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We describe the first implementation of broadband, nanosecond time-resolved step-scan Fourier transform infrared (S2-FT-IR) spectroscopy at a pulse radiolysis facility. This new technique allows the rapid acquisition of nano- to microsecond time-resolved infrared (TRIR) spectra of transient species generated by pulse radiolysis of liquid samples at a pulsed electron accelerator. Wide regions of the mid-infrared can be probed in a single experiment, which often takes < 20–30 min to complete. It is therefore a powerful method for rapidly locating the IR absorptions of short-lived, radiation-induced species in solution, and for directly monitoring their subsequent reactions. Time-resolved step-scan FT-IR detection for pulse radiolysis thus complements our existing narrowband quantum cascade laser-based pulse radiolysis-TRIR detection system, which is more suitable for acquiring single-shot kinetics and narrowband TRIR spectra on small-volume samples and in strongly absorbing solvents, such as water. We have demonstrated the application of time-resolved step-scan FT-IR spectroscopy to pulse radiolysis by probing the metal carbonyl and organic carbonyl vibrations of the one-electron-reduced forms of two Re-based CO2 reduction catalysts in acetonitrile solution. Transient IR absorption bands with amplitudes on the order of 1 × 10−3 are easily detected on the sub-microsecond timescale using electron pulses as short as 250 ns.

Primary radiolytic species such as the solvated electron (es–) and Cl2•– are key to predicting radiation effects on the long-term behavior of molten salt reactor fuel.

To examine ion solvation, exchange, and speciation for minority components in molten salts (MS) typically found as corrosion products, we propose a multimodal approach combining extended X-ray absorption fine structure (EXAFS) spectroscopy, optical spectroscopy, ab initio molecular dynamics (AIMD) simulations, and rate theory of ion exchange. Going beyond conventional EXAFS analysis, our method can accurately quantify populations of different coordination states of ions with highly disordered coordination environments via linear combination fitting of the EXAFS spectra of these coordination states computed from AIMD to the experimental EXAFS spectrum. In a case study of dilute Ni(II) dissolved in the ZnCl2+KCl melts, our method reveals heterogeneous distributions of coordination states of Ni(II) that are sensitive to variations in temperature and melt composition. These results are fully explained by the difference in the chloride exchange dynamics at varied temperatures and melt compositions. This insight will enable a better understanding and control of ion solubility and transport in MS.

Room temperature post-irradiation measurements of diffuse reflectance and electron paramagnetic resonance spectroscopies were made to characterize the long-lived radiation-induced species formed from the gamma irradiation of solid KCl, MgCl2, and ZnCl2 salts up to 100 kGy. The method used showed results consistent with those reported for electron and gamma irradiation of KCl in single crystals. Thermal bleaching of irradiated KCl demonstrated accelerated disaggregation of defect clusters above 400 K, due to decomposition of Cl3−. The defects formed in irradiated MgCl2 comprised a mixture of Cl3−, F-centers, and Mg+ associated as M-centers. Further, Mg metal cluster formation was also observed at 100 kGy, in addition to accelerated destruction of F-centers above 20 kGy. Irradiated ZnCl2 afforded the formation of Cl2− due to its high ionization potential and crystalline structure, which decreases recombination. The presence of aggregates in all cases indicates the high diffusion of radicals and the predominance of secondary processes at 295 K. Thermal bleaching studies showed that chloride aggregates’ stability increases with the ionization potential of the cation present. The characterization of long-lived radiolytic transients of pure salts provides important information for the understanding of complex salt mixtures under the action of gamma radiation.

Knowledge of structural and thermal properties of molten salts is crucial for understanding and predicting their stability in many applications such as thermal energy storage and nuclear energy systems. Probing the behavior of metal contaminants in molten salts is presently limited to either foreign ionic species or metal nanocrystals added to the melt. To bridge the gap between these two end states and follow the nucleation and growth of metal species in molten salt environment in situ, we use synchrotron X-rays as both a source of solvated electrons for reducing Ni2+ ions added to ZnCl2 melt and as an atomic-level probe for detecting formation of zerovalent Ni nanoparticles. By combining extended X-ray absorption fine structure analysis with X-ray absorption near edge structure modeling, we obtained the average size and structure of the nanoparticles and proposed a radiation-induced reduction mechanism of metal ions in molten salts.

Understanding the factors that control solubility and speciation of metal ions in molten salts is key for their successful use in molten salt reactors and electrorefining. Here, we employ X-ray and...

