Surface-Enhanced Raman Spectroscopy-Scanning Electrochemical Microscopy: Observation of Real-Time Surface pH Perturbations.

Understanding and controlling chemical dynamics at electrode interfaces is key to electrochemical applications in sensing, electrocatalysis, and energy storage. Here, we introduce colocalized surface-enhanced Raman scattering-scanning electrochemical microscopy (SERS-SECM) as a multimodal tool able to simultaneously probe and affect electrochemical interfaces in real time. As a model system to demonstrate SERS-SECM, we used a self-assembled monolayer of 4-mercaptopyridine (4MPy), a pH sensitive Raman indicator, anchored to silver nanoparticles as a substrate. We modulated the local pH at the surface with chronoamperometry, inducing the hydrogen evolution reaction (HER) at the SECM tip and observed subsequent Raman peak height changes in the 4MPy. We then performed cyclic voltammetry of HER at the SECM tip while measuring SERS spectra every 200 ms to highlight the technique's real-time capabilities. Our results show the capability to sensitively interrogate and trigger chemical/electrochemical dynamic surface phenomena. We hope SERS-SECM will provide insight on the link between heterogeneous and homogeneous reactivity at electrochemical interfaces.

Impact of Plasmonic Photothermal Effects on the Reactivity of Au Nanoparticle Modified Graphene Electrodes Visualized Using Scanning Electrochemical Microscopy.

Atomically thin graphene electrodes enable the modulation of interfacial reactivity by means of underlying substrate effects. Here we show that plasmonic excitation of microscopic arrays composed of 50 nm Au nanoparticles situated underneath a graphene interface results in localized enhancements on the electrochemical readout. We used scanning electrochemical microscopy (SECM) in the feedback and H2O2 collection modes to identify the role of the generated plasmons on the electrochemical response. Using electrochemical imaging, supported by finite-element method simulations, we confirmed that a temperature rise of up to ∼30 K was responsible for current enhancements observed for mass transfer- limited reactions. On single-layer graphene (SLG) we observed a shift in the onset of H2O2 generation which we traced back to photothermal induced kinetic changes, raising ko' from 1.1 × 10-8 m/s to 2.2 × 10-7 m/s. Thicker 10-layer graphene electrodes displayed only a small kinetic difference with respect to SLG, suggesting that photothermal processes, in contrast to hot carriers, are the main contributor to the observed changes in interfacial reactivity upon illumination. SECM is demonstrated to be a powerful technique for elucidating thermal contributions to reactive enhancements, and presents a convenient platform for studying sublayer and temperature-dependent phenomena over individual sites on electrodes.

Achieving Fast and Efficient K+ Intercalation on Ultrathin Graphene Electrodes Modified by a Li+ Based Solid-Electrolyte Interphase.

Advancing beyond Li-ion batteries requires translating the beneficial characteristics of Li+ electrodes to attractive, yet incipient, candidates such as those based on K+ intercalation. Here, we use ultrathin few-layer graphene (FLG) electrodes as a model interface to show a dramatic enhancement of K+ intercalation performance through a simple conditioning of the solid-electrolyte interphase (SEI) in a Li+ containing electrolyte. Unlike the substantial plating occurring in K+ containing electrolytes, we found that a Li+ based SEI enabled efficient K+ intercalation with discrete staging-type phase transitions observed via cyclic voltammetry at scan rates up to 100 mVs-1 and confirmed as ion-intercalation processes through in situ Raman spectroscopy. The resulting interface yielded fast charge-discharge rates up to ∼360C (1C is fully discharge in 1 h) and remarkable long-term cycling stability at 10C for 1000 cycles. This SEI promoted the transport of K+ as verified via mass spectrometric depth profiling. This work introduces a convenient strategy for improving the performance of ion intercalation electrodes toward a practical K-ion battery and FLG electrodes as a powerful analytical platform for evaluating fundamental aspects of ion intercalation.

