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Owing to the outstanding advantages as electrical energy storage system, supercapacitors have attracted tremendous research interests over the past decade. Current research efforts are being devoted to improve the energy storage capabilities of supercapacitors through either discovering novel electroactive materials or nanostructuring existing electroactive materials. From the device point of view, the energy storage performance of supercapacitor not only depends on the electroactive materials themselves, but importantly, relies on the structure of electrode whether it allows the electroactive materials to reach their full potentials for energy storage. With respect to utilizing nanostructured electroactive materials, the key issue is to retain all advantages of the nanoscale features for supercapacitors when being assembled into electrodes and the following devices. Rational design and fabrication of self‐supported nanoelectrodes is therefore considered as the most promising strategy to address this challenge. In this review, we summarize the recent advances in designing and fabricating self‐supported nanoelectrodes for supercapacitors towards high energy storage capability. Self‐supported homogeneous and heterogeneous nanoelectrodes in the forms of one‐dimensional (1D) nanoarrays, two‐dimensional (2D) nanoarrays, and three‐dimensional (3D) nanoporous architectures are introduced with their representative results presented. The challenges and perspectives in this field are also discussed. Self‐supported nanoelectrodes possess significant superiorities as binder‐ and conductive additive‐free electrodes for constructing supercapacitors with high energy storage capability. This review summarizes the recent advances in designing and fabricating self‐supported homogeneous and heterogeneous nanoelectrodes via either template‐free or template‐assisted methods, and highlights their advantages for supercapacitor applications. Challenges and future prospects in this field are discussed.

Scanning electrochemical microscopy (SECM) is a powerful and versatile technique for visualizing the local electrochemical activity of a surface as an ultramicroelectrode tip is moved towards or over a sample of interest using precise positioning systems. In comparison with other scanning probe techniques, SECM not only enables topographical surface mapping but also gathers chemical information with high spatial resolution. Considerable progress has been made in the analysis of biological samples, including living cells and immobilized biomacromolecules such as enzymes, antibodies and DNA fragments. Moreover, combinations of SECM with comple­mentary analytical tools broadened its applicability and facilitated multi-functional analysis with extended life science capabilities. The aim of this review is to present a brief topical overview on recent applications of biological SECM, with particular emphasis on important technical improvements of this surface imaging technique, recommended applications and future trends.

Primary physicochemical steps in microwounding of plants were investigated using electrochemical nano- and microprobes, with a focus on the role of oxygen in the wounding responses of individual plant cells. Electrochemical measurements of cell oxygen content were made with carbon-filled quartz micropipettes with platinum-coated tips (oxygen nanosensors). These novel platinum nanoelectrodes are useful for understanding cell oxygen metabolism and can be employed to study the redox biochemistry and biology of cells, tissues and organisms. We show here that microinjury of Chara corallina internodal cells with the tip of a glass micropipette is associated with a drastic decrease in oxygen concentration at the vicinity of the stimulation site. This decrease is reversible and lasts for up to 40 minutes. Membrane stretching, calcium influx, and cytoskeleton rearrangements were found to be essential for the localized oxygen depletion induced by cell wall microwounding. Inhibition of electron transport in chloroplasts or mitochondria did not affect the magnitude or timing of the observed response. In contrast, the inhibition of NADPH oxidase activity caused a significant reduction in the amplitude of the decrease in oxygen concentration. We suggest that the observed creation of localized anoxic conditions in response to cell wall puncture might be mediated by NADPH oxidase.

The multifaceted role of biological membranes prompted early the development of artificial lipid-based models with a primary view of reconstituting the natural functions in vitro so as to study and exploit chemoreception for sensor engineering. Over the years, a fair amount of knowledge on the artificial lipid membranes, as both, suspended or supported lipid films and liposomes, has been disseminated and has helped to diversify and expand initial scopes. Artificial lipid membranes can be constructed by several methods, stabilized by various means, functionalized in a variety of ways, experimented upon intensively, and broadly utilized in sensor development, drug testing, drug discovery or as molecular tools and research probes for elucidating the mechanics and the mechanisms of biological membranes. This paper reviews the state-of-the-art, discusses the diversity of applications, and presents future perspectives. The newly-introduced field of artificial cells further broadens the applicability of artificial membranes in studying the evolution of life.

We suggest a new method for preparing metal electrodes based on carbon nanoelectrodes (CNEs), which are suitable for application in shearforce scanning electrochemical microscopy (SECM). The as‐prepared CNEs were focused ion beam (FIB)‐processed, subsequently thermally recessed, and finally, Pt or Au were electrodeposited into the cavity of the recessed CNEs leading to insulator‐free metal electrodes with sizes of around 2 µm in diameter. For their application as local voltammetric pH sensors, the electrodes were calibrated in a concentration range of 11.6 M H+ to 9 M OH−. As a case study, we determined the local pH in situ using the developed Pt microelectrode positioned in close proximity to an Ag‐based gas diffusion electrode (GDE) which was operated for the oxygen reduction reaction (ORR). We could observe a shift of the Ptox reduction peak of ΔE = −700 mV, which is exceeding previous observations at Ag‐based GDEs by far. This novel type of electrode will pave the way to perform shearforce SECM with an even higher spatial resolution due to their spearhead shape. A novel method for the fabrication of insulator‐free Au/Pt carbon nanoelectrode‐based electrodes is proposed. The proposed electrodes are suitable for SECM shearforce positioning. As a possible application, their use as a voltammetric pH sensor positioned in close proximity to an operating Ag‐based gas diffusion electrode for the oxygen reduction reaction is demonstrated.

