In situ diffraction studies of magnesium silicate liquids
Primitive MgO–SiO2 liquids dominate the early history of the Earth and Terrestrial planets. The structures of these liquids and structure-dependent properties, such as viscosity and diffusion, are considered important in the evolution of these planets, however, MgO–SiO2 liquids are refractory and do not form glasses easily and it is difficult to measure the structure of these liquids. Container-less synthesis techniques have been used to produce glasses that range in composition from 50 to 33% SiO2, corresponding to the compositions of two important mantle minerals: enstatite and forsterite. The structure of these glasses has been determined using combined neutron and high-energy diffraction and show changes in the short-range order as a function of composition. These changes include a jump in Mg–O coordination number at the limit to the formation of the silicate network in forsterite composition glass. These results imply a similar change in the structure of the liquid. Accordingly, the structures of forsterite and enstatite liquids have been determined using high-energy X-rays and a specialized sample environment, a containerless levitator. The main qualitative structural differences between MgSiO3 and Mg2SiO4 glasses are also observed in the melt. Liquid MgSiO3 is interpreted as forming a relatively ‘strong’ network of SiO4 tetrahedra, whereas the Mg2SiO4 liquid is “fragile” and dominated MgO n (n = 4, 5, 6) polyhedra and highly mobile oxygen ions. The results differ significantly from previously reported X-ray diffraction data for liquid MgSiO3.
KeywordsForsterite Enstatite Pair Distribution Function Liquid Structure Silicate Network
The liquid state dominates terrestrial and planetary processes and the molecular structure of liquids controls the thermodynamic and transport properties that determine planetary evolution [1, 2, 3, 4, 5, 6]. Although probes of liquid structure are, therefore, essential for understanding the liquid state it is often challenging experimentally to observe the structure at the temperatures and pressures of geophysical interest. One method that is often used to investigate the structure of the liquid state is to study the properties of the vitreous forms of the liquids of interest. Glasses, however, are not necessarily direct analogues of liquids but reflect a complex path through the metastable supercooled regime before kinetic arrest at the glass transition [7, 8, 9, 10, 11]. The structure retained in the glass therefore depends on the glass thermal history. Furthermore, amorphous forms of the same material can be produced by different synthesis routes and these different forms can have different structures and differ also in their bulk thermodynamic properties [12, 13, 14], this is referred to as polyamorphism. One consequence of polyamorphism is that some systems may have abrupt changes in the liquid structure in the supercooled regime and even first-order transitions between different metastable or stable liquid phases [15, 16].
Glasses produced in the MgO–SiO2 system between the compositions of the two important mantle minerals forsterite and enstatite show changes in structure [17, 18] that coincides with changes in the relaxation properties of these glasses [19, 20]. These rheological changes reflect differences in the configurational entropy of the liquid and in the terminology of Angell this is a change in the liquid fragility [7, 21, 22]. Glasses corresponding to the composition of forsterite (Mg2SiO4), the most silica-poor glass studied in this system, is the most fragile, in other words it has a viscosity–temperature relation that departs from the Arrhenius law [19, 20]. The more silica-rich glasses, with 38–50 mole% SiO2 are stronger. The structure of the forsterite composition glass also differs from those that are more SiO2-rich, the mean coordination number for forsterite glass is 5.0 compared with 4.5 for the 38–50% SiO2 compositions [17, 23]. This increase in Mg–O coordination represents a change in the structural role of the silicate tetrahedron, it has been argued by Kohara that forsterite composition glasses (33% SiO2) represent the limit to the formation of a polymerised network of corner-shared SiO4 tetrahedra and that the increase in Mg–O coordination number reflects formation of a network for edge- and face-shared Mg–O polyhedra corner-shared with isolated SiO4 tetrahedra and Si2O7 dimers. Although there is no direct correlation between liquid fragility and liquid structure, the study of the MgO–SiO2 glasses at ambient pressure and temperature raises a series of intriguing questions that have motivated more recent attempts to probe the glass and liquid structure at extremes of temperature and pressure. First, the discontinuity in Mg–O coordination number might be seen in the relaxed stable liquid as a sharper transition between two different structured liquids. Secondly, at high pressure it is believed that higher coordination environments become more stable and so when liquids and glasses are compressed it is possible that the Mg–O coordination number would increase with the possibility that percolation domains of the Mg–O polyhedra are formed at the expense of the polymerized silicate network. In this contribution, we will outline a series of related studies that attempt to expand our understanding of the structure and structure-related properties of these geophysically important liquids. We will outline a series of in situ studies of the liquids at high temperature but at ambient pressure and also a series of high-pressure experiments performed at ambient temperature on a single magnesium silicate glass.
