Portable Applications Research Articles

RF energy harvesters for wireless sensors, state of the art, future prospects and challenges: a review.

The power consumption of portable gadgets, implantable medical devices (IMDs) and wireless sensor nodes (WSNs) has reduced significantly with the ongoing progression in low-power electronics and the swift advancement in nano and microfabrication. Energy harvesting techniques that extract and convert ambient energy into electrical power have been favored to operate such low-power devices as an alternative to batteries. Due to the expanded availability of radio frequency (RF) energy residue in the surroundings, radio frequency energy harvesters (RFEHs) for low-power devices have garnered notable attention in recent times. This work establishes a review study of RFEHs developed for the utilization of low-power devices. From the modest single band to the complex multiband circuitry, the work reviews state of the art of required circuitry for RFEH that contains a receiving antenna, impedance matching circuit, and an AC-DC rectifier. Furthermore, the advantages and disadvantages associated with various circuit architectures are comprehensively discussed. Moreover, the reported receiving antenna, impedance matching circuit, and an AC-DC rectifier are also compared to draw conclusions towards their implementations in RFEHs for sensors and biomedical devices applications.

3D Radial Junctions for Robust and Flexible Optoelectronics

AbstractMarrying nanostructures with thin films is a recent trend in flexible optoelectronics to improve light trapping and mechanical stability. Radial junction (RJ) a‐Si:H thin film optoelectronics, directly deposited upon the vapor‐liquid‐solid (VLS) grown silicon nanowires (SiNWs), can pave the way to achieving excellent flexibility and a high power‐to‐weight ratio (PTWR). Thanks to their vertical‐standing geometry, SiNWs framework can enhance the mechanical stability of RJ units, by keeping the working region far away from the stress‐rich substrate surface. Using low‐melting‐point metals as catalysts, the SiNW array can be fabricated at a low temperature down to 350 °C in a PECVD system, making it possible to directly construct robust RJ units on flexible, low‐cost substrates, such as Al foil. In this review, the recent progress of the flexible RJ a‐Si:H thin film solar cells/photodetectors that are directly fabricated on the surface of low‐cost flexible substrates is reviewed. Moreover, these RJ flexible optoelectronics are demonstrated for use in wearable and real‐time health monitoring, and as cardiac pacemakers for heart stimulation. This RJ technology highlights a promising potential to establish high‐performance, low‐cost, mechanically stable flexible optoelectronic for wearable, portable applications.

Piezoelectric generator harvesting bike vibrations energy to supply portable devices

With the decrease in energy consumption of portable electronic devices, the concept of harvesting renewable energy in human surrounding arouses a renewed interest. In this context, we have developed a piezoelectric generator that harvests mechanical vibrations energy available on a bicycle. Embarked piezoelectric transducer, which is an electromechanical converter, undergoes mechanical vibrations therefore produce electricity. A static converter transforms the electrical energy in a suitable form to the targeted portable application. Values of generated electrical power are reported and commented.

Comparative of heat transfer performance between a parallel serpentine-baffle flow field plate and a parallel flow field plate design in a direct ethanol proton exchange membrane fuel cell

The dependence on fossil fuels as an energy source causes serious environmental problems. Direct ethanol proton exchange membrane fuel cells (DE-PEMFCs) that directly convert the chemical energy stored in the etanol alcohol into electricity makes it promising as an environment-friendly power source for portable and mobile applications. Increasing the reagent operating temperature increases the electrochemical kinetics at the anode, increasing the cell power. However in a DE-PEMFC, the flow field plate directly interferes at the heat flow. As a result, the aim of this research were project a new parallel serpentine flow field plate with interdigitated characteristics, a parallel serpentine-baffle flow field plate (PSBFFP) and comparing with a PSFFP with respect to heat transfer performance in a DE-PEMFC anode side. The results show that the discontinue channels presents in the PSBFFP improve the heat transfer between plate and reagent, improving the reaction rate and consequently the fuel cell performance.