In the past 15 years, magic angle spinning (MAS) dynamic nuclear polarization (DNP) has emerged as a method to increase the sensitivity of high-resolution solid-state NMR spectroscopy experiments. Recently, γ-irradiation has been used to generate significant concentrations of homogeneously distributed free radicals in a variety of solids, including quartz, glucose, and cellulose. Both γ-irradiated quartz and glucose previously showed significant MAS DNP enhancements. Here, γ-irradiation is applied to twelve small organic molecules to test the applicability of γ-irradiation as a general method of creating stable free radicals for MAS DNP experiments on organic solids and pharmaceuticals. Radical concentrations in the range of 0.25 ​mM-10 ​mM were observed in irradiated glucose, histidine, malic acid, and malonic acid, and significant

Molten salts are proposed as liquid fuels or coolants in a new fleet of molten salt nuclear reactors that would have operational and safety advantages over present reactor systems. Under those conditions, the salt will be exposed to high radiation levels, and understanding the chemical effects of radiolysis on the molten salt fuel or coolant is essential to reliable, efficient and sustainable reactor operation. Building this understanding begins with identifying primary salt radiolysis products and characterizing their reactivities, for which we perform high-temperature pulse radiolysis transient absorption spectroscopy at the BNL Laser-Electron Accelerator Facility. Salt mixtures containing monovalent and divalent cations are of particular interest because of their tunable Lewis acidity-basicity that can be used to control the solubility of dissolved metal ions in the reactor. Changing the MgCl2:KCl mixing ratio alters the absorption spectra of radiolytically-produced excess electrons, with increasing blue shifts related to the probable number of Mg2+ ions close to the cavity electron. These strong blue shifts imply significant changes in the electron’s energetics and reactivity that we quantify by measuring reaction kinetics with metal ion electron acceptors. This work was supported as part of the Molten Salts in Extreme Environments Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science.

In the present work, the electrochemical corrosion tests were performed on single-crystal nickel and chromium with different surface orientations having (100), (110), and (111) facets, in a MgCl2-KCl eutectic molten salt at 500oC under an argon atmosphere. The corrosion rate of Ni is lower than that of Cr, indicating that Ni is electrochemically more stable than Cr in the molten salt. The anodic corrosion rates of different single crystals increase in the order of (111) < (100) < (110). This observation shows that the degree of electrochemical stability is related to the coordination of surface atoms and lower density surfaces yield higher corrosion rates. In addition, the corrosion rate of a polycrystalline sample is similar to that of the single-crystal (110) sample, which suggests that the corrosion rate of the polycrystalline surface is dominated by the orientation with the lowest surface density. This work was supported as part of the Molten Salts in Extreme Environments Energy Frontier Research Center, funded by the U.S. Department of Energy, Office of Science. Keywords: Tafel, Nickel, Chromium, MgCl2-KCl, Single crystal.

The use of molten salts for large-scale solar concentrated power plants and molten salt reactors has been driving the research to better understand how metals and alloys interact with the molten salt. As the metals may undergo morphological, chemical, and structural change in molten salt environments, it is critical to understand the fundamental mechanisms in these changes. In this work, we will present how we utilized synchrotron X-ray nano-tomography to better understand the 3D morphological evolution of Ni, Cr, and their alloys in molten salt. The effects of temperature and additives in the salt on the morphological evolution will be discussed. At the higher temperature, a characteristic bicontinuous structure can form from molten salt dealloying a binary alloy. [1] This contrasts to the intergranular corrosion found in the same system reacted at a lower temperature. [2] Different additives in the salt were also found to alter the morphological changes of the alloys and can create planar corrosion, percolation dealloying, or redeposition. To complement the morphological studies by X-ray nano-tomography, a suite of X-ray and electron microscopy analyses were also carried out to better understand the chemical and structural (both short-and long-range ordering) evolution. Taking it as a multimodal approach, we will discuss how we couple the analysis from synchrotron operando X-ray absorption spectroscopy, diffraction, and imaging, as well as the multiscale imaging studies from both X-ray and electron microscopy. This work was supported as part of the Molten Salts in Extreme Environments (MSEE) Energy Frontier Research Center (EFRC), funded by the U.S. Department of Energy, Office of Science. References: [1] "Formation of three-dimensional bicontinuous structures via molten salt dealloying studied in real-time by in situ synchrotron X-ray nano-tomography" Xiaoyang Liu, Arthur Ronne*, Lin-Chieh Yu, Yang Liu, Mingyuan Ge, Cheng-Hung Lin, Bobby Layne, Phillip Halstenberg, Dmitry S. Maltsev, Alexander S. Ivanov, Stephen Antonelli, Sheng Dai, Wah-Keat Lee, Shannon M. Mahurin, Anatoly I. Frenkel, James F. Wishart, Xianghui Xiao & Yu-chen Karen Chen-Wiegart* Nature Communications (2021), DOI: 10.1038/s41467-021-23598-8 [2] "Visualizing time-dependent microstructural and chemical evolution during molten salt corrosion of Ni-20Cr model alloy using correlative quasi in situ TEM and in situ synchrotron X-ray nano-tomography" Kaustubh Bawane, Xiaoyang Liu, Ruchi Gakhar, Michael Woods, Mingyuan Ge, Xianghui Xiao, Wah-Keat Lee, Philip Halstenberg, Sheng Dai, Shannon Mahurin, Simon M. Pimblott, James F. Wishart, Yu-chen Karen Chen-Wiegart*, Lingfeng He* Corrosion Science (2021), DOI: 10.1016/j.corsci.2021.109962