Liquids and glasses lack the long-range orientational and translational atomic order that characterizes the crystalline state; liquids possess short-range order and glasses and amorphous solids have both short- and intermediate range order [24, 25]. Short-range order is usually described by a probability function, the probability of finding an atom at a distance, r, from an atom at the origin and this is the radial distribution function ρ(r), often referred to as a pair distribution function. The pair distribution function is obtained by Fourier transformation of the total structure factor, S(Q), obtained from diffraction data from liquids, glasses and amorphous materials that is probed by radiation with wavelengths comparable to the inter-atomic separation [26, 27, 28, 29, 30, 31, 32].
Structural studies of liquids and glasses involve the elastic scattering of neutrons and X-rays and with the development of third generation synchrotron sources, there has been progress in highly penetrating “neutron” like X-rays of ∼100 keV  for the study of liquid and glass structure. These high-energy X-rays act as a bulk probe in the same way that thermal neutrons do and cover a wide Q-range, comparable to neutron instruments at spallation sources.
Various types of sample environment can be used in combination with high-energy X-rays for the study of liquid sand amorphous materials. Although the structure of liquids at elevated temperatures can be studied using a variety of furnace types, the temperature range is much lower than the melting point of refractory liquids such as magnesium silicates. Containers and furnaces also have crystalline diffraction peaks which make extraction of the diffuse scattering signal from a liquid or glass difficult. A new development is the use of containerless levitation furnaces. In these specialised sample environments there is no contribution to the scattering pattern from the furnace, although the sample size is small. A further advantage of containerless levitation is that supercooled liquids can be studied which is difficult or impossible with more conventional furnaces because the container induces nucleation. In the containerless levitator technique [35, 36], a bead of refractory sample material is placed on a water-cooled conical nozzle and levitated by a gas jet, the bead can be laser heated to temperatures of up to 3050 K . The absence of heterogeneous nucleate sites means that liquids can be supercooled up to a few hundred degrees below the stable liquidus curve. Below we discuss the results of diffraction studies on magnesium silicate liquids using containerless levitation and high-energy X-rays at the Advanced Photon Source. We have determined the structure of forsterite and enstatite composition liquids which are compared with the equivalent glasses.
Experiment and analysis
High-energy X-ray diffraction data were collected at the 11-ID-C beamline at the Advanced Photon Source, Argonne National Laboratory. High-energy X-rays (115 keV) combine the advantages of neutrons; a high penetration and ability to act as a bulk probe, with the small beam size, high flux and rapid acquisition time that can be expected from third-generation synchrotron X-ray sources. Correction procedures are straightforward since the complicated absorption and attenuation effects are largely eliminated because of the high incident energies. Diffraction data can be obtained to high values of scattering vector (Q), comparable to those achieved by neutron diffraction and a “pseudonuclear” X-ray static structure factor can be obtained by an independent atom approximation . The 11-ID-C beamline has provision for a conical levitation sample environment to be integrated into the diffraction beam line to obtain diffraction data for refractory oxide liquids.
