Role Of Titanium Research Articles

The role of titanium at the interface of hematite photoanode in multisite mechanism: Reactive site or cocatalyst site?

The role of titanium at the interface of hematite photoanode in multisite mechanism: Reactive site or cocatalyst site?

First Principles Modelling of Growth of Hybrid Organic-Inorganic Films

Hybrid organic-inorganic materials fabricated with molecular layer deposition (MLD) are a special class of materials that are attracting great interest in many economically and socially relevant technological applications due to their diphasic and tunable organic-inorganic structure. Despite the growing interest in these hybrid materials, knowledge around relevant precursor chemistries and reaction mechanisms, as well as details of many determined experimental results are unknown. Density functional theory (DFT) has proven to be a powerful tool to investigate and understand the atomic level details of the precursor chemistry and address aspects of the MLD experiments.In our work, we use first principles DFT calculations to examine key steps in the mechanism of hybrid film deposition through MLD by modelling precursor-surface and precursor-precursor reactions. We explore the growth mechanism of aluminium and titanium containing hybrid films, namely alucones and titanicones. Both materials are of high interest for passivation layers in batteries. For alucones we investigate in detail the chemistry of the MLD process between the post-trimethylaluminium (TMA) pulse methyl-terminated Al2O3 surface with aromatic compounds with hydroxy and/or amino groups as reactive groups: hydroquinone (HQ), 4-aminophenol (AP) and p-phenylenediamine (PD). Double reactions of HQ, AP and PDA with the Al2O3 surface are explored in detail to assist the interpretation of the experimental findings regarding the differences found for hybrid films grown with aromatic and aliphatic organic precursors. DFT calculations show that in contrast to aliphatic organics, an upright configuration will be present for HQ, AP and PD so that the molecules are self-assembled in an upright configuration, which leads to thicker hybrid films. We predict that aromatic molecules are the best choice for stable hybrid films and their chemistry can be manipulated without degrading stability. [1]We also investigate in detail the chemistry between the most common titanium precursors, namely titanium tetrachloride (TiCl4) and tetrakis(dimethylamido)titanium (Ti(DMA)4), and ethylene glycol (EG) and glycerol (GL) as the organic precursors for the fabrication of titanicone films. We analyse the impact of the substrate on the initial MLD reactions in titanicone film growth using three different surface models: anatase TiO2, rutile TiO2 and Al2O3. This work highlights the role of the phase of TiO2 and Ti-containing precursors in production of titanicone films and provides motivation to develop a new rutile TiO2 based hybrid film suggesting that the desired film growth, flexibility and stability can be achieved. [2][1] A. Muriqi, M. Karppinen and M. Nolan, Role of terminal groups in aromatic molecules on the growth of Al2O3-based hybrid materials, Dalton Transactions, 2021, 50, 17583-17593. doi.org/10.1039/D1DT03195C.[2] Arbresha Muriqi and Michael Nolan, “Role of Titanium and Organic Precursors in Molecular Layer Deposition of “Titanicone” Hybrid Materials”, Beilstein Journal of Nanotechnology, 2022, 13, 1240–1255. doi.org/10.3762/bjnano.13.103.

The Role of MX Carbonitrides for the Particle-Stimulated Nucleation of Ferrite in Microalloyed Steel

The role of titanium and vanadium carbonitrides (Ti,V)(C,N) of the MX series on the austenite-to-ferrite transformation in microalloyed steels and their potential of acting as pre-nuclei for intragranular ferrite nucleation is examined experimentally and by computational simulation. Thermal treatments and single-hit compression tests are performed on a dilatometer and a Gleeble® 3800 thermomechanical simulator to investigate the phase transition and precipitation sequences within microalloyed steel. The analysis of the microstructure and examination of formed precipitates is carried out by using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). In situ observations are realized via high-temperature laser scanning confocal microscopy (HT-LSCM). The experimental results are compared to kinetic precipitation simulations for MX precipitates’ particle-stimulated intragranular ferrite formation using an on-particle nucleation model for ferrite on the surface of the MX carbonitrides. A particular focus is the comparison of precipitation trends between non-deformed and deformed samples. The physically appropriate modeling of MX precipitation kinetics in combination with intragranular ferrite formation serves as a basis for future industrial process optimizations without extensive experimental work.