Probing Graphene Interfacial Reactivity via Simultaneous and Colocalized Raman-Scanning Electrochemical Microscopy Imaging and Interrogation.

Addressing challenges in interfacial electrochemistry requires multimodal approaches that correlate the local structure and reactivity of materials with high spatial and temporal versatility. Here, we introduce spatiotemporally correlated Raman spectroscopy and scanning electrochemical microscopy (SECM) to study the impact that structural heterogeneities, interfacial decomposition products, and layer number have on the electron-transfer properties of graphene electrodes. By colocalizing the SECM probe and laser line, we successfully obtained congruent SECM and Raman images at a rate of 5 s per pixel with sub-10 µm resolution, obtaining full spectra per pixel at a signal-to-noise ratio as high as ∼20. SECM imaging of a micropatterned graphene electrode showed its reactivity to be highly dependent on the intensity of the G peak, an indicator of the number of graphene layers. We further monitored the impact of excursions to positive potentials using the [Fe(CN)6]3-/4- redox pair as mediator. Raman-SECM allowed us to decouple the contributions to the redox response of different structural effects including exfoliation, increase in defect density, and surface film formation, on the same site and in real time. The coupling of in situ Raman spectroscopy and SECM provides a powerful surface-sensitive analytical approach to elucidate interfacial properties relevant to energy, catalysis, and sensing.

Interrogating Charge Storage on Redox Active Colloids via Combined Raman Spectroscopy and Scanning Electrochemical Microscopy.

Redox active colloids (RACs) are dispersible, cross-linked polymeric materials that incorporate a high concentration of redox-active motifs, making them attractive for next-generation size-exclusion redox flow batteries. In order to tap into their full potential for energy storage, it is essential to understand their internal charge mobility, capacity, and cyclability. Here we focus on using a combined suite of Raman spectroscopy and scanning electrochemical microscopy (SECM) tools for evaluating three important parameters that govern charge storage in viologen-RACs: their intraparticle redox active concentration, their reduction/oxidation mechanism, and their charge transfer rate. We addressed RACs using SECM imaging and single-particle experiments, from which the intraparticle diffusion and concentration parameters were elucidated. By using Raman spectroscopy coupled to surface interrogation SECM, we further evaluated their reversible redox properties within monolayer films of 80- and 135-nm-sized RACs. Most notably we have confirmed that the concentration and redox mechanisms are essentially unchanged when varying the RAC size. As expected, we see that larger particles inherently require longer times for electrolysis independent of the methodology used for their study. Our simulations further verify the internal concentration of RACs and suggest that their porosity enables solution redox active mediators to penetrate and titrate charge in their interior. The combined methodology presented here sets an important analytical precedent in decoupling the charge storage properties of new bulk materials for polymer batteries starting from probing low-dimensional assemblies and single particles using nano- and spectroelectrochemical approaches.

Soft Surfaces for Fast Characterization and Positioning of Scanning Electrochemical Microscopy Nanoelectrode Tips.

The testing of nanoelectrode tips for scanning electrochemical microscopy (SECM) is a slow and cumbersome task that often results in untimely electrode breakage due to crashing against a substrate. Here, we evaluated approach curves of nano- and microelectrodes to soft surfaces using SECM for a rapid and more convenient characterization and positioning protocol. Soft surfaces consisted of either a submerged argon bubble or a thin polydimethylsiloxane (PDMS) layer. While approach curves to Ar bubbles in the presence of a surfactant were promising for the characterization of microelectrode tips, their performance with nanoelectrodes was deficient. In contrast, approach curves to PDMS films allowed the rapid positioning of nanoelectrodes as small as 30 nm radius at speeds up to 5 µm/s without the risk of breakage. The nanoelectrodes were able to approach the polymer films multiple times without affecting their electrochemical performance. Furthermore, using a half-coated substrate with PDMS, nanoelectrodes could be retracted and positioned very close to the bare, hard substrate for characterization with traditional approach curves. We estimate time savings on tip characterization/positioning on the order of 10- to 100-fold. This simple procedure is easily implemented without the requirement of additional devices supplementing existing commercial SECM instruments.

