- Open Access
Sound velocity of hcp-Fe at high pressure: experimental constraints, extrapolations and comparison with seismic models
© Antonangeli; licensee Springer. 2015
Received: 18 September 2014
Accepted: 17 February 2015
Published: 13 March 2015
Determining the sound velocity of iron under extreme thermodynamic conditions is essential for a proper interpretation of seismic observations of the Earth’s core but is experimentally challenging. Here, we review techniques and methodologies used to measure sound velocities in metals at megabar pressures, with specific focus on the compressional sound velocity of hexagonal close-packed iron. A critical comparison of literature results, coherently analyzed using consistent metrology (pressure scale, equation of state), allows us to propose reference relations for the pressure and density dependence of the compressional velocity of hexagonal close-packed iron at ambient temperature. This provides a key base line upon which to add complexity, including high-temperature effects, pre-melting effects, effects of nickel and/or light element incorporation, necessary for an accurate comparison with seismic models, and ultimately to constrain Earth’s inner core composition.
Iron (Fe) has always attracted considerable interest in fundamental physics and chemistry, as well as materials science, due to its primary role in a great variety of technological applications. The physical properties of Fe at high pressure and high temperature also have unique relevance for Earth and planetary science, since all the telluric planets share the same basic layered nature: a central metallic core, made mostly of iron, surrounded by a silicate mantle and a thin, chemically differentiated crust. Thus, the experimental characterization and theoretical calculations of the physical properties of iron at relevant thermodynamic conditions are crucial in refining the chemical composition and dynamics of the Earth’s core and of telluric planetary cores more generally.
Direct sampling of the Earth’s deepest regions, including the core, is impossible. Amongst the remote sensing techniques we have to rely on, seismology is certainly one of the most direct. Conventional, radially averaged, one-dimensional seismic models, such as the Preliminary Reference Earth Model (PREM, Dziewonski and Anderson, 1981), provide a generalized description of the evolution of the sound velocities (V P and V S) and density (ρ) with depth. However, to derive an accurate compositional model, these seismic observations have to be combined with experiments or calculations constraining the density and elastic properties of highly compressed candidate materials. In this respect, compressional-wave (V P) and shear-wave (V S) sound velocities play a fundamental role, as two of the few parameters that can be directly compared with the seismic observations.
In the early 1950s, Birch used shock wave measurements to support the notion that the Earth’s core was mainly composed of iron (Birch, 1952). Since then, a large number of experimental and theoretical studies have addressed the sound velocities of solid iron at extreme conditions. Over the last 15 years, a great deal of effort has been devoted to the development of experiments capable of probing elasticity and sound velocity of opaque metallic samples at high static pressure, with iron providing much of the motivation. Current data sets, however, even including those based on indirect determinations, are generally limited to pressures of the order of 100 to 200 GPa at ambient temperature, and very few results exist at simultaneous high pressure and temperature. Most importantly, different studies are not always in agreement. Thus, even neglecting eventual corrections at high temperature, the extrapolations of results to the pressures of the Earth’s inner core (330 GPa < P < 360 GPa) come with large uncertainties. These limitations become very critical when attempting to estimate the nature and amounts of light elements, whose presence as impurities in the inner core is required to modify the density and velocity of iron to match seismic observations. For instance, models based on linear extrapolations of V P-ρ relation argue for about 2 wt% silicon alloyed with iron in the inner core (Badro et al., 2007; Antonangeli et al., 2010), while a recent model using a power law for the V P-ρ extrapolation leads to 8 wt% silicon (Mao et al., 2012).
In this paper, we intend to briefly review the techniques for sound velocity determinations. Literature data will be examined and compared to ultimately propose a reference for the pressure and density evolution of compressional sound velocity of hexagonal closed-packed (hcp) iron, the polymorph of iron observed to be stable at Earth’s inner core conditions (Tateno et al., 2010). Finally, the proposed velocity-density relationship will be discussed in relation to potential high-temperature effects.
Experimental techniques for sound velocity determination under static high pressure
In the 1950s, shock wave measurements provided the bulk sound velocity (V ϕ) of iron along the Hugoniot curve at multi-megabar pressure (Birch, 1952), and the compressional sound velocity of solid iron has been determined along the Hugoniot up to melting (approximately 205 GPa) (Brown and McQueen, 1986). Conversely, sound velocity measurements of iron under static compression turned out to be an experimental challenge.