Role of Titanium in Ti/SiO2‐Supported Metallocene‐based Olefin Polymerization Catalysts. Part 2: Particle Fragmentation

AbstractA commercial SiO2 modified by the addition of a TiO2 layer on its surface and pore walls offers a support for metallocene‐based ethylene polymerization catalysts with a 35 % improved catalytic activity. The effect of such support modification on the catalyst particle fragmentation during polymerization reactions were assessed. This was performed by exposing the internal cross‐section of several SiO2 and Ti/SiO2‐based metallocene catalyst particles, polymerized at a wide range of reaction conditions, with a Focused‐Ion Beam Scanning Electron Microscope (FIB‐SEM), followed by a semi‐quantitative analysis of polymer, catalyst and macropores of each 2D image obtained. The titanation of the SiO2 lead to a support framework that fractures earlier and more efficiently. This was evidenced by the presence of several empty (polymer‐free) cracks along the support dense‐shell, found more extensively in the Ti‐modified polymerized catalyst particle, which also resulted in a more sustained polymerized particles macroporosity during the course of the reaction.

Role of Titanium in Ti/SiO2‐Supported Metallocene‐based Olefin Polymerization Catalysts. Part 1: Genesis of Active Sites and Catalytic Performance

AbstractPerformance enhancement of metallocene‐based olefin polymerization catalysts can be obtained, among others, by the chemical modification of their support. We investigated a titanated SiO2 (Ti/SiO2) as an improved support material for zirconocene catalysts, which lead to ∼35 % higher ethylene polymerization yields when compared to the unmodified SiO2‐supported metallocene. The improved catalytic performance of the modified catalyst was found to be related to the presence of a Ti‐based active site, second to the Zirconocene centers, as well as to a higher Lewis acidity in the titanated supported‐MAO, which improved the activation of the Zr‐based centers. The Ti active species were generated by reduction of the Ti/SiO2 support with the methylaluminoxane (MAO) co‐catalysts, which introduced oxygen vacancies (VO) and Ti3+ species, as confirmed by probe molecule Fourier Transform Infrared (FT‐IR) spectroscopy and UV‐Vis Diffuse Reflectance Spectroscopy (DRS). The higher Lewis acidity was linked to 5‐coordinated Ti4+, as detected by probe molecules FT‐IR spectroscopy.

Role of titanium and organic precursors in molecular layer deposition of "titanicone" hybrid materials.

The development of hybrid inorganic-organic films with well-controlled properties is important for many applications. Molecular layer deposition (MLD) allows the deposition of these hybrid films using sequential, self-limiting reactions, similar to atomic layer deposition (ALD). In this paper, we use first principles density functional theory (DFT) to investigate the growth mechanism of titanium-containing hybrid organic-inorganic MLD films, known as "titanicones". We investigate in detail the chemistry between the most common Ti precursors, namely titanium tetrachloride (TiCl4) and tetrakis(dimethylamido)titanium (Ti(DMA)4), and ethylene glycol (EG) and glycerol (GL) as the organic precursors. We analyse the impact of the substrate on the initial MLD reactions in titanicone film growth using three different surface models: anatase TiO2, rutile TiO2 and Al2O3. Calculated energetics show that while TiCl4 is reactive towards the anatase and rutile TiO2 surfaces, it is not reactive towards the Al2O3 surface. Ti(DMA)4 is reactive towards all surfaces. This is attributed to the stronger Ti-Cl bonds in TiCl4 compared to Ti-N bonds in Ti(DMA)4. Ti(DMA)4 also shows high reactivity to the organics compared to TiCl4. Double reactions of EG and GL with the TiCl3 species from TiCl4 and TiDMA species from Ti(DMA)4 are also explored to better understand the origin of the different thicknesses of EG-titanicone and GL-titanicone films observed in experimental work. We find that EG and GL coupled with TiCl4 can orient in a flat lying configuration on anatase while on rutile, the preferred orientation is upright. When combined with Ti(DMA)4, EG and GL prefer the flat lying configuration on all surfaces. This work shows that the choice of the surface and the metallic precursor has a major impact on the behaviour of organic species. DFT findings provide motivation to develop a low temperature rutile TiO2/titanicone film suggesting that the desired film growth could be achieved.