Three-dimensional bicontinuous porous materials formed by dealloying contribute significantly to various applications including catalysis, sensor development and energy storage. This work studies a method of molten salt dealloying via real-time in situ synchrotron three-dimensional X-ray nano-tomography. Quantification of morphological parameters determined that long-range diffusion is the rate-determining step for the dealloying process. The subsequent coarsening rate was primarily surface diffusion controlled, with Rayleigh instability leading to ligament pinch-off and creating isolated bubbles in ligaments, while bulk diffusion leads to a slight densification. Chemical environments characterized by X-ray absorption near edge structure spectroscopic imaging show that molten salt dealloying prevents surface oxidation of the metal. In this work, gaining a fundamental mechanistic understanding of the molten salt dealloying process in forming porous structures provides a nontoxic, tunable dealloying technique and has important implications for molten salt corrosion processes, which is one of the major challenges in molten salt reactors and concentrated solar power plants., Understanding how pores evolve in metals submerged in molten salts is important for nanofabrication technology and molten salt corrosion in nuclear and solar power plants. Here, the authors present an in situ X-ray 3D imaging to directly visualize and quantify the process.

High-field magic angle spinning dynamic nuclear polarization (MAS DNP) is often used to enhance the sensitivity of solid-state nuclear magnetic resonance experiments by transferring spin polarization from electron spins to nuclear spins. Here, we demonstrate that γ-irradiation induces the formation of stable radicals in inorganic solids, such as fused quartz and borosilicate glasses, as well as organic solids, such as glucose, cellulose, and a urea/polyethylene polymer. The radicals were then used to polarize 29Si or 1H spins in the core of some of these materials. Significant MAS DNP enhancements (e) of more than 400 and 30 were obtained for fused quartz and glucose, respectively. For other samples, negligible values of e were obtained, likely due to low concentrations of radicals or the presence of abundant quadrupolar spins. These results demonstrate that ionizing radiation is a promising alternative method for generating stable radicals that are suitable for high-field MAS DNP experiments.

Room temperature post-irradiation measurements of diffuse reflectance and electron paramagnetic resonance spectroscopies were made to characterize the long-lived radiation-induced species formed from the gamma irradiation of solid KCl, MgCl2, and ZnCl2 salts up to 100 kGy. The method used showed results consistent with those reported for electron and gamma irradiation of KCl in single crystals. Thermal bleaching of irradiated KCl demonstrated accelerated disaggregation of defect clusters above 400 K, due to decomposition of Cl3-. The defects formed in irradiated MgCl2 comprised a mixture of Cl3-, F-centers, and Mg+ associated as M-centers. Further, Mg metal cluster formation was also observed at 100 kGy, in addition to accelerated destruction of F-centers above 20 kGy. Irradiated ZnCl2 afforded the formation of Cl2- due to its high ionization potential and crystalline structure, which decreases recombination. The presence of aggregates in all cases indicates the high diffusion of radicals and the predominance of secondary processes at 295 K. Thermal bleaching studies showed that chloride aggregates' stability increases with the ionization potential of the cation present. The characterization of long-lived radiolytic transients of pure salts provides important information for the understanding of complex salt mixtures under the action of gamma radiation.

Super-concentrated "water-in-salt" electrolytes recently spurred resurgent interest for high energy density aqueous lithium-ion batteries. Thermodynamic stabilization at high concentrations and kinetic barriers towards interfacial water electrolysis significantly expand the electrochemical stability window, facilitating high voltage aqueous cells. Herein we investigated LiTFSI/H2O electrolyte interfacial decomposition pathways in the "water-in-salt" and "salt-in-water" regimes using synchrotron X-rays, which produce electrons at the solid/electrolyte interface to mimic reductive environments, and simultaneously probe the structure of surface films using X-ray diffraction. We observed the surface-reduction of TFSI(-)at super-concentration, leading to lithium fluoride interphase formation, while precipitation of the lithium hydroxide was not observed. The mechanism behind this photoelectron-induced reduction was revealed to be concentration-dependent interfacial chemistry that only occurs among closely contact ion-pairs, which constitutes the rationale behind the "water-in-salt" concept., Angewandte Chemie. International Edition, 59 (51), ISSN:1433-7851, ISSN:1521-3773, ISSN:0570-0833

