ABSTRACT
In this study, we demonstrate that elastic strain applied to a current collector can influence the overall thermodynamic and kinetic picture of sodium metal electrodeposition and hence the performance of a sodium metal battery. To controllably study the role of strain in electrochemical performance, we utilize NiTi foil as a stable current collector, nucleation interface, and superelastic material. Our findings demonstrate that a locked-in elastic tensile strain near 8% results in 40 mV lower onset potential for sodium electrodeposition, 19% decrease in charge transfer resistance, and 20% lower cumulative sodium loss, among other effects. These performance improvements are correlated primarily to the control of the irreversible behavior in the first few minutes of electroplating. Given the prevalence of strain buildup in commercial battery cell configurations, our work highlights that strained current collector interfaces can result in significant long-term chemo-mechanical performance outcomes broadly relevant to sodium and other metal battery design considerations.
ABSTRACT
Dynamic tuning of metamaterials is a critical step toward advanced functionality and improved bandwidth. In the visible spectrum, full spectral color tuning is inhibited by the large absorption that accompanies index changes, particularly at blue wavelengths. Here, we show that the electrochemical lithiation of anatase TiO2 to Li0.5TiO2 (LTO) results in an index change of 0.65 at 649 nm with absorption coefficient less than 0.1 at blue wavelengths, making this material well-suited for dynamic visible color tuning. Dynamic tunability of TiO2 is leveraged in a Fabry-Perot cavity and a gap plasmon metasurface. In the Fabry-Perot configuration, the device exhibits a shift in reflectance of over 100 nm when subjected to only 2 V bias while the gap plasmon metasurface achieves enhanced switching speed. The dynamic range, speed, and cyclability indicate that the TiO2/LTO system is competitive with established actuators like WO3, with the additional advantage of reduced absorption at high frequencies.
ABSTRACT
This effort demonstrates the development of a novel, graphene oxide nanoscale thermite composite with thermally tunable microwave ignitability. A model thermite system containing nanoscale aluminum and nanoscale iron(II) oxide in a stoichiometric ratio (30/70 wt %) was combined with sheets of graphene oxide (GO) or reduced graphene oxide (rGO) using an immiscible two-fluid sonication and tape casting process. The samples were microwave irradiated within a single-mode resonant microwave cavity to determine the microwave ignition delay. Neat thermites were found to ignite after 4.34 s of microwave illumination, whereas 30 wt % rGO thermite composite ignition delay was an order of magnitude shorter (0.43 s). For most samples (4 of 6 trials), it was found that application of a 30 wt % GO coating inhibits microwave ignition of the thermite. Thermal treatment of the GO thermite composite led to switching of thermites from unignitable to ignitable with microwave field application as short as 0.24 s due to GO reduction. Optimum heat treatment time and GO content are explored with SEM, DSC/TGA-MS, Raman, and XPS deconvolution. This effort demonstrates the use of GO and rGO addition to achieve thermally switchable microwave ignitability to electromagnetically shield or enhance nanoscale energetic ignition by microwave energy.
ABSTRACT
Layered two-dimensional (2D) black phosphorus (BP) exhibits novel semiconducting properties including a tunable bandgap and high electron mobility. However, the poor stability of BP in ambient environment severely limits potential for application in future electronic and optoelectronic devices. While passivation or encapsulation of BP using inert materials/polymers has emerged as a plausible solution, a detailed fundamental understanding of BP's reaction with oxygen is imperative to rationally advance its use in applications. Here, we use in situ environmental transmission electron microscopy to elucidate atomistic structural changes in mechanically exfoliated few-layered BP during exposure to varying partial pressures of oxygen. An amorphous oxide layer is seen on the actively etching BP edges, and the thickness of this layer increases with increasing oxygen partial pressure, indicating that oxidation proceeds via initial formation of amorphous PxOy species which sublime to result in the etching of the BP crystal. We observe that while few-layered BP is stable under the 80 kV electron beam (e-beam) in vacuum, the lattice oxidizes and degrades at room temperature in the presence of oxygen only in the region under the e-beam. The oxidative etch rate also increases with increasing e-beam dosage, suggesting the presence of an energy barrier for the oxidation reaction. Preferential oxidative etching along the [0 0 1] and [0 0 1] crystallographic directions is observed, in good agreement with density functional theory calculations showing favorable thermodynamic stability of the oxidized BP (0 0 1) planes compared to the (1 0 0) planes. We expect the atomistic insights and fundamental understanding obtained here to aid in the development of novel approaches to integrate BP in future applications.