Revolutionizing energy storage: exploring the nanoscale frontier of all-solid-state batteries.

Due to their distinctive security characteristics, all-solid-state batteries are seen as a potential technology for the upcoming era of energy storage. The flexibility of nanomaterials shows enormous potential for the advancement of all-solid-state batteries' exceptional power and energy storage capacities. These batteries might be applied in many areas such as large-scale energy storage for power grids, as well as in the creation of foldable and flexible electronics, and portable gadgets. The most difficult aspect of creating a comprehensive nanoscale all-solid-state battery assembly is the task of decreasing the particle size of the solid electrolyte while maintaining its excellent ionic conductivity. Materials possessing nanoscale structural features and a substantial electrochemically active surface area have the potential to significantly enhance power characteristics and the cycle life. This might bring about substantial changes to existing energy storage models. The primary objective of this research is to summarize the latest advancements in utilizing nanomaterials for energy harvesting in various all-solid-state battery assemblies. This study examines the most complex solid-solid interfaces of all-solid-state batteries, as well as feasible methods for implementing nanomaterials in such interfaces. Currently, there is significant attention on the necessity to develop electrode-solid electrolyte interfaces that exhibit nanoscale particle articulation and other characteristics related to the behavior of lithium ions.

Interlayer reinforcement for improved mechanical reliability for wearable perovskite solar cells

Flexible perovskite solar cells (F-PSCs) are emerging as a promising solution for weight-sensitive, wearable, portable, and flexible applications. However, F-PSCs still suffer from poor mechanical reliability due to weak interlayer...

Nanoscale engineering of solid-state materials for boosting hydrogen storage.

The development of novel materials capable of securely storing hydrogen at high volumetric and gravimetric densities is a requirement for the wide-scale usage of hydrogen as an energy carrier. In recent years, great efforts via nanoscale tuning and designing strategies on both physisorbents and chemisorbents have been devoted to improvements in their thermodynamic and kinetic aspects. Increasing the hydrogen storage capacity/density for physisorbents and chemisorbents and improving the dehydrogenation kinetics of hydrides are still considered a challenge. The extensive and fast development of advanced nanotechnologies has fueled a surge in research that presents huge potential in designing solid-state materials to meet the ultimate U.S. Department of Energy capacity targets for onboard light-duty vehicles, material-handling equipments, and portable power applications. Different from the existing literature, in this review, particular attention is paid to the recent advances in nanoscale engineering of solid-state materials for boosting hydrogen storage, especially the nanoscale tuning and designing strategies. We first present a short overview of hydrogen storage mechanisms of nanoscale engineering for boosted hydrogen storage performance on solid-state materials, for example, hydrogen spillover, nanopump effect, nanosize effect, nanocatalysis, and other non-classical hydrogen storage mechanisms. Then, the focus is on recent advancements in nanoscale engineering strategies aimed at enhancing the gravimetric hydrogen storage capacity of porous materials, reducing dehydrogenation temperature and improving reaction kinetics and reversibility of hydrogen desorption/absorption for metal hydrides. Effective nanoscale tuning strategies for enhancing the hydrogen storage performance of porous materials include optimizing surface area and pore volume, fine-tuning nanopore sizes, introducing nanostructure doping, and crafting nanoarchitecture and nanohybrid materials. For metal hydrides, successful strategies involve nanoconfinement, nanosizing, and the incorporation of nanocatalysts. This review further addresses the points to future research directions in the hope of ushering in the practical applications of hydrogen storage materials.