Conventional pulse-echo ultrasonic techniques require sample dimensions large enough to avoid overlap of successive acoustic echoes and, hence, experimental volumes of several cubic millimeters, hardly compatible with experimentation at megabar pressures. As a result, the ultrasonic V P and V S have been reported for hcp-Fe at only 16.5 GPa (Mao et al., 1998). Gigahertz interferometry has been proposed as a possible solution to overcome these hindrances, but applications at very high pressure are still limited (e.g. Jacobsen et al., 2004). Only very recently, measurements of acoustic echoes in samples compressed in diamond anvil cells became possible thanks to the developments in time-resolved pump-probe techniques (laser ultrasonics), both in the nanosecond time scale (Chigarev et al., 2008) and in the picosecond time scale (Decremps et al., 2008). Measurements on iron provided V P and V S up to 23 GPa (Chigarev et al., 2008) and of the only V P up to 152 GPa (Decremps et al., 2014).
Another classical method to obtain elasticity and sound velocity of samples at high pressure is Brillouin spectroscopy (e.g. Murakami et al., 2012), for which application is limited to optically transparent specimens. Impulsive stimulated light scattering (ISLS) has been developed to enable measurements on metallic samples but is sensitive to surface properties, and data analysis is relatively complex (e.g. Crowhurst et al., 2006). Nonetheless, aggregate sound velocities of hcp-Fe have been determined up to 115 GPa with this method (Crowhurst et al., 2004).
It is only with the advent of third-generation synchrotron sources and the development of X-ray diffraction and scattering techniques in conjunction with the use of diamond anvil cells that systematic experiments on iron and iron alloys at megabar pressure have become possible. The first attempts to obtain information on elasticity and sound velocity of hcp-Fe were based on X-ray diffraction (XRD) techniques. Lattice strain relations obtained by radial diffraction measurements on non-hydrostatically compressed iron were analyzed to estimate the single-crystal elastic moduli, and hence the aggregate velocities, up to 220 GPa at ambient temperature (Mao et al., 1998). Alternatively, Rietveld refinement has been exploited to estimate the Debye-Waller factor and then to calculate the aggregate velocities starting from X-ray diffraction measurements on hcp-Fe up to 300 GPa and 1,200 K (Dubrovinski et al., 2001). Although such studies provide very valuable information, they only probe the sound velocities indirectly, relying heavily on interpretative schemes and assumptions in data analysis. Specifically, stress inhomogeneities resulting from grain-to-grain interaction in combination with effects of plastic deformation undermine the validity of the continuum elasticity theory used by Mao et al. (1998) to invert the single-crystalline elastic moduli from the measured lattice strain (Merkel et al., 2006; 2009), while the results of Dubrovinski et al. (2001) explicitly depend on the assumed relation between the Debye-Waller temperature factor and the aggregate elastic properties.
In the early 2000s, two phonon-probe techniques were developed, almost in parallel: nuclear resonant inelastic X-ray scattering (NRIXS or NIS) and inelastic X-ray scattering (IXS or HERIXS). NRIXS probes the partial projected phonon density of states of materials containing Mössbauer resonant isotopes. In the case of pure 57Fe, the total phonon density of states is probed. Amongst the various thermoelastic and vibrational parameters that can be derived, the Debye velocity can be obtained by a parabolic fit of the low-energy portion of the phonon density of states (Sturhahn and Jackson, 2007). Combining the measured Debye velocity with results from an equation of state (density and adiabatic bulk modulus), V P and V S can be determined. IXS, on the other hand, can be applied to any material and probes the momentum-resolved phonon dispersions. In the case of experiments on single crystals, the longitudinal and transverse sound velocities can be measured along any arbitrary direction, and all the independent elements of the elastic tensor can be obtained (e.g. Antonangeli et al., 2004a). V P and V S can then be derived by straightforward averaging. However, in the case of measurements on polycrystalline samples (as typically the case for experiments at very high pressures), the loss of directional information limits the measurements to the averaged phonon dispersions of the aggregate (Bosak et al., 2007). V P can be then obtained from a sine fit to the aggregate phonon dispersion and V S derived by combining the measured V P with results from an equation of state (density and adiabatic bulk modulus) (Antonangeli et al., 2004b), but data analysis and interpretation now depend on how well the data sample the linear part of the phonon dispersion and on the knowledge of sample texture (Bosak et al., 2007).