The current–voltage behavior of three DNA nanowire models, which consist of a fishbone structure and two separate double-chain setups, alongside an RNA model illustrated by a half-ladder configuration, is examined using zigzag carbon nanotubes and associated metallic armchair graphene nanoribbon electrodes. This study utilizes the tight-binding Hamiltonian technique within the Landauer–Büttiker theory. The different DNA and RNA nanowire models exhibit nonlinear current–voltage characteristics, which are calculated and analyzed based on the corresponding transmission probability. The findings show that the current–voltage properties are affected by the type of leads and their working temperature, with zigzag nanotubes producing somewhat greater currents than nanoribbon electrodes. With a near-zero bias at the electrodes, the current–voltage characteristics are influenced by the dimerization effects of longitudinal hopping in the devices. Due to the expected strong connection between electronic transport characteristics and the structures of DNA and RNA, these results might stimulate additional investigation into their biological importance for nanoelectronic devices.

Electrode miniaturization has profoundly revolutionized the field of electrochemical sensing, opening up unprecedented opportunities for probing biological events with a high spatial and temporal resolution, integrating electrochemical systems with microfluidics, and designing arrays for multiplexed sensing. Several technological issues posed by the desire for downsizing have been addressed so far, leading to micrometric and nanometric sensing systems with different degrees of maturity. However, there is still an endless margin for researchers to improve current strategies and cope with demanding sensing fields, such as lab-on-a-chip devices and multi-array sensors, brain chemistry, and cell monitoring. In this review, we present current trends in the design of micro-/nano-electrochemical sensors and cutting-edge applications reported in the last 10 years. Micro- and nanosensors are divided into four categories depending on the transduction mechanism, e.g., amperometric, impedimetric, potentiometric, and transistor-based, to best guide the reader through the different detection strategies and highlight major advancements as well as still unaddressed demands in electrochemical sensing. Graphical Abstract

Dielectrophoresis at the nanoscale has gained significant attention in recent years as a low-cost, rapid, efficient, and label-free technique. This method holds great promise for various interdisciplinary applications related to micro- and nanoscience, including biosensors, microfluidics, and nanomachines. The innovation and development of such devices and platforms could promote wider applications in the field of nanotechnology. This review aims to provide an overview of recent developments and applications of nanoparticle dielectrophoresis, where at least one dimension of the geometry or the particles being manipulated is equal to or less than 100 nm. By offering a theoretical foundation to understand the processes and challenges that occur at the nanoscale—such as the need for high field gradients—this article presents a comprehensive overview of the advancements and applications of nanoparticle dielectrophoresis platforms over the past 15 years. This period has been characterized by significant progress, as well as persistent challenges in the manipulation and separation of nanoscale objects. As a foundation for future research, this review will help researchers explore new avenues and potential applications across various fields.

Incorporating the nanoscale properties of carbon nanotubes (CNTs) and their assemblies into macroscopic materials is at the forefront of scientific innovation. The electrical conductivity, chemical inertness, and large aspect ratios of these cylindrical structures make them ideal electrode materials for electrochemical studies. The ability to assemble CNTs into nano-, micro-, and macroscale materials broadens their field of applications. Here, we report the fabrication of random arrays of CNT cross-sections and their performance as nanoelectrode ensembles (NEEs). Single ribbons of drawable CNTs were employed to create the CNT-NEEs that allows easier fabrication of nanoscale electrodes for general electrochemical applications. Surface analysis of the prepared NEEs using scanning electron microscopy showed a random distribution of CNTs within the encapsulating polymer. Electrochemical testing via cyclic voltammetry and scanning electrochemical cell microscopy revealed voltametric differences from the typical macroelectrode response with the steady-state nature of NEEs. Finally, when the NEE was employed for Pb2+ detection using square-wave anodic stripping voltammetry, a limit of detection of 0.57 ppb with a linear range of 10–35 ppb was achieved.

The scarcity of state‐of‐the‐art oxygen evolution reaction (OER) electrocatalysts has led to intensive research on alternative viable electrocatalytic materials. While activity and cost are the main factors to be sought after, the catalyst stability under harsh acidic conditions is equally crucial. Considering that OER is a proton‐coupled electron‐transfer reaction that involves local acidification of the reaction environment by liberation of H+, the catalyst stability can be largely compromised in such conditions. Consequently, probing the pH value near the catalyst surface under operation leads to a deeper understanding of this process. The applicability of bare Au microelectrodes and nanoelectrodes as sensitive local pH probes during OER is shown in this work by using scanning electrochemical microscopy (SECM). Two case studies are presented, including the state‐of‐the‐art OER catalyst (IrO2) in acidic media and a ZnGa2O4 catalyst in alkaline buffered solution, demonstrating the suitability of the Au probe to accurately determine the local pH value in a wide pH range. Au micro‐ and nanoelectrodes were developed as local voltammetric pH sensors during the oxygen evolution reaction (OER). Case studies including IrO2 in acidic media and ZnGa2O4 in alkaline buffer solution demonstrate the suitability of the Au tip to accurately determine the local pH value in a wide pH range and buffering environments.