To facilitate the development of molten salt reactor technologies, a fundamental understanding of the physical and chemical properties of molten salts under the combined conditions of high temperature and intense radiation fields is necessary. Optical spectroscopic (UV-Vis-near IR) and electrochemical techniques are powerful analytical tools to probe molecular structure, speciation, thermodynamics, and kinetics of solution dynamics. Here, we report the design and fabrication of three custom-made apparatus: (i) a multi-port spectroelectrochemical furnace equipped with optical spectroscopic and electrochemical instrumentation, (ii) a high-temperature cell holder for time-resolved optical detection of radiolytic transients in molten salts, and (iii) a miniaturized spectroscopy furnace for the investigation of steady-state electron beam effects on molten salt speciation and composition by optical spectroscopy. Initial results obtained with the spectroelectrochemical furnace (i) and high-temperature cell holder (ii) are reported.

A versatile, compact heater designed at National Synchrotron Light Source-II forin situX-ray nano-imaging in a full-field transmission X-ray microscope is presented. Heater design for nano-imaging is challenging, combining tight spatial constraints with stringent design requirements for the temperature range and stability. Finite-element modeling and analytical calculations were used to determine the heater design parameters. Performance tests demonstrated reliable and stable performance, including maintaining the exterior casing close to room temperature while the heater is operating at above 1100°C, a homogenous heating zone and small temperature fluctuations. Two scientific experiments are presented to demonstrate the heater capabilities: (i)in situ3D nano-tomography including a study of metal dealloying in a liquid molten salt extreme environment, and (ii) a study of pore formation in icosahedral quasicrystals. The progression of structural changes in both studies were clearly resolved in 3D, showing that the new heater enables powerful capabilities to directly visualize and quantify 3D morphological evolution of materials under real conditions by X-ray nano-imaging at elevated temperature during synthesis, fabrication and operation processes. This heater design concept can be applied to other applications where a precise, compact heater design is required.

Understanding the factors that control solubility and speciation of metal ions in molten salts is key for their successful use in molten salt reactors and electrorefining. Here, we employ X-ray and optical absorption spectroscopies and molecular dynamics simulations to investigate the coordination environment of Ni(II) in molten ZnCl

In situ monitoring of corrosion processes is important to fundamentally understand the kinetics and evolution of materials in harsh environments. A quasi in situ transmission electron microscopy technique was utilized to study microstructural and chemical evolution of a Ni-20Cr disc sample exposed to molten KCl-MgCl2 salt for 60 s in consecutive 20 s iterations. In situ synchrotron X-ray nanotomography was performed to characterize the morphological evolution of a Ni-20Cr microwire exposed to molten KCl-MgCl2. Both techniques captured key corrosion events and revealed mechanisms at different time and length scales, potentially bringing greater insights and deeper understanding beyond conventional analysis.

A pulse radiolysis study on pyrrolidinium cation based ionic liquids is presented herein. Time-resolved absorption spectra for 1-methyl-1-propylpyrrolidinium dicyanamide (DCA) at 500 ns after the electron pulse show broad absorption bands at wavelengths below 440 nm and at 640 nm. In pyrrolidinium bis(trifluoromethylsulfonyl)imide (NTf2) and tris(perfluoroethyl)trifluorophosphate (FAP) ILs, the transient absorption below 440 nm is much weaker. The absorption at 500 ns, which increases with wavelength from 500 nm to beyond 800 nm, was assigned to the tail of the solvated electron NIR absorption spectrum, since it disappears in the presence of N2O. In the DCA IL, the presence of a reducing species was confirmed by the formation of pyrene radical anion. The difference in the transient species in the case of the DCA IL compared to other two ILs should be due to the anion, with cations being similar. In pseudohalide ILs such as DCA, radicals are formed by direct hole trapping by the anion (X– + h+ → X•), follo...

This work utilizes electron energy loss spectroscopy (EELS) to identify oxidation state of alloying elements in Ni-based alloys after exposure to molten chloride salt systems. Pure Ni and Ni-20Cr model alloy were corroded in molten ZnCl2 and KCl-MgCl2 under argon atmosphere at various temperatures. Oxidation states of Cr (Cr3+) and Ni (Ni2+) in the molten salt after corrosion were determined by monitoring changes in the L2,3 edges of corresponding EELS spectra. Oxidation state mapping technique using principal component analysis and multiple linear least squares fitting in HyperSpy Python package was developed.

Corrosion of Ni and Ni-20Cr in molten ZnCl2 under argon atmosphere at 593 K was investigated using cyclic polarization in combination with various electron microscopy techniques. Cyclic polarization measurements yielded significantly lower corrosion rates for pure Ni than for Ni-20Cr. Corrosion of the Ni-20Cr alloy is attributed to selective anodic dissolution of Cr, which forms a chromium chloride film at the metal-salt interface. The corrosion in Ni and Ni-20Cr is accelerated by grain boundary attack through intergranular corrosion, followed by the formation of pore-salt network regions. The related corrosion mechanisms and dissolution kinetics are discussed.