Composite Ionogel Electrodes for Polymeric Solid-State Li-Ion Batteries.

Realizing rechargeable cells with practical energy and power density requires electrodes with high active material loading, a remaining challenge for solid-state batteries. Here, we present a new strategy based on ionogel-derived solid-state electrolytes (SSEs) to form composite electrodes that enable high active material loading (>10 mg/cm2, ~9 mA/cm2 at 1C) in a scalable approach for fabricating Li-ion cells. By tuning the precursor and active materials composition incorporated into the composite lithium titanate electrodes, we achieve near-theoretical capacity utilization at C/5 rates and cells capable of stable cycling at 5.85 mA/cm2 (11.70 A/g) with over 99% average Coulombic efficiency at room temperature. Finally, we demonstrate a complete polymeric solid-state cell with a composite anode and a composite lithium iron phosphate cathode with ionogel SSEs, which is capable of stable cycling at a 1C rate.

Scanning Electrochemical Microscopy Reveals That Model Silicon Anodes Demonstrate Global Solid Electrolyte Interphase Passivation Degradation during Calendar Aging.

Silicon is a promising next-generation anode to increase energy density over commercial graphite anodes, but calendar life remains problematic. In this work, scanning electrochemical microscopy was used to track the site-specific reactivity of a silicon thin film surface over time to determine if undesirable Faradaic reactions were occurring at the formed solid electrolyte interphase (SEI) during calendar aging in four case scenarios: formation between 1.5 V and 100 mV with subsequent rest starting at (1) 1.5 V and (2) 100 mV and formation between 0.75 V and 100 mV with subsequent rest starting at (3) 0.75 V and (4) 100 mV. In all cases, the electrical passivation of silicon decreased with increasing time and potential relative to Li/Li+ over a 3 day period. Along with the decrease in passivation, the homogeneity of passivation over a 500 µm2 area decreased with time. Despite some local "hot spots" of reactivity, the areal uniformity of passivation suggests global SEI failure (e.g., SEI dissolution) rather than localized (e.g., cracking) failure. The silicon delithiated to 1.5 V vs Li/Li+ was less passivated than the lithiated silicon (at the beginning of rest, the forward rate constants, kf, for ferrocene redox were 7.19 × 10-5 and 3.17 × 10-7 m/s, respectively) and was also found to be more reactive than the pristine silicon surface (kf of 5 × 10-5 m/s). This reactivity was likely the result of SEI oxidation. When the cell was only delithiated up to 0.75 V versus Li/Li+, the surface was still passivating (kf of 6.11 × 10-6 m/s), but still less so than the lithiated surface (kf of 3.03 × 10-9 m/s). This indicates that the potential of the anode should be kept at or below ∼0.75 V vs Li/Li+ to prevent decreasing SEI passivation. This information will help with tuning the voltage windows for prelithiation in Si half cells and the operating voltage of Si full cells to optimize calendar life. The results provided should encourage the research community to investigate chemical, rather than mechanical, modes of failure during calendar aging and to stop using the typical convention of 1.5 V as a cutoff potential for cycling Si in half cells.

Ultralow-Temperature Li/CFx Batteries Enabled by Fast-Transport and Anion-Pairing Liquefied Gas Electrolytes.

Lithium fluorinated-carbon (Li/CFx ) is one of the most promising chemistries for high-energy-density primary energy-storage systems in applications where rechargeability is not required. Though Li/CFx demonstrates high energy density (>2100 Wh kg-1 ) under ambient conditions, achieving such a high energy density when exposed to subzero temperatures remains a challenge, particularly under high current density. Here, a liquefied gas electrolyte with an anion-pair solvation structure based on dimethyl ether with a low melting point (-141 °C) and low viscosity (0.12 mPa s, 20 °C), leading to high ionic conductivity (>3.5 mS cm-1 ) between -70 and 60 °C is reported. Besides that, through systematic X-ray photoelectron spectroscopy integrated with transmission electron microscopy characterizations, the interface of CFx is evaluated for low-temperature performance. The fast transport and anion-pairing solvation structure of the electrolyte are concluded to bring about reduced charge-transfer resistance at low temperatures, which results in significantly enhanced performance of Li/CFx cells (1690 Wh kg-1 , -60 °C based on active materials). Utilizing 50 mg cm-2 loading electrodes, the Li/CFx still displays 1530 Wh kg-1 at -60 °C. This work provides insights into the electrolyte design that may overcome the operational limits of batteries in extreme environments.