An evaluation of the examples of mobile smart agriculture applications in Turkiye

The technological process of agricultural mechanization has evolved from mechanical, hydraulic, and pneumatic structures to electrical-electronic and mechatronic systems. With the addition of digital technologies in recent years, agricultural mechanization tools have had functions as time-independent, non-spatial, and unmanned. Agricultural production technologies are now equipped with integrated systems with the Internet of Things, cloud informatics, image processing, wireless data transmission, and mobile-portable devices. Today, during the production process, physical, biological, or chemical data detected through sensors from plants, animals, soil, and atmosphere are uploaded to computers and cloud informatic technologies as big data sets. The data is presented to decision-makers via mobile devices connected to the internet. Within the scope of this study, examples of mobile-portable applications used in the field of smart agriculture in the world and our country were generally examined. In addition, technological and sectoral applications for mobile smart agriculture in our country have been taken over. Currently, common application examples of the Ministry of Agriculture and Forestry, and some private sector companies, that produce these technologies and provide them for the end users, have also been researched in this context. In addition to these, the strengths and weaknesses of the current portable mobile applications in agricultural production have been tried to be analyzed in terms of our country’s conditions.

In situ growth of binder-free CoNi0.5-MOF/CC electrode for high-performance flexible solid-state supercapacitor application.

Metal organic frameworks (MOFs) with binder-free electrodes have shown promise for portable electrochemical energy storage applications. However, their low specific capacitance and challenges associated with the attachment of active materials to the substrate constrain their practical utility. In this research, we prepared a CoNi0.5-MOF/CC electrode by in situ growth of CoNi0.5-MOF on an H2O2-pretreated carbon cloth (CC) without using any binder. It exhibits a higher specific capacitance of 1337.5 F g-1 than that of CoNi0.5-MOF (∼578 F g-1) at a current density of 1 A g-1 and an excellent rate ability of 88% specific capacitance retention at a current density of 10 A g-1 after 6000 cycles. The as-assembled flexible asymmetric solid-state supercapacitor based on the CoNi0.5-MOF/CC positive electrode and a nitrogen-doped graphene (N-Gr) negative electrode exhibits an energy density of 61.46 W h kg-1 at a power density of 1244.56 W kg-1 and holds a stable capacitance of ∼125 F g-1 at 1 A g-1 when the flexible supercapacitor is bent, showing great potential for flexible electronics application. The H2O2 is indicated to play an important role, enhancing the adhesion of CoNi0.5-MOF on CC and reducing its charge transfer resistance by functionalizing the carbon fiber during the pretreatment of the CC matrix. The results provide a great way to prepare a flexible asymmetric solid-state supercapacitor with both high power density and high energy density for practical application.

Applications, limitations and advancements of ultra-low-field magnetic resonance imaging: A scoping review.

Ultra-low-field magnetic resonance imaging (ULF-MRI) has emerged as an alternative with several portable clinical applications. This review aims to comprehensively explore its applications, potential limitations, technological advancements, and expert recommendations. A review of the literature was conducted across medical databases to identify relevant studies. Articles on clinical usage of ULF-MRI were included, and data regarding applications, limitations, and advancements were extracted. A total of 25 articles were included for qualitative analysis. The review reveals ULF-MRI efficacy in intensive care settings and intraoperatively. Technological strides are evident through innovative reconstruction techniques and integration with machine learning approaches. Additional advantages include features such as portability, cost-effectiveness, reduced power requirements, and improved patient comfort. However, alongside these strengths, certain limitations of ULF-MRI were identified, including low signal-to-noise ratio, limited resolution and length of scanning sequences, as well as variety and absence of regulatory-approved contrast-enhanced imaging. Recommendations from experts emphasize optimizing imaging quality, including addressing signal-to-noise ratio (SNR) and resolution, decreasing the length of scan time, and expanding point-of-care magnetic resonance imaging availability. This review summarizes the potential of ULF-MRI. The technology's adaptability in intensive care unit settings and its diverse clinical and surgical applications, while accounting for SNR and resolution limitations, highlight its significance, especially in resource-limited settings. Technological advancements, alongside expert recommendations, pave the way for refining and expanding ULF-MRI's utility. However, adequate training is crucial for widespread utilization.