ABSTRACT
Here, we demonstrate the utilization of biocompatible Prussian blue (PB) active coatings onto polyester-carbon nanotube (CNT) threads to enable a fiber-based platform for both power harvesting and continuous motion sensing. First, we show experimental evidence supporting that the mechanistic power generating mechanical-electrochemical coupling in an electrochemical generator (ECG) is best achieved with K-ion insertion, in contrast to the expected preference for Li-ion insertion for batteries. We then construct KPB fibers and demonstrate power generation in an ECG device up to 3.8 µW/cm2 at low frequencies relevant to human motion in either an aqueous or polymer gel electrolyte media. Further, by stitching these yarns into gloves or arm sleeves, our results show the continuous monitoring of finger or arm motion, respectively, during slow and repetitive human motion. Overall, our work demonstrates an ECG platform that overcomes the performance and integration barriers toward combined textile integration and human motion sensing while leveraging common materials and understanding extending from alkali metal-ion batteries.
Subject(s)
Electric Power Supplies , Electrochemical Techniques , Textiles , Electric Capacitance , Ferrocyanides/chemistry , Humans , Motion , Nanotubes, Carbon/chemistry , Particle Size , Polyesters/chemistry , Surface PropertiesABSTRACT
Advances in the synthesis and scalable manufacturing of single-walled carbon nanotubes (SWCNTs) remain critical to realizing many important commercial applications. Here we review recent breakthroughs in the synthesis of SWCNTs and highlight key ongoing research areas and challenges. A few key applications that capitalize on the properties of SWCNTs are also reviewed with respect to the recent synthesis breakthroughs and ways in which synthesis science can enable advances in these applications. While the primary focus of this review is on the science framework of SWCNT growth, we draw connections to mechanisms underlying the synthesis of other 1D and 2D materials such as boron nitride nanotubes and graphene.
ABSTRACT
Carbon nanotubes exhibit mechanical properties ideally suited for reinforced structural composites and surface area and conductivity attractive for electrochemical capacitors. Here we demonstrate the multifunctional synergy between these properties in a composite material exhibiting simultaneous mechanical and energy storage properties. This involves a reinforcing electrode developed using dense, aligned carbon nanotubes grown on stainless steel mesh that is layered in an ion conducting epoxy electrolyte matrix with Kevlar or fiberglass mats. The resulting energy storage composites exhibit elastic modulus over 5 GPa, mechanical strength greater than 85 MPa, and energy density up to 3 mWh/kg for the total combined system including electrodes, current collector, Kevlar or fiberglass, and electrolyte matrix. Furthermore, findings from in-situ mechano-electro-chemical tests indicate simultaneous mechanical and electrochemical functionality with invariant and stable supercapacitor performance maintained throughout the elastic regime.
ABSTRACT
Here we demonstrate a composite material exhibiting dual multifunctional properties of a structural material and a redox-active battery. This incorporates three-dimensional aligned carbon nanotube interfaces that weave together a structural frame, redox-active battery materials, and a Kevlar-infiltrated solid electrolyte that facilitates ion transfer. Relative to the total measured composite material mass, we demonstrate energy density up to â¼1.4 Wh/kg, elastic modulus of 7 GPa, and tensile strength exceeding 0.27 GPa. Mechano-electrochemical analysis demonstrates stable battery operation under mechanical loading that validates multifunctional performance. These findings demonstrate how battery materials that are normally packaged under compression can be reorganized as elements in a structurally reinforced composite material.