Prospects of Using Pseudobrookite as an Iron-Bearing Mineral for the Alkaline Electrolytic Production of Iron.

The alkaline electrolytic production of iron is gaining interest due to the absence of CO2 emissions and significantly lower electrical energy consumption when compared with traditional steelmaking. The possibility of using an iron-bearing pseudobrookite mineral, Fe2TiO5, is explored for the first time as an alternative feedstock for the electrochemical reduction process. To assess relevant impacts of the presence of titanium, similar electroreduction processes were also performed for Fe2TiO5·Fe2O3 and Fe2O3. The electroreduction was attempted using dense and porous ceramic cathodes. Potentiostatic studies at the cathodic potentials of −1.15–−1.30 V vs. an Hg|HgO|NaOH reference electrode and a galvanostatic approach at 1 A/cm2 were used together with electroreduction from ceramic suspensions, obtained by grinding the porous ceramics. The complete electroreduction to Fe0 was only possible at high cathodic polarizations (−1.30 V), compromising the current efficiencies of the electrochemical process due to the hydrogen evolution reaction impact. Microstructural evolution and phase composition studies are discussed, providing trends on the role of titanium and corresponding electrochemical mechanisms. Although the obtained results suggest that pseudobrookite is not a feasible material to be used alone as feedstock for the electrolytic iron production, it can be considered with other iron oxide materials and/or ores to promote electroreduction.

In Situ Investigation of the Cytotoxic and Interfacial Characteristics of Titanium When Galvanically Coupled with Magnesium Using Scanning Electrochemical Microscopy.

Recently, the cytotoxic properties of galvanically coupled Ti-Mg particles have been shown in different cells. This cytotoxic effect has been attributed mainly to Mg due to its tendency to undergo activation when coupled with Ti, forming a galvanic cell consisting of an anode (Mg) and a cathode (Ti). However, the role of the Ti cathode has been ignored in explaining the cytotoxic effect of Ti-Mg particles due to its high resistance to corrosion. In this work, the role of titanium (Ti) in the cytotoxic mechanism of galvanically coupled Ti-Mg particles was examined. A model galvanic cell (MGC) was prepared to simulate the Mg-Ti particles. The electrochemical reactivity of the Ti sample and the pH change in it due to galvanic coupling with Mg were investigated using scanning electrochemical microscopy (SECM). It was observed that the Ti surface changed from passive to electrochemically active when coupled with Mg. Furthermore, after only 15 min of galvanic coupling with Mg, the pH in the electrolyte volume adjacent to the Ti surface increased to an alkaline pH value. The effects of the galvanic coupling of Ti and Mg, as well as those of the alkaline pH environment, on the viability of Hs27 fibroblast cells were investigated. It was shown that the viability of Hs27 cells significantly diminished when Mg and Ti were galvanically coupled compared to when the two metals were electrically disconnected. Thus, although Ti usually exhibited high corrosion resistance when exposed to physiological environments, an electrochemically active surface was observed when galvanically coupled with Mg, and this surface may participate in electron transfer reactions with chemical species in the neighboring environment; this participation resulted in the increased pH values above its surface and enhanced generation of reactive oxygen species. These features contributed to the development of cytotoxic effects by galvanically coupled Ti-Mg particles.

