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Laser‐induced graphene (LIG) is inexpensive, fast, and easy to produce when compared to many other forms of graphene. Within the biosensing field, LIG electrodes are most often produced via infrared (IR) laser irradiation of polyimide sheets. Nevertheless, the usage of ultraviolet (UV) laser to produce LIG provides advantages in terms of sensor miniaturization because of its inherently higher scribing resolution. Yet, studies on the electrochemical performance of UV LIG, its relation with morphological and structural aspects as well as its comparison with IR LIG are still lacking. This work shows that both LIGs present swift electron transfer kinetics constituting excellent electrodes for electroanalysis. Extreme sensitivities of 93 and 58 µA µm−1 cm−2 at physiologically relevant dopamine (DA) concentrations are found for IR and UV LIG, respectively. Such sensitivities and good selectivity are achieved in the presence of physiologically relevant concentrations of ascorbic and uric acids, contrasting to the related literature employing IR LIG where such interferents are below the physiological range. Despite providing lower sensitivity, UV LIG is still an excellent material for DA biosensors, with the above‐mentioned advantages in terms of miniaturization. To our knowledge, these are among the highest sensitivities reported for voltammetric measurement of DA using carbon‐based materials. [ABSTRACT FROM AUTHOR]

Carbon-based electrodes have demonstrated great promise as electrochemical transducers in the development of biosensors. More recently, laser-induced graphene (LIG), a graphene derivative, appears as a great candidate due to its superior electron transfer characteristics, high surface area and simplicity in its synthesis. The continuous interest in the development of cost-effective, more stable and reliable biosensors for glucose detection make them the most studied and explored within the academic and industry community. In this work, the electrochemistry of glucose oxidase (GOx) adsorbed on LIG electrodes is studied in detail. In addition to the well-known electroactivity of free flavin adenine dinucleotide (FAD), the cofactor of GOx, at the expected half-wave potential of −0.490 V vs. Ag/AgCl (1 M KCl), a new well-defined redox pair at 0.155 V is observed and shown to be related to LIG/GOx interaction. A systematic study was undertaken in order to understand the origin of this activity, including scan rate and pH dependence, along with glucose detection tests. Two protons and two electrons are involved in this reaction, which is shown to be sensitive to the concentration of glucose, restraining its origin to the electron transfer from FAD in the active site of GOx to the electrode via direct or mediated by quinone derivatives acting as mediators. [ABSTRACT FROM AUTHOR]

Zinc oxide (ZnO)/laser-induced graphene (LIG) composites were prepared by mixing ZnO, grown by laser-assisted flow deposition, with LIG produced by laser irradiation of a polyimide, both in ambient conditions. Different ZnO:LIG ratios were used to infer the effect of this combination on the overall composite behavior. The optical properties, assessed by photoluminescence (PL), showed an intensity increase of the excitonic-related recombination with increasing LIG amounts, along with a reduction in the visible emission band. Charge-transfer processes between the two materials are proposed to justify these variations. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy evidenced increased electron transfer kinetics and an electrochemically active area with the amount of LIG incorporated in the composites. As the composites were designed to be used as transducer platforms in biosensing devices, their ability to detect and quantify hydrogen peroxide (H2O2) was assessed by both PL and CV analysis. The results demonstrated that both methods can be employed for sensing, displaying slightly distinct operation ranges that allow extending the detection range by combining both transduction approaches. Moreover, limits of detection as low as 0.11 mM were calculated in a tested concentration range from 0.8 to 32.7 mM, in line with the values required for their potential application in biosensors. [ABSTRACT FROM AUTHOR]

Laser-induced graphene from paper (paper-LIG) was applied in non-enzymatic electrochemical sensing of uric acid (UA) in human urine. Paper-LIG was formed by CO 2 laser modification of paper into a 3D graphene arrangement. Kinetic analysis of paper-LIG electrodes returned effective heterogeneous electron transfer standard rate constants of 1.4 × 10−3 cm s−1 and 7.8 × 10−4 cm s−1 for [Ru(NH 3) 6 ]2+/3+ and [Fe(CN) 6 ]4−/3− redox probes, respectively. These electrodes were able to detect and quantify uric acid in PBS within the 10–300 μM range at pH between 5.6 and 7.4. At pH 7.4, a linear response (R2 = 0.999) from 10 to 250 μM was achieved, with a limit of detection of 3.97 μM and a sensitivity of 0.363 μA cm−2 μM−1. Paper-LIG electrodes denoted adequate selectivity in synthetic urine as well as in ascorbic acid (AA) and dopamine (DA)-containing electrolytes. Determination of urinary UA content in human samples returned a concentration of c.a. 1.8–1.9 mM, within the range for healthy individuals. Recoveries of samples spiked with 50 and 100 μM UA were 100.6% and 95.4%, respectively, with satisfactory reproducibility and stability. These cheap, lightweight, flexible, and eco-friendly paper-LIG biosensors for non-enzymatic quantification of UA in human urine pave the way to widespread application in the detection of other important biomarkers. [Display omitted] • "Green" graphene electrodes by CO 2 laser irradiation of paper ("paper-LIG"). • Uric acid (UA) quantification at clinically relevant concentrations and pH (5.6–7.4). • Limit of detection of 3.97 μM and a sensitivity of 0.363 μA cm−2 μM−1 (pH = 7.4). • Adequate selectivity in synthetic urine, as well as in ascorbic acid and dopamine-containing electrolytes. • Recoveries of 100.6% and 95.4% for human urine samples spiked with 50 and 100 μM UA. [ABSTRACT FROM AUTHOR]