 80 (Si/Mo) bilayers, each bilayer having a thickness of 3.3 nm. The termination layer of this (Si/Mo) mirror was chosen to be Si, which, exposed to air, gives rise to a thin layer of native silicon oxide (SiO2). In this way, the bottom interface between the InAs(QM) and the SiO2/(Si/Mo) substrate is a good approximation to the interface between the InAs(QM) and a typical silicon-based substrate. Before transferring the InAs(QM) on it, the mirror was cleaned with acetone, isopropyl alcohol, and de-ionized water.9 At the photon energy of 4.0 keV used in our measurements, the Bragg angle is θBragg ≈ 2.7°. In order to scan over the first order Bragg reflection, the incidence angle of the incoming x-ray beam was varied between 2.4° and 3.5°, in steps 0.02°. The HXPS spectra were obtained at the Advanced Light Source (ALS) (Beamline 9.3.0) and at SOLEIL Synchrotron (GALAXIES Beamline).21 The p-polarized x-ray photon energy was set to hν = 4.0 keV, and the spectral total energy resolution was ≈500 meV for the data acquired at ALS and ≈250 meV for the data acquired at SOLEIL. At hν = 4.0 keV, the IMFP, as estimated from the TPP-2M formula,22 is ∼7 nm for InAs. As a consequence, not only the top surface but also the bottom interface between the InAs(QM) and the SiO2(Si/Mo) substrate could be characterized by HXPS. The geometry of the experiment is as follows: the angle between x-ray incidence and photoelectron exit is 90° and the incidence angle relative to the sample surface is 2.4°-3.0°. Thus, the photoelectron takeoff angle with respect to the surface is from 87.6° to 87.0° and essentially along the surface normal. The binding energies of the HXPS spectra were calibrated using Au 4f and Au EF before and after each data acquisition.
Figure 2 shows the relevant core level (CL) spectra of the InAs(QM) and of the SiO2/(Si/Mo) mirror. Various chemically shifted components are also indicated. Since the InAs(QM) sample was exposed to air before the HXPS analysis, the presence of C 1s is probably due to surface contamination. Although C 1s was fit with two components, their rocking curves (RCs) are identical; thus, there is only one effective depth for whatever C contaminant species are present.
Experimental x-ray photoelectron core level spectra for all of the elements in the InAs(QM) and the mirror substrate: C 1s, O 1s, As 2p3/2, In 3d5/2, Mo 3d, and Si 2p, with chemically shifted components indicated.
Experimental x-ray photoelectron core level spectra for all of the elements in the InAs(QM) and the mirror substrate: C 1s, O 1s, As 2p3/2, In 3d5/2, Mo 3d, and Si 2p, with chemically shifted components indicated.
Each of the As 2p, In 3d, Si 2p, and O 1s CL spectra shows clear evidence of two components. As reported in the literature,23,24 the As 2p shoulder at binding energy (BE) = 1326 eV and that of In 3d at BE = 446 eV are attributed to the presence of AsOx and InOx, and the weak Si 2p peak at BE = 103.5 eV is assigned to the native SiO2 on top of the (Si/Mo) mirror. The depth distribution of these elements and of their different valence states can be obtained by SW-HXPS, including the two O 1s components, the main peak at BE = 533.4 eV, and the shoulder at BE = 531 eV. The CL spectra were analyzed by subtracting a Shirley background25–27 from each spectrum before fitting it with Voigt functions. The peak integrated intensity of each CL was then plotted versus the incidence angle, thus generating what we call experimental rocking curves (RCs). The RCs so obtained are shown in Fig. 3(a) (data points). From these RCs, a qualitative picture of the chemical depth profile of the InAs(QM) nanoribbons can be obtained. All the RCs show a maximum or minimum at the incidence angle ≈2.7° that corresponds to the Bragg peak of the (Si/Mo) multilayer. In addition, we observe that the RCs can be grouped into four different categories: (1) the RC of C 1s, including its strong modulation, does not match with any other RCs. Its strong RC modulation suggests that C origins from a thin surface layer and probably is due to the exposure of the sample to air; (2) the RCs of the As 2p3/2 shoulder at BE = 1326 eV, of the In 3d5/2 shoulder at BE = 446 eV, and of the O 1s shoulder at BE = 531 eV are very similar in phase and intensity modulation, indicating that these In, As, and O atoms are at the same depth and suggesting the presence of an InAsOx layer; (3) the RCs of the As 2p3/2 main peak at BE = 1323 eV and of the In 3d5/2 main peak at BE = 445 eV are very similar in phase and intensity modulation, although their phase is opposite and their modulation is smaller than those of the RCs in group 2. This indicates the presence of an InAs layer thicker and at a different depth than the InAsOx layer. The lower modulation of the InAs layer is due to the large escape depth of the electrons, coupled with the high layer thickness of the InAs compared to the SW period, with the thickness extending over multiple periods of the SW; (4) the RCs of the O 1s main peak at BE = 531 eV and of Si 2p at BE = 104 eV show the same modulation and phase, confirming that the O 1s main peak is associated with the presence of the native SiO2 on top of the (Si/Mo) mirror.
(a) Experimental (○ data points) and calculated (- curves) RCs. (b) Summary of InAs(QM) nanoribbon’s depth profile.
(a) Experimental (○ data points) and calculated (- curves) RCs. (b) Summary of InAs(QM) nanoribbon’s depth profile.