The conical levitator uses aerodynamic levitation to raise a 2–3 mm drop of liquid above a purpose-designed, water-cooled conical nozzle. The sample is heated by a 240 W continuous wave CO2 laser and the entire levitator is enclosed in a stainless steel chamber with Kapton® windows that allow the sample environment to be operated in transmission mode. Diffraction patterns are collected using a MAR345 image plate detector mounted orthogonal to the incident beam. The X-ray structure factor is obtained using a software mask to eliminate the scattering contribution from the sample nozzle and the sample-detector distance and tilt angle of the detector are determined by refining a polycrystalline CeO2 standard. The S(Q) data, up to 16 Å−1, are obtained by applying standard correction procedures. Slowly varying slopes on the data are believed to be sample-dependent backgrounds which can result from differences in the scattering of hot gas and from slow evaporation of the sample during experiment. These long-wavelength slopes appear as sharp peaks at the lowest r values (<1 Å) in the pair correlation functions and were corrected for using the Krogh-Moe-Normal method .
Electron microprobe analysesa of post-levitation MgO–SiO2 beads
38.69 ± 0.16
0.55 ± 0.02
59.51 ± 0.20
56.65 ± 2.15
0.39 ± 0.39
41.21 ± 2.15
A comparison of the real space data for the glassy state can be used as a starting point in interpretation of the liquid structures . In the pair-distribution function (PDF) there are three major peaks. The Si–O contribution is known to be the first peak centred on 1.65 Å, in both liquid and glass diffraction data this first peak remains unchanged and is consistent with SiO4 as the main structural unit. The Mg–O peak is about 2.1 Å and overlaps with the Si–O peak. The shoulder at 3.0 Å is dominated by O–O correlations but the main peak contains several overlapping contributions from Mg–Mg, Si–Si and Mg–Si.
D(r) has a dominant Si–O peak centred at 1.65 Å for liquid MgSiO3. The Mg–O correlation shows up as a weak asymmetry to this peak at higher radial distances and is less distinct in the liquid than in the glass (Fig. 2). At greater distances, the peak at 3.0 Å is interpreted as O–O correlations and the shoulder at 3.3 Å is dominated by cation–cation correlations; and there is also a peak at 4.3 Å. At the forsterite composition (Fig. 2b) there is an increase in Mg–O coordination number in the glass, but in the liquid the Mg–O feature overlaps strongly with the Si–O peak. In the glass there is a sharp feature at 3.16 Å which in the liquid is replaced by two broad overlapping peaks that are resolved. The relative changes in height of the Si–O and Mg–O peaks in the liquid spectra as a function of composition are expected; however, since there is no change in the O–O peak this does not reflect a linear change in local structure. Rather the change with composition is similar to that observed in the glass, with an increase in intensity of the peak at 3.3 Å as the MgO content is increased. The 33% SiO2 (forsterite) liquid is therefore interpreted as being more disordered, consistent with an increase in the so-called fragility of this composition liquid.
The structure of MgO–SiO2 liquids
The peak at 1.55 Å−1 in liquid SiO2 is commonly referred to as the first sharp diffraction peak, and is characteristic of the so-called intermediate range order in network-forming glasses; in the case of SiO2 it has been associated with the formation of small cages which form the network structure [42, 43] with a periodicity on the length scale of (2π/Q FSDP) = 4–5 Å. Oscillations also persist in the SiO2 liquid data out to high values of Q, and the liquid SiO2 structure for temperatures up to 2100 °C suggests a persistence of the corner-shared SiO4 network with a slight expansion of the Si–O bond distance and a dominant number of open six membered rings in the high-temperature liquid. The liquid data for 51%MgO–49%SiO2, from the study of Waseda and Toguri , resembles that of the pure SiO2 data; the first peak has a high intensity and occurs at lower Q than the first peak in our MgSiO3 liquid data and the high Q features are more prominent. The MgSiO3 and Mg2SiO4 liquid spectra that we have studied have very weak features at high Q, indicating that the liquids are much more disordered than pure liquid SiO2. This together with the known asymmetry of the Mg–O correlations (Shinji) have prevented us from obtaining accurate coordination numbers directly from our data. Consequently, we suggest that the data of Waseda show characteristics of a more silica-rich composition indicating preferential loss of MgO driving the liquid towards the more SiO2-rich end of the phase diagram. No compositional analysis after the experiment was reported in Waseda’s earlier study.