Conversion of heavy gasoil into ultra-low sulfur and aromatic diesel over NiWRu/TiO2–γAl2O3catalysts: Role of titanium and ruthenium on improving catalytic activity

This contribution deals with about selective conversion of heavy gas oils into middle distillates fuels that meet ultra-low sulfur and aromatic compound quality standards by using a novel NiWRu/TiO2–γAl2O3catalyst under typical hydrotreatment conditions. A diesel fuel fraction having sulfur, nitrogen and aromatics compound content of about 50 ppm, 10 ppm and 15 v%, respectively, was obtained when the reactor was operated atT = 370 °C,P = 12.4 MPa, LHSV = 0.5 h−1and H2/hydrocarbon ratio = 800 Nm3/m3. Titanium and ruthenium additives used in the preparation of the NiWRu/TiO2–γAl2O3catalyst, remarkably improved the catalytic activities for the hydrogenolysis, hydrogenation and hydrocracking reactions compared to the reference NiW/γAl2O3catalyst. The coprecipitation of titanium and aluminum hydroxides produced a catalyst support having greater surface area, pore volume and surface acidity. An improvement in mechanical properties of the support extrudates was also observed. Characterization analysis by XPS, AUGER and XRD techniques of the TiO2–γAl2O3support suggested the formation of an aluminum-titanate mixed phase (AlxTiyOz) having a non-well-defined stoichiometry. The NiW/TiO2–γAl2O3and NiWRu/TiO2–γAl2O3exhibited a greater surface dispersion of the supported nickel and tungsten species compared to the NiW/γAl2O3catalyst. The promoter effect of ruthenium on the NiW bimetallic system caused a strong increase in both hydrogenolysis and hydrogenation reactions. Hydrodenitrogenation and hydrocracking reactions were also favored by the increase in the hydrogenation capacity and in the surface acidity of the catalyst. The highest conversion levels for all investigated reactions were obtained when the NiWRu/TiO2–γAl2O3catalyst was prepared by co-impregnation of Ni and Ru in a second step. This catalyst showed sulfur tolerance properties when the reaction was conducted in the presence of different H2S partial pressures. The catalytic behavior of the NiWRu/TiO2–γAl2O3catalyst was explained by the existence of a promoting effect between separated Ni and Ru sulfides species and the NiWS phase (dual mechanism).

The role of titanium on the microstructure and mechanical properties of additively manufactured C300 maraging steels

In this study, C300 metal powders containing two different Ti contents (0.72 and 1.17 wt%) were used to additively manufacture maraging steel samples in both horizontal and vertical directions via laser powder bed fusion (LPBF) technique. The effect of Ti addition on the microstructural and mechanical properties of the additively manufactured (AM) maraging steels was investigated using scanning, transmission electron microscopies (SEM, TEM), and electron backscatter diffraction (EBSD) along with uniaxial tensile and hardness testing procedures. Besides, X-ray diffraction (XRD) technique was employed to identify various phases formed during the LPBF process. The results showed that the horizontally printed Ti-rich samples exhibited higher retained austenite (γ) phase and superior values of hardness and tensile strength, while those ones vertically prepared showed an excellent ductility that could bring benefits in high-cycle fatigue applications. The TEM observations confirmed the presence of CoNi precipitates as well as high dislocation densities in the horizontal high Ti content samples, which are associated with higher strain hardening and tensile strength.

Role of titanium in bio implants and additive manufacturing: An overview

For many years titanium-based biomedical devices are gaining a promising place in modern society. Titanium is one of the best suitable materials for manufacturing bio implants and its application areas are orthopedics, dentistry etc. There are many features possess by titanium which make it appropriate are its biocompatibility, resistance to corrosion, wearing, osteoporosis etc. The Cp- Titanium and titanium-based alloys are categorized in three ways depending upon its microstructure such as (α + β), α- type, β-type and comparative analysis are done its behavior, stability through SEM. This review paper discussed the conventional and modern methods of fabricating the bio-implants and also summarizes the various additive manufacturing techniques.

