Abstract:MEAs with nanofiber mat electrodes containing Pt/C catalyst and Nafion binder were fabricated and evaluated. The electrodes were prepared by electrospinning a solution of catalyst powder, salt-form Nafion (with Na+, Li+, or Cs+ as the sulfonic acid counterion), and a carrier polymer of either polyethylene oxide or poly(acrylic acid). The carrier polymer was extracted prior to MEA testing by a hot water soaking step. The resulting fibers were 15-17% porous, with a core-shell-like morphology (a coating of prima… Show more
“…The reason could be the presence of nmsized pores within the bers by the extraction of PAA carrier polymer-trapped water via capillary condensation, showing a similar voltage trend to PCL electrodes. 30 This suggests that although NFCL has different pore distributions from PCL, the difference in pore distribution did not inuence the cell performance as expected. It demonstrates a weak inuence of the nanober mat pore structure on performance, consistent with the conclusion drawn from LCD results.…”
“…The reason could be the presence of nmsized pores within the bers by the extraction of PAA carrier polymer-trapped water via capillary condensation, showing a similar voltage trend to PCL electrodes. 30 This suggests that although NFCL has different pore distributions from PCL, the difference in pore distribution did not inuence the cell performance as expected. It demonstrates a weak inuence of the nanober mat pore structure on performance, consistent with the conclusion drawn from LCD results.…”
“…The ethanolamine (MEA)s with Nafion in salt form (Na+, Li+, or Cs+ as sulfonic acid counterion) were prepared by Waldrop et al They showed little or no change in maximum power density when the relative humidity (RH) of the feed gas was lowered from 100% to 40%, while the eMEAwith H+-Nafion/peroxyacetic acid (PAA) fibers showed a 33% power loss at 40% RH. The higher power densities at low humidity were attributed to capillary condensation of water in porous fibers with a pore diameter of 1.25 nm or less [115]. On the one hand, the interconnected porous structure of nanofibers enables efficient gas diffusion and transport and provides uniform distribution of reactants and products within the fuel cell [110].…”
Electrospun porous carbon nanofiber mats have excellent properties, such as a large surface area, tunable porosity, and excellent electrical conductivity, and have attracted great attention in energy storage and power generation applications. Moreover, due to their exceptional properties, they can be used in dye-sensitized solar cells (DSSCs), membrane electrodes for fuel cells, catalytic applications such as oxygen reduction reactions (ORRs), hydrogen evolution reactions (HERs), and oxygen evolution reactions (OERs), and sensing applications such as biosensors, electrochemical sensors, and chemical sensors, providing a comprehensive insight into energy storage development and applications. This study focuses on the role of electrospun porous carbon nanofiber mats in improving energy storage and generation and contributes to a better understanding of the fabrication process of electrospun porous carbon nanofiber mats. In addition, a comprehensive review of various alternative preparation methods covering a wide range from natural polymers to synthetic carbon-rich materials is provided, along with insights into the current literature.
“…Another approach for generating new battery electrode architectures is nanofiber electrospinning. Over the last decade, fiber mat materials, where the fibers contain particles and a polymer binder, have been prepared and characterized for both fuel cell [24,25] and LIB [26][27][28][29] electrodes with promising results. Self et al, for example, showed that a freestanding nanofiber particle/polymer anode containing Si nanoparticles, poly(acrylic acid) and carbon black (Si/PAA/C) worked well in a Li battery coin cell [27].…”
Due to structural changes in silicon during lithiation/delithiation, most Li-ion battery anodes containing silicon show rapid gravimetric capacity fade upon charge/discharge cycling. Herein, we report on a new Si powder anode in the form of electrospun fibers with only poly(acrylic acid) (PAA) binder and no electrically conductive carbon. The performance of this anode was contrasted to a fiber mat composed of Si powder, PAA binder, and a small amount of carbon powder. Fiber mat electrodes were evaluated in half-cells with a Li metal counter/reference electrode. Without the addition of conductive carbon, a stable capacity of about 1500 mAh/g (normalized to the total weight of the anode) was obtained at 1C for 50 charge/discharge cycles when the areal loading of silicon was 0.30 mgSi/cm2, whereas a capacity of 800 mAh/g was obtained when the Si loading was increased to ~1.0 mgSi/cm2. On a Si weight basis, these capacities correspond to >3500 mAh/gSi. The capacities were significantly higher than those found with a slurry-cast powdered Si anode with PAA binder. There was no change in fiber anode performance (gravimetric capacity and constant capacity with cycling) when a small amount of electrically conductive carbon was added to the electrospun fiber anodes when the Si loading was ≤1.0 mgSi/cm2.
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