Solvent based extractions of used nuclear fuel use designer ligands in an organic phase extracting ligand complexed metal ions from an acidic aqueous phase. These extractions will be performed in highly radioactive environments, and the radiation chemistry of all these complexants and their diluents will play a major role in determining extraction efficiency, separation factors, and solvent-recycle longevity. Although there has been considerable effort in investigating ligand damage occurring in acidic water radiolysis conditions, only minimal fundamental kinetic and mechanistic data has been reported for the degradation of extraction ligands in the organic phase. Extraction solvent phases typically use normal alkanes such as dodecane, TPH, and kerosene as diluents. The radiolysis of such diluents produce a mixture of radical cations (R•+), carbon-centered radicals (R•), solvated electrons, and molecular products such as hydrogen. Typically, the radical species will preferentially react with the dissolved oxygen present to produce relatively inert peroxyl radicals. This isolates the alkane radical cation species, R•+ as the major radiolytically-induced organic species that can react with, and degrade, extraction agents in this phase. Here we report on our recent studies of organic radical cation reactions with various ligands. Elucidating these parameters, and combining them with the known acidic aqueous phase chemistry, will allow a full, fundamental, understanding of the impact of radiation on solvent extraction based separation processes to be achieved.

The photochemistry of the charge transfer (CT) band of the room temperature ionic liquid (RTIL) 1-hexyl-3-methylimidazolium bromide (HMIm + /Br − ) is investigated using near-IR to vis ultrafast transient absorption (TA) and steady-state UV absorption spectroscopies. Continuous irradiation of the CT band at 266 nm results in the formation of photo-products that absorb strongly at 266 nm. It is shown that these photo-products, which are apparently very stable, adversely affect ultrafast TA measurements. Elimination of these effects reveals at least two transient species that exist within the TA detection window of 100 fs to 3 ns and 500–1250 nm. One of the components is a short-lived (

A thorough understanding of radiation effects on molten salt media is necessary to support the design, development, and deployment of molten salt reactor, using either fuel salt or solid fuel with salt as the coolant. Fundamental issues include the determination of the initial yields and reactivity of the primary radiolytic species, i.e., the solvated electron (esolv –), chlorine atom (Cl•), and dichloride radical anion (Cl2 •–) as their reactivity varies depending on the environment such as the salt cation and temperature. Here we report on the reaction kinetics for esolv – and Cl2 •– in molten LiCl-KCl eutectic doped with Zn2+ ions. Electron pulse radiolysis absorption spectroscopy was used to observe the transient behavior of esolv – and Cl2 •– on the nanosecond to microsecond time scale. Experiments were performed using the Brookhaven National Laboratory Laser-Electron Accelerator Facility (LEAF)1 and utilizing a recently developed high-temperature sample holder.2 Decay kinetics of of esolv – and Cl2 •– in 9.41 mM ZnCl2 in LiCl-KCl are shown in the figure. esolv – and Cl2 •– decays in different time scale due to different reaction kinetics and decay speed increase as temperature. This work was supported as part of the Molten Salts in Extreme Environments Energy Frontier Research Center, funded by the U.S. Department of Energy (US-DOE), Office of Science, Basic Energy Sciences, at BNL, INL and ORNL under contracts DE-SC0012704, DE-AC07-05ID14517 and DE-FC02-04ER15533, respectively. The Laser Electron Accelerator Facility of the BNL Accelerator Center for Energy Research is supported by the US-DOE Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences under contract DE-SC0012704. Wishart, J. F.; Cook, A. R.; Miller, J. R.; Rev. Sci. Instrum., 2004, 75 (11), 4359. Phillips, W. C.; Layne, B.; Gakhar, R.; Horne, G. P.; Ramos-Ballesteros, A.; Iwamatsu, K.; LaVerne, J. A.; Pimblott, S. M.; Wishart, J. F.; Rev. Sci. Instrum., 2019, in peer review. Figure 1

Molten Salt Reactors (MSRs) are a potential game-changing technology for next-generation nuclear power. Although the MSR concept was demonstrated at Oak Ridge National Laboratory (ORNL) in the 1960’s, it had not gathered attention from commercial vendors until recently. A fundamental knowledge of salt chemistry, including the speciation and solubility of corrosion and fission products is central to the safe and reliable operation of MSRs. The structural properties of fused salt solutions, especially the coordination geometry around the metal ions in the melt, are intricately dependent on the melt composition and temperature. In this work, a combination of in-situ electrochemistry and optical absorption spectroscopy techniques are utilized to understand the speciation and structure of lanthanides in molten chloride salts as a function of temperature, concentration and melt composition. The spectroelectrochemistry of metal species in molten salt media can be used as a potential process monitoring technique enabling the quantitative measurement of lanthanide and actinide metals within molten salt reactors or nuclear fuel pyro-processing applications. This work was supported as part of the Molten Salts in Extreme Environments Energy Frontier Research Center, funded by the U.S. Department of Energy (US-DOE), Office of Science, Basic Energy Sciences, at BNL, INL and ORNL under contracts DE-SC0012704, DE-AC07-05ID14517 and DE-FC02-04ER15533, respectively.