Role of Titanium, Carbon, Boron, and Zirconium in Carbide and Porosity Formation during Equiaxed Solidification of Nickel-Based Superalloys

This work analyses the effect of Ti in the MC carbide formation and also in the γ/γ´ eutectic promotion in two nickel-based alloys melted under vacuum conditions and solidified into ceramic molds. The role of boron, carbon and zirconium on the porosity level after solidification of both alloys was also investigated; since the alloys were vacuum melted, it is assumed that the observed porosity is due to micro-shrinkage. The chemical compositions for two alloys were: 20.2Cr-13.7Co-4.78Mo-1.19Al-0.69Ti-0.08C-2.34Fe for Alloy 1, and 20.5Cr-15.6Co5.03Mo-1.57Al-3.42Ti-0.15C-1.64Fe-0.076Zr-0.01%B for Alloy 2. Results showed a higher volume fraction of MC carbides and the γ/γ´ eutectic for the Alloy 2 with higher titanium content since this element is a carbide and γ/γ´ eutectic promoter. The porosity level in the Alloy 2, with higher amounts of carbon, boron and zirconium was considerably lower than that for the Alloy 1. These results are discussed in terms of different phenomena caused by the segregating effects of boron, carbon and zirconium towards the interdendritic regions and the formation of zirconium carbides that produce an expansion in volume when they are formed at the end of the solidification process.

The efficiency analysis of grain refinement in high-zinc aluminium alloys with Ti-containing master alloy

ABSTRACTThe paper concerns double high-zinc aluminium alloys inoculated with master alloys containing titan and comprises research on the influence of inoculation on grain refinement. Most aluminium alloys before being cast have relatively low strength properties and therefore a series of treatments are applied in order to improve these properties. One of the treatments is the grain fragmentation process, called grain refinement treatment that allows to improve material properties of alloy, improve the feeding properties during the casting solidification, as well as to obtain more robust machinability of casting. Al alloy with 20wt% Zn (AlZn20) was tested, inoculated with the addition of traditional master alloy AlTi3C0.15 before casting to the sand mould.The results obtained during the studies show nucleating activity of the master alloy, proved by reduced overcooling and recalescence on cooling curves. Additionally, the role of titanium in this process is explained.

The role of titanium and vanadium based precipitates on hydrogen induced degradation of ferritic materials

The hydrogen induced damage of generic Fe-C-Ti and Fe-C-V ferritic alloys was investigated to assess the influence of precipitates on the hydrogen sensitivity of a material. The precipitates, formed during heat treatment, were evaluated by scanning transmission electron microscopy (STEM). The hydrogen/material interaction was evaluated by: 1) melt and hot extraction to determine the total and diffusible hydrogen content, respectively, 2) permeation experiments to calculate the diffusion coefficient, 3) thermal desorption spectroscopy to determine the hydrogen trapping characteristics of the materials. Furthermore, two different types of hydrogen induced damage were evaluated, i.e. hydrogen assisted cracking and blistering, resulting from electrochemical hydrogen charging with and without the application of an external load, respectively. Evaluation of the hydrogen induced damage and the role of the precipitates was performed by combining optical microscopy, scanning electron microscopy (SEM), and electron backscatter diffraction (EBSD). An important though divertive role of diffusible hydrogen is observed in both damage mechanisms for the investigated microstructures. On the one hand, a large amount of diffusible hydrogen compared to strongly trapped hydrogen promotes hydrogen assisted cracking of materials, while on the other hand, the blistering phenomenon is delayed under such conditions.

The role of titanium in the initiation of localized corrosion of stainless steel 444

Titanium has been added to ferritic stainless steels to combat the detrimental effects of intergranular corrosion. While this has proven to be a successful strategy, we have found that the resulting Ti-rich inclusions present on the surface play a significant role in the initiation of other forms of localized corrosion. Herein, we report the effect of these inclusions on the localized corrosion of a stainless steel using macro and micro electrochemical techniques. Through the use of scanning electrochemical microscopy, we observe the microgalvanic couple formed between the conductive inclusions and passivated metal matrix. The difference in local reactivity across the material’s surface was quantified using a 3D finite element model specifically built to respect the geometry of the corrosion-initiating features. Combined with electron microscopy and micro elemental analysis, localization of other alloying elements has been reported to provide new insight on their significance in localized corrosion resistance.

