“…In addition, as previously shown in Figure B, the produced LIG layer is very thin (less than 50 μm). Therefore, the obtained specific capacitance should in principle be lower than the values obtained for thicker and porous substrates such as paper , and other cellulose-based materials, ,− for instance. Moreover, higher capacitances have also been obtained for doped graphene/LIG electrodes , or systems prepared by more complicated or expensive methods. , Nevertheless, the specific capacitance achieved represents a good result considering the lower LIG thickness and undoped nature.…”
Laser irradiation of polymeric materials has drawn great
attention
as a fast, simple, and cost-effective method for the formation of
porous graphene films that can be subsequently fabricated into low-cost
and flexible electronic and energy-storage devices. In this work,
we report a systematic study of the formation of laser-induced graphene
(LIG) with sheet resistances as low as 9.4 Ω/sq on parylene-C
ultrathin membranes under a CO2 infrared laser. Raman analysis
proved the formation of the multilayered graphenic material, with I
D/I
G and I
2D/I
G peak ratios
of 0.42 and 0.65, respectively. As a proof of concept, parylene-C
LIG was used as the electrode material for the fabrication of ultrathin,
solid-state microsupercapacitors (MSCs) via a one-step, scalable,
and cost-effective approach, aiming at future flexible and wearable
applications. The produced LIG-MSC on parylene-C exhibited good electrochemical
behavior, with a specific capacitance of 1.66 mF/cm2 and
an excellent cycling stability of 96% after 10 000 cycles (0.5
mA/cm2). This work allows one to further extend the knowledge
in LIG processes, widening the group of precursor materials as well
as promoting future applications. Furthermore, it reinforces the potential
of parylene-C as a key material for next-generation biocompatible
and flexible electronic devices.
“…In addition, as previously shown in Figure B, the produced LIG layer is very thin (less than 50 μm). Therefore, the obtained specific capacitance should in principle be lower than the values obtained for thicker and porous substrates such as paper , and other cellulose-based materials, ,− for instance. Moreover, higher capacitances have also been obtained for doped graphene/LIG electrodes , or systems prepared by more complicated or expensive methods. , Nevertheless, the specific capacitance achieved represents a good result considering the lower LIG thickness and undoped nature.…”
Laser irradiation of polymeric materials has drawn great
attention
as a fast, simple, and cost-effective method for the formation of
porous graphene films that can be subsequently fabricated into low-cost
and flexible electronic and energy-storage devices. In this work,
we report a systematic study of the formation of laser-induced graphene
(LIG) with sheet resistances as low as 9.4 Ω/sq on parylene-C
ultrathin membranes under a CO2 infrared laser. Raman analysis
proved the formation of the multilayered graphenic material, with I
D/I
G and I
2D/I
G peak ratios
of 0.42 and 0.65, respectively. As a proof of concept, parylene-C
LIG was used as the electrode material for the fabrication of ultrathin,
solid-state microsupercapacitors (MSCs) via a one-step, scalable,
and cost-effective approach, aiming at future flexible and wearable
applications. The produced LIG-MSC on parylene-C exhibited good electrochemical
behavior, with a specific capacitance of 1.66 mF/cm2 and
an excellent cycling stability of 96% after 10 000 cycles (0.5
mA/cm2). This work allows one to further extend the knowledge
in LIG processes, widening the group of precursor materials as well
as promoting future applications. Furthermore, it reinforces the potential
of parylene-C as a key material for next-generation biocompatible
and flexible electronic devices.
“…25,42,43 Efficient LIG conversion is also enabled by efficient photochemical and nonlinear absorption, which provides better electrical conductivity with lower laser power. As a result, our femtosecond-LIG offers superior graphene quality with a sheet resistance of 2.86 Ω/□ over the previously reported LIGs realized by CW lasers; Kevlar-LIG patterned by 10.6 μm 8.0 W CO 2 laser provided the sheet resistance of 300 Ω/□, 44 and additional phosphorus-doping with 10.6 μm 6.4 W CO 2 laser could improve the sheet resistance of LIG to ∼4.0 Ω/□, 45 and the 10.6 μm 7.0 W CO 2 laser could realize ∼15 Ω/□ value of sheet resistance of LIG from aramid paper 46 (Table S2). Additionally, the line width is decreased to 28.2 μm with a power of 1.5 W and a scanning speed of 150 mm/s under the focusing spot size of 70.95 μm due to the nonthermal machining of ultrashort pulses (Figure S10 and Table S3).…”
Personal wearable devices are considered
important in
advanced
healthcare, military, and sports applications. Among them, e-textiles
are the best candidates because of their intrinsic conformability
without any additional device installation. However, e-textile manufacturing
to date has a high process complexity and low design flexibility.
Here, we report the direct laser writing of e-textiles by converting
raw Kevlar textiles to electrically conductive laser-induced graphene
(LIG) via femtosecond laser pulses in ambient air. The resulting LIG
has high electrical conductivity and chemical reliability with a low
sheet resistance of 2.86 Ω/□. Wearable multimodal e-textile
sensors and supercapacitors are realized on different types of Kevlar
textiles, including nonwoven, knit, and woven structures, by considering
their structural textile characteristics. The nonwoven textile exhibits
high mechanical stability, making it suitable for applications in
temperature sensors and micro-supercapacitors. On the other hand,
the knit textile possesses inherent spring-like stretchability, enabling
its use in the fabrication of strain sensors for human motion detection.
Additionally, the woven textile offers special sensitive pressure-sensing
networks between the warp and weft parts, making it suitable for the
fabrication of bending sensors used in detecting human voices. This
direct laser synthesis of arbitrarily patterned LIGs from various
textile structures could result in the facile realization of wearable
electronic sensors and energy storage.
“…This method enables fast patterning and is suitable for integrated circuits, fulfilling the voltage requirements of various applications. Lu et al 75 explored the potential of chemical foaming and LIG technology to enhance the capacitance of p-MSCs (Figure 5d). By applying a chemical foaming agent to commercial aramid paper, they significantly improved the MSC's performance, achieving higher capacitance, reduced electrochemical impedance, and superior cycle performance compared to unmodified devices.…”
Recent advances in paper-based microsupercapacitors (p-MSCs) have attracted significant attention due to their potential as substrates for flexible electronics. This review summarizes progress in the field of p-MSCs, discussing their challenges and prospects. It covers various aspects, including the fundamental characteristics of paper, the modification of paper with functional materials, and different methods for device fabrication. The review critically analyzes recent advancements, materials, and fabrication techniques for p-MSCs, exploring their potential applications and benefits, such as flexibility, costeffectiveness, and sustainability. Additionally, this review highlights gaps in current research, guiding future investigations and innovations in the field. It provides an overview of the current state of p-MSCs and offers valuable insights for researchers and professionals in the field. The critical analysis and discussion presented herein offer a roadmap for the future development of p-MSCs and their potential impact on the domain of flexible electronics.
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