Pioneering studies by IXS (Fiquet et al., 2001) and NRIXS (Mao et al., 2001) on hcp-Fe are contradictory. The linear extrapolation of the V P-ρ relation proposed by IXS experiments up to 110 GPa (Fiquet et al., 2001) is in close agreement with shock wave determinations (Brown and McQueen, 1986), suggesting that anharmonic effects at high temperature are negligible (Birch’s law) and arguing for hcp-Fe slower than PREM at core densities. On the contrary, V P derived from the phonon density of states measured by NRIXS up to 153 GPa (Mao et al., 2001) plots higher than shock wave determination (Brown and McQueen, 1986), indicating possible temperature effects, and extrapolates at core pressures to V P higher than PREM. Later NRIXS and IXS studies, with progressively improved beamline performance (flux, focusing optics), improved statistics and improved sample environment (hydrostaticity and/or texture characterization), focused on anisotropy (Antonangeli et al., 2004b; Lin et al., 2010), high-temperature effects (Lin et al., 2005; Kantor et al., 2007; Antonangeli et al., 2008; Antonangeli et al., 2012; Ohtani et al., 2013), or effect of nickel and/or light element inclusion (Lin et al., 2003; Badro et al., 2007; Kantor et al, 2007; Gao et al., 2008; Fiquet et al., 2009; Antonangeli et al., 2010; Shibazaki et al., 2012; Kamada et al., 2014). In view of the specific characteristics of the two techniques and of the respective data analysis, today’s general consensus is that, for measurements on polycrystalline samples, IXS provides more reliable V P and NRIXS more reliable V S (the Debye velocity measured directly by NRIXS is more heavily weighted in the determination of V S, while V P determination is more dependent on the used equation of state; in comparison, IXS provides a direct determination of V P while V S depends on the choice of equation of state).
Density dependence of the compressional sound velocity in hcp-Fe
All the techniques discussed above have advantages and drawbacks. A critical discussion of each individual technique is beyond the scope of the present paper. In the following, we will only compare results obtained for polycrystalline hcp-Fe under static compression by different methods, with specific interest on the pressure and density dependence of the compressional sound velocity. Our choice in limiting detailed discussion to V P is mainly driven by the fact that comparison with seismic models is more straightforward for the case of V P than V S. This is because anharmonic and/or pre-melting effects at high temperature (e.g. Laio et al., 2000; Vočadlo et al., 2009; Sha and Cohen, 2010; Martorell et al., 2013), as well as the possible presence of fluid inclusion in the core (Vočadlo, 2007), or frequency-dependent viscoelastic relaxations (Jackson et al., 2000), are all expected to more strongly influence V S than V P.
Comparison of results obtained by the various techniques, and sometime even the comparison of results obtained by the same technique, is complicated by dissimilar experimental strategies, differences amongst sample materials (isotopic compositions, degree of hydrostaticity, powders vs. foils, textures), and use of different pressure scales or equations of state (EOS). All these aspects have to be borne in mind when confronting different data sets. To allow for the most direct comparison, following Sakai et al. (2011; 2014), we rescaled reported pressures to the Pt scale of Matsui et al. (2009), which yields results quite consistent with the pressure scale of Dewaele et al. (2004) and Fei et al. (2007). When not otherwise specified, we use a third-order Birch-Murnagan relation with V 0 = 22.468 Å3/unit cell (Dewaele et al. 2006), K 0 = 155 GPa and K’ = 5.37 (Sakai et al., 2014) as the reference hcp-Fe EOS. To account for temperature effects, at least within the limit of a quasi-harmonic approximation (Antonangeli et al., 2008), we opted for the so-called Birch’s diagram, a V P-ρ representation of the data.