Titanium in the Structure of Alkali Borosilicate Glasses

Vibrational spectroscopy is used to show that the effect of adding titanium to K2O–B2O3–SiO2 glasses differing by the ratio of the boron and alkali metal contents is different. This result reflects the change in the structural role of titanium in the glass and is important for evaluating the influence of titanium additions on the properties of alkali borosilicate glass in the process of improving the glassy matrix materials used for the immobilization of radwastes.

Role of iron in Na 1.5Fe 0.5Ti 1.5(PO 4) 3/C as electrode material for Na-ion batteries studied by operando Mössbauer spectroscopy

The role of iron in Na 1.5Fe 0.5Ti 1.5(PO 4)3/C electrode material for Na batteries has been studied by 57Fe Mossbauer spectroscopy in operando mode. The potential profile obtained in the galvanostatic regime shows three plateaus at different voltages due to different reaction mechanisms. Two of them, at 2.2 and 0.3 V vs Na +/Na 0, have been associated to redox processes involving iron and titanium in Na 1.5Fe 0.5Ti 1.5(PO 4)3. The role of titanium was previously elucidated for NaTi 2(PO 4)3 and the effect of the substitution of Fe for Ti was investigated with 57Fe Mossbauer spectroscopy. We show that iron is an electrochemically active center at 2.2 V with the reversible Fe 3+/Fe 2+ transformation and then remains at the oxidation state Fe 2+ along the sodiation until the end of discharge at 0 V.

Effect of titanium addition on shape memory effect and recovery stress of training-free cast Fe–Mn–Si–Cr–Ni shape memory alloys

The shape memory effect and recovery stress of cast Fe–17.2Mn–5.28Si–9.8Cr–4.57Ni (18Mn) and Fe–17.5Mn–5.29Si–9.68Cr–4.2Ni–0.09Ti (18Mn–Ti) alloys have been investigated by optical microscopy, scanning electron microscopy (SEM), electron backscattering diffraction (EBSD), and resistivity–temperature curves. The cast 18Mn and 18Mn–Ti alloys solidified as the ferritic mode for which liquid phase fully transforms into primary δ ferrite. The role of titanium is to indirectly refine the austenite through refining the primary δ ferrite. In this case, the austenitic grains of the cast 18Mn alloy were much bigger than that of the cast 18Mn–Ti alloy, although the two alloys underwent δ→γ phase transformation. Grain refinement suppresses the stress-induced ε martensitic transformation, and thus the shape memory effect of the cast 18Mn–Ti alloy is worse than that of the cast 18Mn alloy. On the contrary, the maximum recovery stress and the recovery stress at room temperature are higher for the cast 18Mn–Ti alloy annealed at 1073K for 30min than for the cast 18Mn alloy annealed at 973K for 30min, because grain refinement suppresses the relaxation of recovery stress caused by the plastic deformation and the stress-induced ε martensitic transformation during cooling process. It is difficult to obtain the training-free cast Fe–Mn–Si based shape memory alloys with excellent shape memory effect and high recovery stress only by grain refinement.

The role of titanium at the SrTiO3/GaAs epitaxial interface

We study the role of a Ti surface treatment applied to the As-terminated GaAs (001) substrate surface prior to SrTiO3 (STO) epitaxial growth by comparing STO/GaAs samples prepared with and without Ti interlayers. Reflection high energy electron diffraction, transmission electron microscopy and x-ray photoelectron spectroscopy are used to assess the structural and chemical properties of the layers and interfaces. Without Ti interlayer, a polycrystalline TiGa compound is formed near the interface. It significantly degrades STO structural properties. A Ti interlayer efficiently prevents the formation of this unwanted compound by limiting As desorption from the GaAs substrate during STO growth. It improves significantly the structural quality of the oxide layer.