Structures, performances and applications of green biomass derived carbon in lithium-ion batteries

Most countries worldwide have committed to reaching carbon neutrality by the end of the century, with the aim to achieve Net Zero before 2060. To reduce the dependency of energy demands on fossil fuels, use of renewable energy and its gradual transition into the overall energy portfolio becomes increasingly critical. The solar and wind energy accounts for a major part of renewable energy. Considering unstable and noncontinuous production of electricity from these two sources, energy storage becomes essential. Lithium-ion batteries (LIBs) have become the most favorable choice of energy storage due to their good electrochemical performance (high capacity, low charge leakage and good cycle performance) and safety, in particular for portable (3C products, electric vehicles and drones) and stationary applications as well as for emergency electricity supply. However, the specific capacity of graphite, the most common commercial anode material, is reaching its theoretical limit, posing great challenges for improving the overall capacity of LIBs. It is therefore necessary to develop anode materials of higher capacity and better cycle performance. Biomass-derived carbon materials are ideal candidates for further enhancing the performance of LIBs due to their special microstructures, functional diversity and easy structure regulation. Most of these materials can reach capacities exceeding 500 mAh g-1, even the best for more than 1,000 mAh g-1 combined with other anode materials. This review provides an in-depth analysis of diverse carbon sources derived from biomass, categorized based on their distinct structural characteristics, with the focus on evaluating the current roles and bottlenecks of carbon as a component of the electrode materials used in LIBs. The failure mechanisms associated with biomass-derived carbon in LIBs are summarized, with potential solutions to these issues being proposed. The potential challenges and prospects for biomass-based LIBs are identified and thoroughly discussed. Overall, this review aims to serve as a resource for the strategic design and advancement of carbon-based materials, to achieve next-generation LIBs of superior performance.

A 2D carbon nitride-based electrochemical aptasensor with reverse amplification for highly sensitive detection of okadaic acid in shellfish.

Okadaic acid (OA) is one of the main virulence factors of diarrheal shellfish toxins (DSP). It is of great significance to detect OA with an accurate, specific and cost-effective technique in the fields of seafood safety and water quality control. In this work, an electrochemical aptasensor with reverse amplification was developed for the sensitive detection of OA. A two-dimensional graphite-phase nanomaterial (carbon nitride) modified with an anti-OA aptamer and thionine (Th) was immobilized onto the surface of the electrochemical electrode as the sensitive element to capture target OA molecules. ssDNA-modified carbon nitride was used as the reverse amplification element by hybridizing with non-OA linked aptamers. The preparation of the electrochemical aptasensor was well characterized by Scanning Electron Microscopy (SEM), zeta potential detection, UV-Vis absorption, Brunner-Emmet-Teller (BET) measurements, and electrochemical measurements. The quantitative assessment of OA was achieved by differential pulse voltammetry (DPV). Experimental results indicated that this aptasensor showed a concentration-dependent response to OA with a good detection performance including in terms of selectivity, repeatability, reproducibility, and stability. It exhibited 100-fold selectivity between OA and other toxins including dinophysistoxins (DTX), pectenotoxins (PTX), and yessotoxins (YTX). In addition, it showed a much wider quantification range, which is 10-13 M-10-10 M (0.080-80.50 pg mL-1). The detection limit was as low as 10-13 M (0.080 pg mL-1). The aptasensor also successfully achieved significant practicality on real shellfish samples contaminated by OA. All these results demonstrated that the reverse amplification strategy for marine toxin detection may provide a label-free and rapid detection approach for portable applications in the fields of environmental monitoring and food security.