The advent of membrane-less zinc-anode aqueous batteries with lithium battery-like voltage.

Zinc (Zn)-anode batteries, although safe and non-flammable, are precluded from promising applications because of their low voltage (<2 V) and poor rechargeability. Here, we report the fabrication of rechargeable membrane-less Zn-anode batteries with high voltage properties (2.5 to 3.4 V) achieved through coupling cathodes and Zn-anodes in gelled concentrated acid and alkaline solutions separated by a gelled buffer interlayer containing the working ions. The concentrated gelled buffer interlayers perform dual functions of regulating the pH of the system and acting as the source and sink of the working ions. With this strategy we show low-cost membrane-less 2.5 to 3.4 V Zn-manganese dioxide (MnO2) batteries capable of cycling 10-100% of 617 mA h g-1-MnO2 and 20-30% of 820 mA h g-1-Zn and demonstrate their application in electric vehicles. This strategy is then applied to other oxide-based cathode systems like Cu2O and V2O5, where voltages of 2 to 3 V are obtained in membrane-less batteries.

Hydroxyl Conducting Hydrogels Enable Low-Maintenance Commercially Sized Rechargeable Zn-MnO2 Batteries for Use in Solar Microgrids.

Zinc (Zn)-manganese dioxide (MnO2) rechargeable batteries have attracted research interest because of high specific theoretical capacity as well as being environmentally friendly, intrinsically safe and low-cost. Liquid electrolytes, such as potassium hydroxide, are historically used in these batteries; however, many failure mechanisms of the Zn-MnO2 battery chemistry result from the use of liquid electrolytes, including the formation of electrochemically inert phases such as hetaerolite (ZnMn2O4) and the promotion of shape change of the Zn electrode. This manuscript reports on the fundamental and commercial results of gel electrolytes for use in rechargeable Zn-MnO2 batteries as an alternative to liquid electrolytes. The manuscript also reports on novel properties of the gelled electrolyte such as limiting the overdischarge of Zn anodes, which is a problem in liquid electrolyte, and finally its use in solar microgrid applications, which is a first in academic literature. Potentiostatic and galvanostatic tests with the optimized gel electrolyte showed higher capacity retention compared to the tests with the liquid electrolyte, suggesting that gel electrolyte helps reduce Mn3+ dissolution and zincate ion migration from the Zn anode, improving reversibility. Cycling tests for commercially sized prismatic cells showed the gel electrolyte had exceptional cycle life, showing 100% capacity retention for >700 cycles at 9.5 Ah and for >300 cycles at 19 Ah, while the 19 Ah prismatic cell with a liquid electrolyte showed discharge capacity degradation at 100th cycle. We also performed overdischarge protection tests, in which a commercialized prismatic cell with the gel electrolyte was discharged to 0 V and achieved stable discharge capacities, while the liquid electrolyte cell showed discharge capacity fade in the first few cycles. Finally, the gel electrolyte batteries were tested under IEC solar off-grid protocol. It was noted that the gelled Zn-MnO2 batteries outperformed the Pb-acid batteries. Additionally, a designed system nameplated at 2 kWh with a 12 V system with 72 prismatic cells was tested with the same protocol, and it has entered its third year of cycling. This suggests that Zn-MnO2 rechargeable batteries with the gel electrolyte will be an ideal candidate for solar microgrid systems and grid storage in general.