Molten Salt Reactors (MSRs) are the leading candidates out of the six-generation IV advanced nuclear power reactor designs chosen for deployment for nuclear energy in US. MSR technology is particularly attractive due to better passive safety, operation at atmospheric pressure, high thermal efficiency, lower spent fuel per unit energy and increased solubility of fission products in molten salts. To facilitate robust and economical design of such systems, accurate knowledge and fundamental understanding of the structure and speciation of salts and metals in and near molten salt environments is necessary. Speciation of solutes is important because it determines how chemical behavior in solution and complex speciation from fission and corrosion products impact kinetic, thermodynamic, and transport properties of the molten salt systems. Investigating effects of radiation on metallic species and radiation-induced nucleation and growth of metallic nanoparticles under ionizing radiation is crucial for predicting the stability and reactivity of molten salts. Molten Salts in Extreme Environments (MSEE) EFRC aims to investigate speciation of metals and radiation-induced reactions in molten salt systems by utilizing synchrotron based XAS methods. In our work, Extended X-ray Absorption Fine Structure (EXAFS) and X-Ray Absorption Near Edge structure (XANES) are used to investigate local coordination environment and chemical structure of metal species such as Nickel in Zinc Chloride based molten salt systems. In addition, the effect of metal concentration and temperature on changes in local and chemical structure of metal is studied. XAS studies are complemented by optical ultra-violet spectroscopy studies of molten salts, enabling a direct correspondence between UV-Vis peak shape and coordination geometry and number, determined by EXAFS. Such knowledge of speciation of metals and radiation-induced nanoparticles in molten salt environments will provide critical understanding needed to predict and control the physical and chemical properties of molten salts and corrosion mechanisms in molten salt systems. This work was supported as part of the Molten Salts in Extreme Environments, Energy Frontier Research Center, funded by the U.S. Department of Energy Office of Science.

Mixtures of ionic liquids (ILs) containing single-walled carbon nanotubes (SWCNTs) were prepared and characterized to obtain electrolytes with optimized transport properties for the use in energy storage devices such as supercapacitors. Imidazolium ILs bearing cations with side chains of different functionality coupled with bis(trifluoromethylsulfonyl)amide (NTf2 -) or bis(fluorosulfonyl)amide (FSA-) anions were used in mixtures containing up to 5 wt % SWCNTs. It was determined that the ionic conductivities of all ILs studied can be significantly increased with the addition of single-walled carbon nanotubes when the loading of the nanotubes is above 2 wt %. Moreover, higher conductivities were observed for the ILs containing the NTf2 - anion and 5 wt % SWCNTs. These results can significantly contribute to the development of improved energy storage devices. The work at Brookhaven National Laboratory was supported by the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences under contract DE-SC0012704. The work at Brooklyn College was supported by the National Science Foundation, Solid State and Materials Chemistry Program, Division of Materials Research, EAGER award #1841398.