IXS experiments on hcp-Fe have been conducted over the last 15 years at the European Synchrotron Radiation Facility (ESRF) (Fiquet et al., 2001; Antonangeli et al., 2004b; Antonangeli et al., 2012) and more recently at the Advanced Photon Source (APS) (Mao et al., 2012) and at Spring-8 (Ohtani et al., 2013). This gives us the opportunity to compare measurements performed over time with the same instrument with similar experimental strategies, as well as results obtained by the same technique at different synchrotrons, often involving dissimilar experimental strategies. Importantly, in all cases, diffraction patterns have been collected in situ to obtain directly the densities, and the measured velocities do not depend upon any assumption concerning the equation of state. These aspects greatly facilitate direct comparison and allow evaluation of the finer aspects of the measurements such as instrument operation, energy and momentum resolution, analyzer settings, and sample preferred orientation. For a direct comparison, we only considered the ambient temperature measurements, even for the more recent studies including data at simultaneous high-pressure and high-temperature conditions (Antonangeli et al., 2012; Mao et al., 2012; Ohtani et al., 2013).
The discussion of the different NRIXS studies is somewhat less straightforward, because an EOS is used to solve for V P from the measured Debye velocity and because of the different isotopic enrichment in the samples used (which becomes relevant when estimating the density from the pressure or the volume). We considered the reported V P without accounting for possible difference due to the use of different EOS or dissimilar data processing. When not directly measured (as in Mao et al. (2001) and in Lin et al. (2005)), the density has been estimated using the same EOS used for data analysis, in order to have values of V P and ρ internally consistent, but neglecting the possible influence of variations in isotopic enrichment. For studies reporting data at simultaneous high-pressure, high-temperature conditions (Lin et al., 2005), we only considered 300 K data. Figure 4 shows V P as a function of density obtained by NRIXS studies (Mao et al., 2001; Lin et al., 2005; Murphy et al. 2013; Gleason et al., 2013). More recent data sets (Murphy et al. 2013; Gleason et al., 2013) benefited from improved instrument performance and have been collected with improved counting statistics, as well as enhanced hydrostatic conditions, relative to earlier determinations. Furthermore, density has been directly measured by complementary X-ray diffraction experiments. However, the two data sets, while suggesting a similar slope for the V P-ρ relation, display the largest difference in the absolute values of the velocities. A direct consequence of this is that one data set extrapolates slightly above PREM (Gleason et al., 2013) while the other extrapolates well below PREM (Murphy et al. 2013) (see Figure 4). A possible cause for this apparent discrepancy might come from the fact that, in contrast to other NRIXS studies, sample isotopic enrichment (56.95 vs 55.845 g/mol of natural Fe) has been explicitly accounted for in density determination in the analysis of Murphy et al. (2013). After rescaling the reported density to those expected for natural Fe (dotted line in Figure 4), we observe a closer agreement, even if the trend from Murphy et al. (2013) is still slightly below the others.
Pulsed laser techniques, even though not systematically used, provide measurements of sound velocities at pressures exceeding the megabar and are complementary to synchrotron-based techniques in many ways. In particular, picosecond acoustics can be seen as the most direct technique for sound velocity measurements in DAC, at least to the extent that, as in conventional pulse-echo ultrasonics, it is based on travel time determination. One of the main current disadvantages of both ISLS and picosecond acoustics is that these laboratory-based techniques are not yet coupled with X-ray diffraction. Accordingly, these measurements are more largely dependent on specific choice of ruby pressure scale and iron EOS. Results obtained by ISLS (Crowhurst et al., 2004) and by picosecond acoustics (Decremps et al., 2014) are reported in Figure 5. Densities have been determined starting with the reported pressures and using the EOS by Mao et al. (1990), which is consistent with the old ruby scale, and then using our reference EOS to reassess the pressure values. We observe that ISLS and picosecond acoustics data sets are in close agreement and linearly extrapolate to values somewhat above PREM.