The diffraction data and reverse Monte Carlo modelling of the more silica-rich glasses suggest that the structures of 33% SiO2 (forsterite) and enstatite (50% SiO2) glasses are different. Enstatite glass has magnesium in a mixture of MgO4 and MgO5 polyhedra which are corner-shared with SiO4 tetrahedra that are in a silicate network. Consistent with NMR data that suggest dominance by Q 2 in the more silica-rich glasses, while the species that dominates the 33% SiO2 glass is Q 0 (i.e. isolated SiO4 tetrahedra). There are differences in the thermodynamic properties of the glasses and these also correlate with the changing structural role of Mg–O. The glass-forming ability of the 33% SiO2 composition is poor and the liquid does not form a glass readily in contrast to the more silica-rich compositions in which glasses can be formed relatively straightforwardly by containerless techniques. This indicates a change in the underlying relaxation properties and is confirmed by differential scanning calorimetry. The 50% SiO2 glass is stronger; there is an increase therefore in configurational entropy in the 33% SiO2 composition. Similarly there are differences in the heat of vitrification . These observations imply a correlation between changes in the bulk thermodynamic properties (enthalpy, entropy and volume) at the limit of network glass formation suggested by Kohara .
The high-energy X-ray diffraction data for the liquids show a progressively weaker influence of the silicate network in the liquid and allow us to identify three classes of liquid in the modified phase diagram (Fig. 3). The fully polymerised SiO2 network, the MgSiO3 liquid with a sparse (Q 2) silicate network and the Mg2SiO4 liquid, where the silicate network is replaced by a percolation domain of Mg–O polyhedra. These different liquids are likely to become progressively more fragile, with the temperature dependence of liquid structure correlates with the increased oxygen mobility in the distorted local environment of magnesium. The forsterite composition liquid is the most fragile, as shown by calorimetric data and it is possible that, as with the glass, the transition from one liquid type (I) to another (II) may occur over a narrow compositional interval.
We have demonstrated the combination of containerless levitation and high-energy X-ray diffraction for binary oxide liquids. Although binary silicate systems are relatively simple and only crudely approximate natural silicate liquids, the diffraction data illustrate that the increased distortion of the local environment around magnesium ions can be correlated with the departure from Arrhenius law viscosity. We anticipate that this diffraction data will provide a rigorous test of molecular dynamics simulations on MgO–SiO2 melts, which have so far shown poor agreement with the glass pair distribution function [44, 45]. For liquids with 50% SiO2, corresponding to the composition of the mineral enstatite, the liquid comprises a sparse network of SiO4 tetrahedra with highly mobile magnesium ions although the silicate network controls the liquid rheology. For silica-poor liquids, such as the forsterite composition liquid there is no polymerised silicate network and the high-temperature liquid comprises a sea of highly mobile magnesium ions with isolated SiO4 units. The temperature dependence of this liquid reflects the increasing mobility of the magnesium ions and distortion of the Mg–O environment. Although these magnesium silicate liquids are of primary interest to the geological community they show features that allow a more generalised interpretation of oxide liquids to be made and this experimental approach, in situ diffraction measurements of the refractory liquids, can be used to establish the link between structure and the thermodynamic (configurational entropy) descriptions of liquid viscosity.
The experiments at Argonne National Laboratory were supported by the U.S. DOE under contract number DE-AC02-06CH11357. Electron microprobe analyses of the samples following the levitation experiments were performed by Dr S. L. Kearns, Department of Earth Sciences, University of Bristol and we gratefully acknowledge his help in these compositional analyses.
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