A Recent Comprehensive Review of Fuel Cells: History, Types, and Applications

This review discusses the history, fundamentals, and applications of different fuel cell technologies, including proton exchange membrane fuel cells (PEMFCs), direct methanol fuel cells, solid oxide fuel cells (SOFCs), phosphoric acid fuel cells (PAFCs), alkaline fuel cells (AFCs), and molten carbonate fuel cells (MCFCs). Recent advances in fuel cell technologies have led to potential applications in aerospace, transportation, and portable and stationary power generation due to high efficiency and low emissions. Fuel cell types are also compared based on efficiency, operating temperature, lifetime, energy/power density, and cost. It was noticed that PEMFCs have the highest mass power density, reaching 1,000 W/kg compared to less than 100 W/kg for SOFCs, which makes them suitable for portable applications such as aircraft. PEMFCs and AFCs are suitable for low‐temperature applications and are highly efficient. SOFCs and MCFCs are better for high‐temperature operations. SOFCs are robust and suitable for high‐power demands, while MCFCs are advantageous for high‐power output. Hydrogen fuel cells promise to decarbonize transportation and aviation sectors with the advantages of lower weight, compactness, and quick startup times. However, challenges remain around renewable hydrogen production/infrastructure and aircraft integration, besides hydrogen storage, water management inside fuel cells, and operational robustness under varying pressures. Generally, for all fuel cell types, more focus should be given to enhancing the stability and efficiency of fuel cell materials and reducing their cost.

IMPACT OF SUPPLY VOLTAGE ON SRAM CELL POWER DISSIPATION UNDER DIFFERENT TOPOLOGIES

The high storage density and quick access times of Static Random Access Memory (SRAM) make it a critical component of many Very Large Scale Integration circuits. However, device scaling in today's technology leads to an increase in dynamic power and a decrease in noise margin, posing significant challenges to memory circuit design for the next generation of devices. In addition, sub-threshold leakage is also a concern. In recent years, the increasing demand for notebooks, laptops, IC memory cards, and mobile communication devices has driven the development of low-power, low-voltage memory circuits. Static Random Access Memoryis widely used as on-chip and off-chip memory for portable applications because they are easy to use and have minimal standby leakage. Since 60% to 70% of the chip memory is used, SRAM optimization is the focus of research. The SRAM cell's architecture and performance have been studied using various technologies to minimize power dissipation while maintaining stability. Based on the power dissipation, including static and dynamic power dissipation, and Static Noise Margin (SNM), the SRAM cell performance is compared with different topologies. The SNM fluctuation is considered along with the variation of supply voltage.

CacheIEE: Cache-Assisted Isolated Execution Environment on ARM Multi-Core Platforms

ARM TrustZone technology has been widely used to create Trusted Execution Environments (TEEs) for enhancing the security of applications. However, the increasing number of installed security-sensitive applications in the secure world will inevitably enlarge the trusted computing base (TCB) of TEE systems. To minimize the TCB of the secure world and increase application portability, Isolated Execution Environments (IEEs) are proposed to protect applications in enclaves created in the normal world. However, existing IEE systems cannot provide the same level of security as the TEE systems, particularly, on resolving the multi-vector attacks that include both physical memory disclosure attacks and software attacks. In this paper, we develop a new cache-assisted IEE system called CacheIEE that creates enclaves in the L1 data cache of the normal world to protect sensitive data against multi-vector attacks. First, by always storing the sensitive data in the L1 data cache, CacheIEE can effectively prevent physical memory disclosure attacks. Second, we protect the L1 data cache against untrusted rich OS running in other cores. To support more applications, CacheIEE can process large-size sensitive data in the L1 data cache with constrained capacity. We implement a system prototype of CacheIEE and verify its security and practicability.

Room-Temperature Self-Powered Infrared Spectrometer Based on a Single Black Phosphorus Heterojunction Diode.

Infrared spectrometers with the ability to resolve the spectral intensity and wavelength simultaneously are widely used in industry and the laboratory. However, their huge volume, high price, and cryogenic operating temperature limit their applications in the rapidly developing field of portable devices. Here, we demonstrate a room-temperature self-powered infrared spectrometer based on a single black phosphorus (BP) heterojunction diode. The nonlinearly gate-tunable photocurrent spectrum involving quantum-confined Franz-Keldysh and Burstein-Moss effects in a single BP/MoS2 diode instead of using space-consuming detector arrays provides a new dimension for resolving the intensity and wavelength information of spectra simultaneously. The active area for spectral sensing is only 1500 μm2, and the photodetection range is from 1.7 to 3.6 μm. Room-temperature operation, micrometer-scale size, and silicon-compatible technology make the BP/MoS2 heterojunction a promising configuration for portable spectrometer applications.