ABSTRACT
Here we demonstrate a full-cell battery design that bridges the energy density and rate capability between that of supercapacitors or pseudocapacitors with that of traditional lithium-ion batteries. This is accomplished by pairing an anode that enables ultrafast ion co-intercalation, an open framework cathode that allows rapid ion diffusion, and linear ether based electrolyte that sustains cell-level stability and high rate performance. We show this platform to be suitable for both sodium and potassium batteries using graphite as the co-intercalation anode, and Prussian blue as the open framework cathode. Our devices exhibit active material energy densities >100 W h kg-1 with power density >1000 W kg-1 with cycling durability approaching â¼80% energy density retention over 2000 cycles. This work brings together state-of-the-art concepts for fast-charging batteries into a full-cell configuration.
ABSTRACT
Small-diameter carbon nanotubes (CNTs) often require increased sophistication and control in synthesis processes, but exhibit improved physical properties and greater economic value over their larger-diameter counterparts. Here, we study mechanisms controlling the electrochemical synthesis of CNTs from the capture and conversion of ambient CO2 in molten salts and leverage this understanding to achieve the smallest-diameter CNTs ever reported in the literature from sustainable electrochemical synthesis routes, including some few-walled CNTs. Here, Fe catalyst layers are deposited at different thicknesses onto stainless steel to produce cathodes, and atomic layer deposition of Al2O3 is performed on Ni to produce a corrosion-resistant anode. Our findings indicate a correlation between the CNT diameter and Fe metal layer thickness following electrochemical catalyst reduction at the cathode-molten salt interface. Further, catalyst coarsening during long duration synthesis experiments leads to a 2× increase in average diameters from 3 to 60 min durations, with CNTs produced after 3 min exhibiting a tight diameter distribution centered near â¼10 nm. Energy consumption analysis for the conversion of CO2 into CNTs demonstrates energy input costs much lower than the value of CNTs-a concept that strictly requires and motivates small-diameter CNTs-and is more favorable compared to other costly CO2 conversion techniques that produce lower-value materials and products.
ABSTRACT
Here we demonstrate the broad capability to exploit interactions at different length scales in 2D materials to prepare macroscopic functional materials containing hybrid black phosphorus/graphene (BP/G) heterostructured building blocks. First, heterostructured 2D building blocks are self-assembled during co-exfoliation in the solution phase based on electrostatic attraction of different 2D materials. Second, electrophoretic deposition is used as a tool to assemble these building blocks into macroscopic films containing these self-assembled 2D heterostructures. Characterization of deposits formed using this technique elucidates the presence of stacked and sandwiched 2D heterostructures, and zeta potential measurements confirm the mechanistic interactions driving this assembly. Building on the exceptional sodium alloying capacity of BP, these materials were demonstrated as superior binder-free and additive-free anodes for sodium batteries with specific discharge capacity of 2365 mA h gP-1 and long stable cycling duration. This study demonstrates how controllable co-processing of 2D materials can enable material control for stacking and building block assembly relevant to broad future applications of 2D materials.
ABSTRACT
The widespread use of melt infiltration has to date restricted sulfur-carbon cathode architectures to only host materials processed as bulk powders with no site control of sulfur deposits. Here, we combine structurally designed hierarchical carbon nanotube (CNT) arrays with site-selective vapor phase sulfur infiltration to produce thick electrodes with controlled sulfur loading and high areal performance. Our results illustrate the critical role structural hierarchy plays in sustaining electrical connectivity to enable high utilization of the sulfur embedded in thick electrodes with high gravimetric loading. Here, a primary large-diameter CNT population provides robust conductive trunks that branch into a secondary small-diameter and high-surface-area CNT population capable of giving rapid electrical access to coated sulfur. Site-selective vapor phase sulfur infiltration, based on the capillary effect, controllably targets loading of one or both of the CNT populations to facilitate gravimetric loading from 60 wt% to 70 wt% sulfur. With the high areal loading of 6 mg cm-2, we demonstrate 1092 mA h gS-1 and 6.5 mA h cm-2 and excellent rate performance with >60% capacity retained at 10 times the discharge rate. Overall, our work leverages site control of sulfur incorporation into a host cathode enabled by controlled CNT growth techniques to emphasize the important principle of "quality over quantity" in designing high areal loading strategies with high areal performance and good sulfur utilization.
