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Biomarkers play an important and irrefutable role in the screening, diagnosis, monitoring and treatment of a wide variety of human diseases. As these biomarkers inevitably feature more and more prominently in the patient care pathway, there is a growing need for technologies that can provide rapid, accurate and sensitive test results at low cost. In this review we showcase, discuss, evaluate, and explain some recent advances in screen-printed electrodes (SPEs) and the modification strategies used for the electrochemical biosensing of some of the important, established biomarkers related to 1) cardiac injury, 2) cancer diagnostics and 3) acute inflammatory conditions, three areas of medicine currently associated with significant healthcare costs. Electroanalytical biosensors are proven to be an attractive alternative to benchtop conventional testing techniques, saving space, whilst allowing enhanced portability, a reduction in testing costs and test turnaround times. Electrochemical-based point-of-care (POC) testing technologies are still in the early stages of commercial, and hence clinical, uptake. Due to the design flexibility, low-cost and reliability of SPEs we expect to see a significant acceleration in the development of SPE-based electrochemical approaches to POC in these areas of medicine. Rapid, simultaneous detection of multiple important analytes in a single test at the point of patient's care will undoubtedly be the driver for uptake into clinical settings; their potential for impact is discussed herein.

Robust, reliable, and affordable analytical techniques are essential for screening and monitoring food and water safety from contaminants, pathogens, and allergens that might be harmful upon consumption. Recent advances in decentralised, miniaturised, and rapid tests for health and environmental monitoring can provide an alternative solution to the classic laboratory-based analytical techniques currently utilised. Electrochemical biosensors offer a promising option as portable sensing platforms to expedite the transition from laboratory benchtop to on-site analysis. A plethora of electroanalytical sensor platforms have been produced for the detection of small molecules, proteins, and microorganisms vital to ensuring food and drink safety. These utilise various recognition systems, from direct electrochemical redox processes to biological recognition elements such as antibodies, enzymes, and aptamers; however, further exploration needs to be carried out, with many systems requiring validation against standard benchtop laboratory-based techniques to offer increased confidence in the sensing platforms. This short review demonstrates that electroanalytical biosensors already offer a sensitive, fast, and low-cost sensor platform for food and drink safety monitoring. With continued research into the development of these sensors, increased confidence in the safety of food and drink products for manufacturers, policy makers, and end users will result.

Additively manufactured (AM) supercapacitor platforms are fabricated from bespoke filaments, which are comprised of electro-conductive graphene (20 wt%) incorporated polylactic acid (80 wt%), via fused deposition modeling and denoted as G/AMEs. The G/AMEs are shown to be capable of acting as a template for the electrodeposition of metals/metal oxides, in particular MoO2 nanowires (MoO2-G/AMEs), which are subsequently explored as a capacitor within 1 m H2SO4, 1-butyl-3-methylimidazolium hexafluorophosphate, and 1-butyl-3-methylimidazolium tetrafluoroborate. Optimization of the MoO2-G/AMEs demonstrates capacitance up to 1212 F g–1 when used in a symmetric arrangement. The material science described herein represents a significant enhancement in unlocking AMs potential as a valid manufacturing route for device level capacitance architectures.

This paper reports the detection of the inflammatory and sepsis-related biomarker, interleukin-6 (IL-6), in human blood plasma using functionalized screen-printed electrodes (SPEs) in conjunction with a thermal detection methodology, termed heat-transfer method (HTM). SPEs are functionalized with antibodies specific for IL-6 through electrodeposition of a diazonium linking group and N'-ethylcarbodiimide hydrochloride (EDC) coupling, which was tracked through the use of cyclic voltammetry and Raman spectroscopy. The functionalized SPEs are mounted inside an additively manufactured flow cell and connected to the HTM device. We demonstrate the ability to detect IL-6 at clinically relevant concentrations in PBS buffer (pH = 7.4) with no significant interference from the similarly sized sepsis-related biomarker procalcitonin (PCT). The limit of detection (3s) of the system is calculated to correspond to 3.4 ± 0.2 pg mL-1 with a working range spanning the physiologically relevant concentration levels in both healthy individuals and patients with sepsis, indicating the sensitivity of the sensor is suitable for the application. Further experiments helped provide a proof-of-application through the detection of IL-6 in blood plasma with no significant interference observed from PCT or the constituents of the medium. Due to the selectivity, sensitivity, straightforward operation, and low cost of production, this sensor platform has the potential for use as a traffic light sensor for the multidetection of inflammatory biomarkers for the diagnosis of sepsis and other conditions in which the rapid testing of blood biomarkers has vital clinical application.