Modulation of Prelithiation Solution for Hard Carbon Anodes of Lithium-Ion Batteries

The increasing demand for high-energy and high-power lithium-ion batteries (LIBs) in portable gadgets and electric vehicles has led to exploration of high-performance silicon and hard carbon (HC) anodes to replace traditional graphite anodes. However, their practical application is hindered by low initial coulombic efficiency and large irreversible capacity, which decreases the total energy density. Prelithiation is a strategy to restore energy density by supplying additional Li ions. Chemical prelithiation, involving immersing the electrode in a reductive Li−aromatic hydrocarbon (arene) complex solution, is a standout method due to its safety, high efficiency, and practical feasibility. It not only restores the lost lithium but also aids in maintaining a more stable solid electrolyte interphase layer to guarantee battery cycling stability. The first part of our study addresses the issue of expensive and impractical arene complexes for prelithiation, we focus on using low-cost and commercially available aromatic compounds such as naphthalene and methyl-substituted naphthalene compounds. This study investigates the effects of electron-donating methyl groups on naphthalene on the prelithiation activity toward HC using density functional theory calculations. In the second part of this study, we use low-cost and easily available solvents such as ethylene glycol dimethyl ether, bis(2-methoxyethyl) ether, and triethylene glycol dimethyl ether for chemical prelithiation. Ether solvents have a desirable solvation effect with Li+, and the ether with low solvation power enhances the prelithiation activity. The degree of prelithiation is greatly affected by the reaction time, and the details of this relationship are rarely investigated. In the final part of our study, we conduct a detailed investigation on the effects of various reaction times on the prelithiation activity toward the HC anode. This study provides useful insights for effective prelithiation, in terms of choosing aromatic compounds, solvents, and reaction time.

Synergistic Effect of Lithium (difluoromethanesulfonyl)(trifluoromethanesulfonyl)Imide (LiDFTFSI) and Vinylene Carbonate (VC) on High Performance of NMC811║Graphite Cells

Lithium-ion batteries (LIBs) have gained increasing importance in energy storage systems, driven by the growing demands of grid storage, automotive, and portable consumer applications. To meet the need for high energy density batteries, one promising approach involves the utilization of high capacity layered transition metal oxide cathodes, such as nickel-rich LiNi0.8Mn0.1Co0.1O2 (NMC811), which can deliver a high reversible specific capacity of over 180 mAh·g-1 [1,2]. However, due to the structural and interfacial instability[3], nickel-rich NMC cathode still faces challenges in long-term galvanostatic cycling. For these reasons, design of novel electrolyte formulations, which enable formation of an effective cathode electrolyte interphase (CEI), is highly desirable. Recent studies have highlighted the cross-talk between the cathode and anode, indicating that the evolution of the solid electrolyte interphase (SEI) can impact the formation of the CEI[4]. Thus, establishing an effective SEI/CEI pair is essential for achieving long-term cycling of nickel-rich NMC cathode-based cells. Electrolyte optimization plays a crucial role in facilitating the formation of a desirable SEI/CEI pair, leading to an improved cell performance and longevity. Lithium (difluoromethanesulfonyl)(trifluoro-methanesulfonyl)imide (LiDFTFSI) has proven to be promising in solid-polymer-electrolyte batteries due to the good SEI/CEI formation ability and suppressed Al-dissolution[5]. Additionally, LiDFTFSI exhibits also good compatibility with Li-metal batteries[6], heralding promising applications in Li-ion batteries. However, there is lack of systematic research investigating the potential impact of LiDFTFSI on the cathode as well as on resulting CEI formation and dynamics.In this work, we demonstrated enhanced galvanostatic cycling performance of NMC811||graphite cells achieved by utilizing LiDFTFSI and lithium hexafluorophosphate (LiPF6) in a blended salt organic carbonate-based electrolyte formulation. Comprehensive electrochemical and post mortem analysis revealed that the LiDFTFSI alone can effectively mitigate the structural changes in the NMC811 electrode by facilitating the formation of modified CEI. However, the continued growth of an inhomogeneous CEI, caused by the cross-talk effect between electrodes, adversely affected long-term cycling stability. To address this, vinylene carbonate (VC) was introduced to the electrolyte. Synergistic effect with LiDFTFSI leads to the formation of effective and uniform SEI and CEI. As a result, 720 charge/discharge cycles were achieved in NMC811||graphite cells with LiDFTFSI and VC containing electrolytes at 1C while maintaining 80% state-of-health (SOH80%).