Conversion Reaction Mechanism in Complex Systems: A Triple X-Ray Absorption Spectroscopy Study of Tisnsb, a Very Efficient Negative Electrode Material for Li-Ion Batteries

The lithium-ion battery negative electrode material TiSnSb shows excellent electrochemical performance related to its high capacity (550 mA h g–1) and rate capability over several hundred cycles at relatively high rate (2 C).1 Such very good electrochemical performances are related to the highly reversible conversion reaction mechanism of this compound, and can be largely improved by specific electrode and electrolyte formulation.2–6 Using complementary information from operando X-ray diffraction (XRD) and 119Sn Mössbauer spectroscopy, it was determined that during the first discharge, TiSnSb undergoes a conversion process leading to the simultaneous formation of Li-Sb and Li-Sn intermetallics. The corresponding electrochemical equation was thus proposed for complete reaction of Li: TiSnSb + 6.5 Li = Ti + Li3Sb + 0.5 Li7Sn2 In this equation, however, the role of titanium was only hinted, since no specific information on this metal was available. Moreover, the mechanism by which the charge process occurs in TiSnSb is not yet fully understood due to the amorphous feature of the charged electrode. Different hypotheses have been proposed, including the presence of a mixture of binary phases, or the formation of a ternary alloy close to TiSnSb. At his time, however, the precise mechanism remains elusive. In order to shed more light on the role of titanium in this mechanism, and to better understand the interplay of the two p-group metal during the complex electrochemical discharge/charge mechanism, a complete operando X-ray absorption spectroscopy study of the system at the absorption K-edges of the three metals was performed. Operando EXAFS data at the Ti K-edge (Fig. 1), obtained on self-supported electrodes of TiSnSb formulated with CMC, provided clear evidence of the formation of Ti metal nanoparticles at the end of the discharge, confirming the supposed conversion mechanism. Operando EXAFS data obtained with fully formulated electrodes at the Sb and Sn edges (Fig. 2) show the formation of the lithiated phases, in line with the expected mechanism. However, the different reaction paths observed by comparing the Sn and the Sb spectra suggest that the two metals do not react simultaneously, and that Sn-rich intermediates are formed through the discharge and again during the following charge. These results are very important to corroborate the effective conversion mechanism in such system, and shed more light on the interplay of the two p-group metals in such complex system. References (1) Sougrati, M. T.; Fullenwarth, J.; Debenedetti, A.; Fraisse, B.; Jumas, J.-C.; Monconduit, L. J. Mater. Chem. 2011, 21, 10069. (2) Wilhelm, H.; Marino, C.; Darwiche, A.; Monconduit, L.; Lestriez, B. Electrochem. Commun. 2012, 24, 89. (3) Marino, C.; Sougrati, M. T.; Gerke, B.; Pöttgen, R.; Huo, H.; Ménétrier, M.; Grey, C. P.; Monconduit, L. Chem. Mater. 2012, 24, 4735. (4) Zhang, W.; Ghamouss, F.; Darwiche, A.; Monconduit, L.; Lemordant, D.; Dedryvère, R.; Martinez, H. J. Power Sources 2014, 268, 645. (5) Sivasankaran, V.; Marino, C.; Chamas, M.; Soudan, P.; Guyomard, D.; Jumas, J.-C.; Lippens, P.-E.; Monconduit, L.; Lestriez, B. J. Mater. Chem. 2011, 21, 5076. (6) Marino, C.; Darwiche, A.; Dupre, N.; Wilhelm, H.; Lestriez, B.; Martinez, H.; Dedryvère, R.; Zhang, W.; Ghamouss, F.; Lemordant, D.; Monconduit, L. J. Phys. Chem. C 2013, 117, 19302. Figure 1