In addition to this qualitative information, an analysis of the experimental RCs using an x-ray optical program, the Yang X-Ray Optics (YXRO) code,18,28 can provide more quantitative information on the depth, chemical state, composition, and interdiffusion of the four layers described earlier. As an input, the YXRO code requires the experimental geometry and the upper and lower limits for the sample structure parameters such as thickness and interdiffusion/roughness. In addition, in order to accurately predict the RCs, the YXRO code takes into account the sample optical parameters, the differential photoelectric cross sections, and the photoelectron IMFPs. A thorough description of the YXRO program and its theoretical framework is presented in the paper by Yang et al. in Ref. 18.
The calculated RCs reported in this paper were obtained by combining the YXRO code with a global black box optimizer29 in order to maximize the goodness of the fit and the speed of the fitting process. A conventional squared-deviation R-factor was used to judge the goodness of the fit as a function of the sample structural parameters: layer thicknesses and interface thicknesses. This combination of the two programs has led to an approximately 100-fold increase in the speed of analysis compared to prior hand fitting.28
Figure 3 shows the final results for the experimental RCs (data points) and calculated RCs (curves) obtained by YXRO combined with the optimizer. The comparison between the experimental and calculated RCs for the final best-fit parameters thus provides quantitative information on the constituent layers and on the interfaces, including mixing or roughness at the interface. The agreement between the experimental RCs and the simulations from our best-fit is remarkable [Fig. 3(a)]. The results from the optimized depth profile are reported in Fig. 3(b). The top layer of adventitious carbon is ≈1.5 nm thick and in good agreement with the C 1s core level relative intensity as simulated by the program Simulation of Electron Spectra for Surface Analysis (SESSA).30 The C 1s RC is special, in that there are two contributors, on top of the InAs(QM) and on top of the SiO2, but the vertical distance (≈17.1 nm) separating them is about (1.4 + 0.9 + 13.2 + 0.8) nm = 16.3 nm from the top layer and 0.8 nm from the bottom layer, and this is almost 5 periods of the SW = 16.6 nm. Thus, the intensities of these two layers add coherently in the RC. The top layer of InAs(QM) is oxidized, and it is ≈1.4 nm thick. The exposure to air of the InAs(QM) nanoribbons induced the formation of an oxidized layer on their top surface. Based on the binding energies from the chemical shift of the oxidized As 2p and oxidized In 3d peaks, as reported in the literature,23,24,31 we conclude that this layer is InAsO4. The remaining part of the nanoribbons consists of a stoichiometric InAs layer of ≈13.2 nm. The top interface between the InAsO4 and InAs layers is not sharp but has ≈1.0 nm interdiffusion. On the other hand, the bottom interface between the InAs(QM) and the SiO2/(Si/Mo) mirror is abrupt and the thickness of the native SiO2 on top of the mirror is ≈1.6 nm. We would like to point out that the thicknesses and interdiffusion calculated from fitting the rocking curves describe the structure with uncertainties of the order of 0.3 nm due to the vertical resolution of the SW period and with uncertainties of the order of 0.4 nm due to the YXRO-Optimizer process.
Having determined that there is negligible interdiffusion between the bottom InAs(QM) and the SiO2/mirror substrate, the valence band offset (VBO) between these InAs(QM) nanoribbons and the SiO2/(Si/Mo) substrate could be determined by HXPS, using the method originally introduced by Kraut et al.32,33
In conclusion, we have demonstrated that HXPS and SW-HXPS are powerful non-destructive methods that can be used to characterize the interfaces in novel materials and nanostructures such as quantum membranes. For instance, HXSP and SW-HXPS provided the stoichiometry, the depth, and the thickness of the oxide overlayer on these InAs(QM) nanoribbons, which acts as passivation layer, useful in order to prevent dangling bonds. In addition, SW-HXPS showed that the interface between the InAs(QM) and its oxidation layer is not sharp, indicating that some interdiffusion occurred and that the oxidation is not entirely homogenous. On the contrary, the bottom interface between the InAs(QM) and the substrate is atomically abrupt, which is a crucial prerequisite for successful applications of high performance nanoscale transistors. In addition, the VBO between these InAs(QM) nanoribbons and the SiO2/(Si/Mo) substrate was determined. The obtained value of 0.2 ± 0.04 eV is in good agreement with literature results giving a clear indication of the formation of a well-defined and abrupt SiO2–InAs heterojunction.
This work was supported by the US Department of Energy under Contract No. DE-AC02-05CH11231 (Advanced Light Source, Materials Sciences and Chemical Sciences Divisions) and by DOE Contract No. DE-SC0014697 through the University of California Davis (salary for C.T.K., M.G., and C.S.F.). C.S.F. has also been supported for salary by the Director, Office of Science, Office of Basic Energy Sciences (BSE), Materials Sciences and Engineering (MSE) Division, of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231, through the Laboratory Directed Research and Development Program of Lawrence Berkeley National Laboratory, through the APTCOM Project, “Laboratoire d’Excellence Physics Atom Light Matter” (LabEx PALM) overseen by the French National Research Agency (ANR) as part of the “Investissements d’Avenir” program, and from the Jülich Research Center, Peter Grünberg Institute, PGI-6. A.R. was funded by the Royal Thai Government, A.K. was awarded with graduate student researcher-work study and departmental fellowship for at UC Davis, and C.C. was funded by GAANN program through UC Davis Physics Department. Materials processing was supported by the Electronic Materials Program funded by the Director, Office of Science, Office of Basic Energy Sciences, Materials Sciences and Engineering Division of the U.S. Department of Energy, under Contract No. DE-AC02 05Ch11231. O.K. and H.B. acknowledge support by the Director, Office of Science, Office of Basic Energy Sciences (BSE), Chemicals Sciences, Geosciences and Biosciences, of the U.S. Department of Energy under Contract No. DE-AC02 05CH1123.