ABSTRACT
The interplay between mechanical strains and battery electrochemistry, or the tunable mechanochemistry of batteries, remains an emerging research area with limited experimental progress. In this report, we demonstrate how elastic strains applied to vanadium pentoxide (V2O5), a widely studied cathode material for Li-ion batteries, can modulate the kinetics and energetics of lithium-ion intercalation. We utilize atomic layer deposition to coat V2O5 materials onto the surface of a shapememory superelastic NiTi alloy, which allows electrochemical assessment at a fixed and measurable level of elastic strain imposed on the V2O5, with strain state assessed through Raman spectroscopy and X-ray diffraction. Our results indicate modulation of electrochemical intercalation potentials by â¼40 mV and an increase of the diffusion coefficient of lithium ions by up to 2.5-times with elastic prestrains of <2% imposed on the V2O5. These results are supported by density functional theory calculations and demonstrate how mechanics of nanomaterials can be used as a precise tool to strain engineer the electrochemical energy storage performance of battery materials.
ABSTRACT
Here, we demonstrate a strategy to produce high areal loading and areal capacity sulfur cathodes by using vapor-phase infiltration of low-density carbon nanotube (CNT) foams preformed by solution processing and freeze-drying. Vapor-phase capillary infiltration of sulfur into preformed and binder-free low-density CNT foams leads to a mass loading of â¼79 wt % arising from interior filling and coating of CNTs with sulfur while preserving conductive CNT-CNT junctions that sustain electrical accessibility through the thick foam. Sulfur cathodes are then produced by mechanically compressing these foams into dense composites (ρ > 0.2 g/cm3), revealing specific capacity of 1039 mAh/gS at 0.1 C, high sulfur areal loading of 19.1 mg/cm2, and high areal capacity of 19.3 mAh/cm2. This work highlights a technique broadly adaptable to a diverse group of nanostructured building blocks where preformed low-density materials can be vapor infiltrated with sulfur, mechanically compressed, and exhibit simultaneous high areal and gravimetric storage properties. This provides a route for scalable, low-cost, and high-energy density sulfur cathodes based on conventional solid electrode processing routes.
ABSTRACT
We demonstrate a room-temperature sodium sulfur battery based on a confining microporous carbon template derived from sucrose that delivers a reversible capacity over 700 mAh/gS at 0.1C rates, maintaining 370 mAh/gS at 10 times higher rates of 1C. Cycling at 1C rates reveals retention of over 300 mAh/gS capacity across 1500 cycles with Coulombic efficiency >98% due to microporous sulfur confinement and stability of the sodium metal anode in a glyme-based electrolyte. We show sucrose to be an ideal platform to develop microporous carbon capable of mitigating electrode-electrolyte reactivity and loss of soluble intermediate discharge products. In a manner parallel to the low-cost materials of the traditional sodium beta battery, our work demonstrates the combination of table sugar, sulfur, and sodium, all of which are cheap and earth abundant, for a high-performance stable room-temperature sodium sulfur battery.
ABSTRACT
Despite the promise of surface engineering to address the challenge of polysulfide shuttling in sulfur-carbon composite cathodes, melt infiltration techniques limit mechanistic studies correlating engineered surfaces and polysulfide anchoring. Here, we present a controlled experimental demonstration of polysulfide anchoring using vapor phase isothermal processing to fill the interior of carbon nanotubes (CNTs) after assembly into binder-free electrodes and atomic layer deposition (ALD) coating of polar V2O5 anchoring layers on the CNT surfaces. The ultrathin submonolayer V2O5 coating on the CNT exterior surface balances the adverse effect of polysulfide shuttling with the necessity for high sulfur utilization due to binding sites near the conductive CNT surface. The sulfur loaded into the CNT interior provides a spatially separated control volume enabling high sulfur loading with direct sulfur-CNT electrical contact for efficient sulfur conversion. By controlling ALD coating thickness, high initial discharge capacity of 1209 mAh/gS at 0.1 C and exceptional cycling at 0.2 C with 87% capacity retention after 100 cycles and 73% at 450 cycles is achieved and correlated to an optimal V2O5 anchoring layer thickness. This provides experimental evidence that surface engineering approaches can be effective to overcome polysulfide shuttling by controlled design of molecular-scale building blocks for efficient binder free lithium sulfur battery cathodes.
