Hydrogen peroxide (H₂O₂) is a common chemical used in many industries and can be found in various biological environments, water, and air. Yet, H₂O₂ in a certain range of concentrations can be hazardous and toxic. Therefore, it is crucial to determine its concentration at different conditions for safety and diagnostic purposes. This review provides an insight about different types of sensors that have been developed for detection of H₂O₂. Their flexibility, stability, cost, detection limit, manufacturing, and challenges in their applications have been compared. More specifically the advantages and disadvantages of various flexible substrates that have been utilized for the design of H₂O₂ sensors were discussed. These substrates include carbonaceous substrates (e.g., reduced graphene oxide films, carbon cloth, carbon, and graphene fibers), polymeric substrates, paper, thin glass, and silicon wafers. Many of these substrates are often decorated with nanostructures composed of Pt, Au, Ag, MnO₂, Fe₃O₄, or a conductive polymer to enhance the performance of sensors. The impact of these nanostructures on the sensing performance of resulting flexible H₂O₂ sensors has been reviewed in detail. In summary, the detection limits of these sensors are within the range of 100 nM-1 mM, which makes them potentially, but not necessarily, suitable for applications in health, food, and environmental monitoring. However, the required sample volume, cost, ease of manufacturing, and stability are often neglected compared to other detection parameters, which hinders sensors' real-world application. Future perspectives on how to address some of the substrate limitations and examples of application-driven sensors are also discussed.

Gas detection and monitoring are essential due to their direct impact on human health, environment, and ecosystem. Chemiresistive sensors are one of the most used classes of sensors for monitoring and measurement of gases thanks to their ease of fabrication, customizability, mechanical flexibility, and fast response time. While chemiresistive sensors can offer good sensitivity and selectivity to a particular gas in a controlled environment with known interferences, they may not be able to differentiate between various gases having similar physiochemical properties under uncontrolled conditions. To address this shortcoming of chemiresistive gas sensors, sensor arrays have been the subject of recent studies. Gas sensor arrays are a group of individual gas sensors that are arranged to simultaneously detect and differentiate multiple cross‐reactive gases. In this regard, various sensor array technologies have been developed to differentiate a given set of gases using multivariate algorithms. This review provides an insight into the different algorithms that are used to extract the data from the sensor arrays, highlighting the fabrication techniques used for developing the sensor array prototypes, and different applications in which these arrays are used.

Invasive methods such as blood collection and biopsy are commonly used for testing liver and kidney function, which are painful, time-consuming, require trained personnel, and may not be easily accessible to people for their routine checkup. Early diagnosis of liver and kidney diseases can prevent severe symptoms and ensure better management of these patients. Emerging approaches such as breath and sweat analysis have shown potential as non-invasive methods for disease diagnosis. Among the many markers, ammonia is often used as a biomarker for the monitoring of liver and kidney functions. In this review we provide an insight into the production and expulsion of ammonia gas in the human body, the different diseases that could potentially use ammonia as biomarker and analytical devices such as chemiresistive gas sensors for non-invasive monitoring of this gas. The review also provides an understanding into the different materials, doping agents and substrates used to develop such multifunctional sensors. Finally, the current challenges and the possible future trends have been discussed.

Synthetic micro-diamond-polydimethylsiloxane (PDMS) composite microfluidic chips and thin films were produced using indirect 3D printing and spin coating fabrication techniques. Microfluidic chips containing up to 60 wt% micro-diamond were successfully cast and bonded. Physicochemical properties, including the dispersion pattern, hydrophobicity, chemical structure, elasticity and thermal characteristics of both chip and films were investigated. Scanning electron microscopy indicated that the micro-diamond particles were embedded and interconnected within the bulk material of the cast microfluidic chip, whereas in the case of thin films their increased presence at the polymer surface resulted in a reduced hydrophobicity of the composite. The elastic modulus increased from 1.28 for a PDMS control, to 4.42 MPa for the 60 wt% composite, along with a three-fold increase in thermal conductivity, from 0.15 to 0.45 W m⁻¹ K⁻¹. Within the fluidic chips, micro-diamond incorporation enhanced heat dissipation by efficient transfer of heat from within the channels to the surrounding substrate. At a flow rate of 1000 μL/min, the gradient achieved for the 60 wt% composite chip equalled a 9.8 °C drop across a 3 cm long channel, more than twice that observed with the PDMS control chip.