A reference for V P-ρ relation for hcp-Fe at 300 K
Combining results obtained by different techniques, each one with its own specific and often very dissimilar advantages and limitations, likely provides the most stringent constraints on the V P-ρ relation. Application of classic pulse-echo ultrasonic techniques in multi-anvil presses is feasible but challenging, and only a single measurement has been obtained on hcp-Fe, at the relatively low pressure of 16.5 GPa (Mao et al., 1998). As already mentioned, V P derived from XRD-based techniques suffers from model dependence, but data have been obtained up to pressures close to 300 GPa (Mao et al., 1998; Dubrovinski et al., 2001), supporting a linear dependence of V P with density. NRIXS measurements may provide the most accurate determination of V S (Murphy et al., 2013; Gleason et al., 2013), while V P values are more dependent on the choice of the EOS used in the data analysis. On general grounds, fitting the low-energy portion of the phonon density of state as a parabola, as commonly done, might lead to an underestimation of the Debye velocity (Chumakov, 2014). This, together with the fact that measurements are carried on isotopically enriched samples of higher atomic weight than natural iron (56.95 g/mol for 95% isotopically enriched 57Fe samples vs. 55.85 g/mol for natural iron), might explain, at least qualitatively, why NRIXS measurements yield V P values generally lower than those measured by other techniques. Furthermore, the most recent, and presumably most accurate, NRIXS measurements (Murphy et al., 2013; Gleason et al., 2013) are in disagreement in terms of V P determinations (see Figure 4). Accordingly, we will not use NRIXS results to constrain the V P-ρ relation. IXS in combination with XRD has been largely used to measure the aggregate compressional sound velocity as a function of density. Provided an adequate data collection strategy (energy and momentum resolution, number and relative positions of points to constrain the phonon dispersion curve) and controlled and limited texture of the samples (polycrystalline aggregates, as close as possible to an ideal randomly oriented powder), V P can be obtained with 1% to 2% precision. Amongst the various data sets present in literature, we will not make use of the result by Fiquet et al. (2001), as these pioneering measurements have been superseded by subsequent determinations using improved instrumentation. Similarly, we do not use the results by Mao et al. (2012), because they were obtained on a foil, with relaxed momentum resolution and non-ideal settings of the spectrometer. Furthermore, this last data set is the only one supporting a sub-linear dependence of V P on ρ, in contrast to all other determinations. Both ISLS and picosecond acoustics do not allow for parallel determination of the density (at least with currently available experimental setups), but provide direct determination of surface waves (ISLS) and acoustic echoes (picosecond acoustics) travelling across the sample. With accurate estimation of the sample thickness, picosecond acoustic methods may thus yield the most direct measurements of V P.
Extrapolation to inner core conditions and high-temperature effects
In this paper, we reviewed the experimental techniques and methodologies used to measure sound velocities in metals at megabar pressures, with specific focus on the compressional sound velocity of hcp-Fe. Each technique presents advantages and drawbacks. Being aware of these is of the greatest importance when assessing the robustness of each measurement and, all the more so, when comparing different data sets. A critical review of literature results, coherently analyzed using consistent metrology (pressure scale, equation of state of hcp-Fe), allows us to propose a reference for the V P-ρ relationship in hcp-Fe at 300 K that linearly extrapolates 3% to 4% above PREM (Figure 6). This provides the principal base line upon which to add complexity, including anharmonic effects at high temperature, pre-melting effects, effects of nickel and/or light element alloying, required for accurate reconciliation with seismic models. In particular, our results argue for combined effects of high temperature and inner core impurities (such as nickel and light elements) that slightly reduce V P of pure hcp-Fe at constant density. This can be potentially satisfied by assuming that both alloying and high temperature only very moderately lower V P, which, however, is not supported by recent results (Badro et al., 2007; Antonangeli et al., 2010; Sha and Cohen 2010; Mao et al. 2012; Martorell et al., 2013). Alternatively, and most likely, effects of impurities (combined effect of nickel and light elements) and high temperature counterbalance, the first increasing velocity at constant density (e.g. Antonangeli et al. 2010) and the second decreasing velocity at constant density (e.g. Sha and Cohen 2010), leading to slightly reducing overall sum.
DA acknowledges the financial support from the Center of Excellence (COE) programme of Tohoku University for his visit to Japan in February 2014 that provided the ground for the discussions that led to the ideas presented in this paper. The authors wish to thank FJ Ryerson for proofreading the manuscript. This work has been supported by the French National Research Agency (ANR) grant no. 2010-JCJC-604-01 (DA), the JSPS KAKENHI (Grant-in-Aid for Specially Promoted Research) Grant Number 22000002, and the Ministry of Education and Science of Russian Federation, Project 14.B25.31.0032 (EO).
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