Molten chloride and fluoride salts possess various properties such as good thermal conductivity and stability, large specific heat and low viscosity which make them important as fuels and/or coolants for molten salt reactors (MSR). Molten chloride salts are also selected as heat transfer and storage fluids to carry thermal energy from a solar concentrator to a steam generator in concentrating solar power (CSP) technologies. In both the applications the nickel-based alloys are used as structural materials. However high operating temperatures and extremely corrosive nature of molten salts promote faster corrosion of the structural materials. Hence, the corrosion behavior of the structural materials needs to be understood and monitored with time when exposed to the corrosive molten salt environment. Electrochemical techniques are useful for understanding the corrosion mechanism of metals and alloys in molten salts. Among them, electrochemical noise (ECN) is a simple in-situ technique to monitor the corrosion in real time without applying any external signals to the metal/alloy in corrosive environments. A unique advantage of ECN technique is the possibility to detect and analyze the early stages of the localized corrosion process during corrosion initiation as well as a type of corrosion. The corrosion of metals and alloys in molten chloride is strongly affected by impurities (O2, H2O) present in the atmosphere, temperature changes, and concentrations of various chemical impurities (metal oxides and metal chlorides). These impurities have been considered as strong oxidizing agents for metals and alloys in molten chloride salts. Chromium is a major alloying element in nickel-based alloys. Cr can be oxidized into metal chlorides CrClx (x=2,3) due to their favorable Gibbs free energies of the formation as compared to NiCl2 at 623 K. Cr3+ and Cr2+ coexist in the molten salt during corrosion of nickel-based alloys, while Cr3+ is the primary valence state. It is important to study the effect of these multi-valent ions on corrosion of metals/alloys in molten salts. To the best of our knowledge, no study on the effect of Cr3+ on the metals/alloys in molten chloride medium has been reported. The effect of CrCl3 on the corrosion behaviour of Ni and Ni-20 wt %Cr (NiCr) alloy in purified molten ZnCl2 at 623 K was investigated for the first time using ECN measurements in an argon-filled glovebox. ECN measurements were carried out in a three-electrode setup using two working electrodes and platinum as a reference electrode in molten CrCl3-ZnCl2 at 623 K. Ni and NiCr corrosion behavior was examined in two different combinations : 1) identically coupled electrodes (Ni-Ni and NiCr-NiCr vs Pt) and 2) galvanically coupled electrodes (Ni-NiCr vs Pt). Different types of current and potential noise fluctuations have been identified for pitting and other forms of corrosion. Analysis of fluctuations in current and potential noise in Ni and NiCr in all the three combinations concluded that Ni and NiCr exhibited localized corrosion. The addition of CrCl3 to ZnCl2 accelerated the dissolution of Cr and Ni at the metal-salt interface. After ECN studies, the working electrodes were examined by scanning transmission electron microscopy (STEM) coupled with energy dispersive X-ray spectroscopy (EDS) and electron energy loss spectroscopy (EELS). STEM/EDS/EELS observations confirmed pit formation, Ni and Cr dissolution, and Cr depletion at the salt-metal interfaces. Ni-rich and Cr-depleted precipitates were observed in the salt with a galvanically coupled NiCr electrode after ECN studies. The in-depth ECN results will be discussed in conjunction with micro- and nano-scale imaging of dissolution of Ni and Cr elements at the metal-salt interface, and plausible corrosion mechanisms will be proposed. The present ECN results on Ni and NiCr are compared with ECN studies in pure ZnCl2 salt. This work was supported as part of the Molten Salts in Extreme Environments Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science.

A variety of molten salts are proposed as liquid fuels or coolants in a new fleet of molten salt nuclear reactors that would have operational and safety advantages over present reactor systems. The molten salt will be exposed to high radiation levels under these conditions, therefore understanding the chemical effects of radiolysis on the molten salt fuel or coolant is essential to reliable, efficient and sustainable reactor operation. This understanding begins with identifying the primary salt radiolysis products and characterizing their reactivities, in pure salt and also under conditions that represent loading with fuel (actinides), fission products and corrosion products. These reactions form subsequent products that determine the chemical evolution of the molten salt fuel over the duration of its lifetime in the reactor. To obtain predictive insight into this radiation-driven chemical evolution, we investigate these reactions by performing pulse radiolysis transient absorption spectroscopy at the BNL Laser-Electron Accelerator Facility using a high-temperature sample configuration. Examples will be given of how the composition of the molten salt determines the identities and reactivities of the primary radiolysis products, and we will follow their reactions with metal ions that are representative of the reactor fuel environment. This work was supported as part of the Molten Salts in Extreme Environments Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science. Figure 1

In this study, we investigate the temperature dependence of low-frequency spectra in the frequency range of 0.3–200 cm−1 for ionic liquids (ILs) whose cations possess two systematically different cyclic groups, using femtosecond Raman-induced Kerr effect spectroscopy. The target ILs are bis(trifluoromethylsulfonyl)amide [NTf2]– salts of 1-cyclohexylmethyl-1-methylpyrrolidinium [CHxmMPyrr]+, 1-cyclohexylmethyl-3-methylimidazolium [CHxmMIm]+, N-cyclohexylmethylpyridinium [CHxmPy]+, 1-benzyl-1-methylpyrrolidinium [BzMPyrr]+, 1-benzyl-3-methylimidazolium [BzMIm]+, and N-benzylpyridinium [BzPy]+ cations. The aim of this study is to better understand the effects of aromaticity in the cations’ constituent groups on the temperature-dependent low-frequency spectral features of the ILs. The low-frequency spectra of these ILs are temperature dependent, but the temperature-dependent spectrum of [CHxmMPyrr][NTf2] is different from that of other ILs. While [CHxmMPyrr][NTf2] shows spectral changes with temperature in th...