2D hexagonal boron nitride (2D-hBN) is a lesser utilised material than other 2D counterparts in electrochemistry due to initial reports of it being non-conductive. As we will demonstrate in this review, this common misconception is being challenged, and researchers are starting to utilise 2D-hBN in the field of electrochemistry, particularly as the basis of electroanalytical sensing platforms. In this critical review, we overview the use of 2D-hBN as an electroanalytical sensing platform summarising recent developments and trends and highlight future developments of this interesting, often overlooked, 2D material.

The structure of vertically aligned graphene electrodes is shown to directly affect heterogeneous electron transfer kinetics in terms of the density of active edge plane sites of the microstructure, where greater edge content results in favourable electrochemical behaviour.

We present the fabrication of platinum (Pt⁰) nanoparticle (ca. 3 nm average diameter) decorated vertically aligned graphene (VG) screen-printed electrodes (Pt/VG-SPE) and explore their physicochemical characteristics and electrocatalytic activity towards the hydrogen evolution reaction (HER) in acidic media (0.5 M H₂SO₄). The Pt/VG-SPEs exhibit remarkable HER activity with an overpotential (recorded at −10 mA cm−²) and Tafel value of 47 mV (vs. RHE) and 27 mV dec−¹. These values demonstrate the Pt/VG-SPEs as significantly more electrocatalytic than a bare/unmodified VG-SPE (789 mV (vs. RHE) and 97 mV dec−¹). The uniform coverage of Pt⁰ nanoparticles (ca. 3 nm) upon the VG-SPE support results in a low loading of Pt⁰ nanoparticles (ca. 4 µg cm−²), yet yields comparable HER activity to optimal Pt based catalysts reported in the literature, with the advantages of being comparatively cheap, highly reproducible and tailorable platforms for HER catalysis. In order to test any potential dissolution of Pt⁰ from the Pt/VG-SPE surface, which is a key consideration for any HER catalyst, we additively manufactured (AM) a bespoke electrochemical flow cell that allowed for the electrolyte to be collected at regular intervals and analysed via inductively coupled plasma optical emission spectroscopy (ICP-OES). The AM electrochemical cell can be rapidly tailored to a plethora of geometries making it compatible with any size/shape of electrochemical platform. This work presents a novel and highly competitive HER platform and a novel AM technique for exploring the extent of Pt⁰ nanoparticle dissolution upon the electrode surface, making it an essential study for those seeking to test the stability/catalyst discharge of their given electrochemical platforms.

In 2020, the new European Drinking Water Directive will be updated to include new drinking-water safety parameters. These will introduce reduced thresholds for the presence of heavy metals, pesticides and other contaminants in domestic drinking water. The aim of these reduced thresholds is to impose a higher level of consumer protection as well as provide guidance for effective monitoring, planning and water management. An example of a newly proposed threshold is the concentration of lead ions (Pb2+) within drinking water, which has been reduced from 10 to 5 parts per billion (ppb). The strict timeframe for water suppliers to meet the new thresholds has created an impetus to develop in situ detection techniques to quantify the levels of chemical contamination on-site in drinking water, allowing them to make prompt interventions. This review explores and discusses the current advances related to electrochemical methods, electrode materials and modifications that have the potential to be the foundations of a new generation of portable electrochemical sensors towards trace-level ion in situ heavy metal sensors.

We report the electroanalytical properties of graphene and graphite paste electrodes comprising varying lateral flake sizes when applied for sensing relevant biomolecules and prominent drugs of abuse.

Herein, we report the fabrication and application of Li‐ion anodes for utilisation within Li‐ion batteries, which are fabricated via additive manufacturing/3D printing (fused deposition modelling) using a bespoke graphene/polylactic acid (PLA) filament, where the graphene content can be readily tailored and controlled over the range 1–40 wt. %. We demonstrate that a graphene content of 20 wt. % exhibits sufficient conductivity and critically, effective 3D printability for the rapid manufacturing of 3D printed freestanding anodes (3DAs); simplifying the components of the Li‐ion battery negating the need for a copper current collector. The 3DAs are physicochemically and electrochemically characterised and possess sufficient conductivity for electrochemical studies. Critically, it is found that if the 3DAs are used in Li‐ion batteries the specific capacity is very poor but can be significantly improved through the use of a chemical pre‐treatment. Such treatment induces an increased porosity, which results in a 200‐fold increase (after anode stabilisation) of the specific capacity (ca. 500 mAh g−1 at a current density of 40 mA g−1). This work significantly enhances the field of additive manufacturing/3D printed graphene based energy storage devices demonstrating that useful 3D printable batteries can be realised.