ABSTRACT
Sodium-ion batteries (SIBs) have been pursued as a more cost-effective and more sustainable alternative to lithium-ion batteries (LIBs), but these advantages come at the expense of energy density. In this work, we demonstrate that the challenge of energy density for sodium chemistries can be overcome through an anode-free architecture enabled by the use of a nanocarbon nucleation layer formed on Al current collectors. Electrochemical studies show this configuration to provide highly stable and efficient plating and stripping of sodium metal over a range of currents up to 4 mA/cm2, sodium loading up to 12 mAh/cm2, and with long-term durability exceeding 1000 cycles at a current of 0.5 mA/cm2. Building upon this anode-free architecture, we demonstrate a full cell using a presodiated pyrite cathode to achieve energy densities of â¼400 Wh/kg, far surpassing recent reports on SIBs and even the theoretical maximum for LIB technology (387 Wh/kg for LiCoO2/graphite cells) while still relying on naturally abundant raw materials and cost-effective aqueous processing.
ABSTRACT
The effectiveness of using catalyst nanoparticles to reduce the overpotential and energy efficiency of lithium-oxygen (or lithium-air) batteries (LOBs) is usually attributed to the inherent catalytic properties of individual nanoparticles. Here, we demonstrate that the morphology of the catalyst layer is equally important in maintaining integrity of the catalyst coating during product formation in LOBs. We demonstrate this by comparing the performance of smooth, conformal coated Mn2O3 catalyst nanoparticles prepared by electric field-assisted deposition, and more irregular coatings using conventional film assembly techniques both on three-dimensional mesh substrates. Smooth coatings lead to an improved overpotential of 50 mV during oxygen reduction and 130 mV during oxygen evolution in addition to a nearly 2X improvement in durability compared to the more irregular films. In situ electrochemical impedance spectroscopy combined with imaging studies elucidates a mechanism of morphology-directed deactivation of catalyst layers during charging and discharging that must be overcome at practical electrode scales to achieve cell-level performance targets in LOBs.
ABSTRACT
For lithium-sulfur batteries to surpass the energy density of lithium-ion batteries, sulfur-containing cathodes require high sulfur loading (>70 wt%) relative to all inactive components, anchoring sites to prevent polysulfide shuttling, high capacity (>1000 mA h g-1), and stable cycling performance. Here we demonstrate a nanomanufacturing route to produce low-density hybrid nanomaterial electrodes that synergize the mechanical and electrical integrity of carbon nanotubes (CNTs) with the chemical defect properties of carbon nanohorns (CNHs) to produce carefully optimized properties for binder-free lithium-sulfur battery cathodes. High sulfur loadings (>75%) are achieved through a brief (<20 minute) vapor phase treatment at 155 °C, with sulfur infiltration kinetics that increase with defect content of the hybrid composite. By controlling the relative concentration of CNHs to CNTs, and hence defect engineering the composite, we determine an optimized hybrid structure with a 7 : 3 relative weight ratio that exhibits a reversible capacity of more than 1200 mA h gsulfur-1 when operated at 0.1C and a capacity retention of over 85% after 100 cycles. The excellent cyclability and high capacity of these electrodes is one of the best reported to date for binder-free carbon composites and we demonstrate this to be due to the role of defects in promoting the retention of high order polysulfides for subsequent conversion to the insoluble low-order polysulfide reaction product. Our work highlights the critical intersection between controllably manufactured compositions of hybrid nanostructures and improved performance in batteries capable of surpassing the energy storage capability of conventional Li-ion.
ABSTRACT
Recently emerging potassium ion (K-ion) batteries offer a lower-cost alternative to lithium-ion batteries while enabling comparably high storage capacity. Here, we leverage the strong Raman spectroscopic response of few-layered graphene to provide the first insight into the electrochemical staging sequence for K+ ions in graphitic carbons. Our analysis reveals the signature of a dilute stage I compound that precedes formation of ordered intercalation compounds transitioning from stage VI (KC72), stage II (KC24), and stage I (KC8) and correlates electrochemical responses to the stage formation. Overall, our study emphasizes a minimum barrier to transfer the general understanding acquired for lithium-ion battery anodes to cheaper, earth abundant K-ion battery systems ideally suited for grid-scale storage.