A comprehensive variable temperature, pressure and frequency multinuclear (1H, 2H, and 19F) magnetic resonance study was undertaken on selectively deuterated 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide (BMIM TFSA) ionic liquid isotopologues. This study builds on our earlier investigation of the effects of increasing alkyl chain length on diffusion and dynamics in imidazolium-based TFSA ionic liquids. Fast field cycling 1H T1 data revealed multiple modes of motion. Through calculation of diffusion coefficient (D) values and activation energies, the low- and high-field regimes were assigned to the translational and reorientation dynamics respectively. Variable-pressure 2H T1 measurements reveal site-dependent interactions in the cation with strengths in the order MD3 > CD3 > CD2, indicating dissimilarities in the electric field gradients along the alkyl chain, with the CD2 sites having the largest gradient. Additionally, the α saturation effect in T1 vs. P was observed for all three sites, suggesting significant reduction of the short-range rapid reorientational dynamics. This reduction was also deduced from the variable pressure 1H T1 data, which showed an approach to saturation for both the methyl and butyl group terminal methyl sites. Pressure-dependent D measurements show independent motions for both cations and anions, with the cations having greater D values over the entire pressure range.

International audience

International audience

Multinuclear ((1)H, (2)H, and (19)F) magnetic resonance spectroscopy techniques as functions of temperature and pressure were applied to the study of selectively deuterated 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide (EMIM TFSA) ionic liquid isotopologues and related ionic liquids. For EMIM TFSA, temperature-dependent (2)H T1 data indicate stronger electric field gradients in the alkyl chain region compared to the imidazolium ring. Most significantly, the pressure dependences of the EMIM and TFSA self-diffusion coefficients revealed that the displacements of the cations and anions are independent, with diffusion of the TFSA anions being slowed much more by increasing pressure than for the EMIM cations, as shown by their respective activation volumes (28.8 ± 2.5 cm(3)/mol for TFSA vs 14.6 ± 1.3 cm(3)/mol for EMIM). Increasing pressure may lower the mobility of the TFSA anion by hindering its interconversion between trans and cis conformers, a process that is coupled to diffusion according to published molecular dynamics simulations. Measured activation volumes (ΔV(‡)) for ion self-diffusion in EMIM bis(fluoromethylsulfonyl)amide and EMIM tetrafluoroborate support this hypothesis. In addition, (2)H T1 data suggest increased ordering with increasing pressure, with two T1 regimes observed for the MD3 and D2 isotopologues between 0.1-100 and 100-250 MPa, respectively. The activation volumes for T1 were 21 and 25 cm(3)/mol (0-100 MPa) and 11 and 12 cm(3)/mol (100-250 MPa) for the MD3 and D2 isotopologues, respectively.

The dodecane radical cation reaction rate constant with CMPO was measured using ps electron pulse radiolysis/absorption spectroscopy as k = (1.30 ± 0.11) × 1010 M−1s−1 in dodecane/0.10 M CH2Cl2 solution. No reactivity increase occurred when these solutions were pre-contacted with nitric acid, similar to the behavior observed for TODGA. To corroborate these kinetic data with steady-state radiolysis measurements, where acid pre-contacted CMPO showed significantly less degradation, it is proposed that the dodecane radical cation always reacts directly with TODGA, but for CMPO the charge-transfer occurs with the CMPO·HNO3 complex formed in the acid contacted solvent.

Rechargeable lithium-ion batteries containing silicon-based negative electrodes have the potential to revolutionize electrical energy storage, but the cyclic and acyclic organic carbonate solvents (such as ethylene and propylene carbonates) that are commonly used in graphite Li-ion batteries yield unsatisfactory performance when used with such Li alloying electrodes. It has been found by trial and error that additions of the closely related carbonate additive, fluoroethylene carbonate (FEC), to conventional electrolytes yields a robust solid electrolyte interphase (SEI) on the LixSiy alloy surface. Several mechanisms for this protective action have been considered in the literature and modeled theoretically; however, at present these mechanisms remain hypothetical. In this study, we use radiolysis, laser photoionization, electron paramagnetic resonance, and transient absorption spectroscopy to establish the redox chemistry of FEC. While the oxidation chemistry is similar to that of other organic carbonate...

We report the synthesis, characterization and cellulose dissolution properties of a series of ionic liquids bearing alkyl and hydroxyl-functionalized imidazolium and pyrrolidinium cations, and dial...

Solutions of TODGA and T(EH)DGA in n-dodecane were subjected to γ-irradiation in the presence and absence of an aqueous nitric acid phase and analyzed using UHPLC-ESI-MS to determine the rates of radiolytic decay of the two extractants, as well as to identify radiolysis products. The DGA concentrations decreased exponentially with increasing dose, and the measured degradation rate constants were uninfluenced by the presence or absence of an acidic aqueous phase, or by chemical variations in the alkyl side-chains. The DGA degradation was attributed to reactions of the dodecane radical cation, whose kinetics were measured for TODGA using picosecond electron pulse radiolysis to be k2 = (9.72 ± 1.10) × 109 M−1 s−1. The identified radiolysis products suggest that the bonds most vulnerable to radiolytic attack are those in the diglycolamide center of these molecules and not on the side-chains.