Sensitive Recognition of Acetamiprid with a Unique Electrochromic Molecular Imprinted Polymer Sensor

The development of molecularly imprinted polymers (MIPs) and the applications for them have attracted a great deal of interest during the last two decades. MIPs are generally used in different fields, specially molecularly imprinted electrochemical sensors (MIECS), due to their particular design and specific detection abilities [1]. The advantages of an electrochemical MIP sensor include low cost, easy operation, rapid response time and excellent potential for miniaturization and construction for portable equipment applications [2]. In the scope of this work, we performed that electropolymerization of IrO2 as an electrochromic material on an indium tin oxide (ITO) glass substrate and electrosynthesis on this electrode using pyrrole as a functional monomer in the presence of acetamiprid as template were used to create the electrochromic molecular imprinted polymer sensor (MIP/IrO2/ITO). With the created electrochromic MIP sensor, it is intended to create a selective pesticide sensor by utilizing molecular imprinted polymer (MIP) technology, and to detect with the naked eye by color change depending on the acetamiprid concentration by using electrochromic material. The IrO2/ITO electrochromic film demonstrated magnificent cycle stability (100 cycles), high coloration efficiency (400 cm2 C-1 at 450 nm), and quick coloring/bleaching reaction time (8.60s/7.10s, respectively). By using in-situ spectroelectrochemical measurements, these optical properties of MIP/IrO2/ITO were obtained at various acetamiprid concentrations for quantitative analysis. By using differential pulse voltammetry between -0.2 V and +0.8 V (versus Ag/AgCl in 0.1 M PBS), the sensor performance of MIP/IrO2/ITO was assessed. In an acetamiprid concentration range of 4.29–38.6 nM, the MIP/IrO2/ITO electrode demonstrated linear response with a detection limit of 2.72 nM, sensitivity of 47.2 µA nM-1, and repeatability of 0.87%. Keywords: Electrochromism; Molecularly imprinted polymer (MIP); Pyrrole; IrO2;Acetamiprid; Electrochemical sensor; Spectroelectrochemistry. Acknowledgements This work was supported by The Scientific and Technological Research Council of Türkiye, TUBITAK (Project No:121Z784) as the financial.

(Invited) On the Role of Thermo-Electrochemical Coupling in Li-Ion Batteries

Li-ion batteries have revolutionized a wide range of industries, from consumer electronics to vehicles. Their relatively high power and energy density and exceptional Coulombic efficiency are particularly advantageous for portable applications. Significant efforts have gone into studying the impact of thermal conditions on the electrochemical characteristics of Li-ion batteries because, in part, of the wide range of temperatures these devices are operated in. Recently, we have shown that thermo-electrochemical coupling in Li-ion batteries is of critical importance. In this talk, we will highlight some of our recent work that measures the local thermal conditions within the cell using embedded instrumentation and illustrates how significant thermal variations within the cell, specifically thermal gradients, are on electrochemical behavior. Moreover, we will discuss our efforts to pinpoint the underlying mechanisms that give rise to these effects.Acknowledgments:The authors thank Dr. Michele Anderson (Office of Naval Research, grant N00014-22-1-2411) for financial support of this work.