Abstract:Radiation-grafted HDPE-based anion-exchange membranes perform better than LDPE-based benchmarks despite exhibiting similar ex situ properties.
“…[ 7 ] Varcoe and co‐workers reported that a HEMFC reaches a peak power density of 2.55 W cm −2 with an anodic metal loading of 0.6 mg PtRu cm −2 or 0.4 mg Pt cm −2 and a high‐density polyethylene‐(HDPE)‐based radiation‐grafted membrane. [ 8 ] It is obvious that the PtRu loading or Pt loading at the anode of HEMFCs is still high. For practical applications, the anodic noble metal loading has to be mitigated significantly.…”
A series of uniform 3.0–3.8 nm Pt1−xRux particles supported on nitrogen‐doped carbon (N‐C) is synthesized by wet‐impregnation, high‐temperature reduction, and high‐temperature NH3 etching. As far as it is known, the resultant Pt0.25Ru0.75/N‐C exhibits the highest activity toward alkaline hydrogen oxidation reaction (HOR) in terms of mass specific exchange current density (j0,m, 1654 A gPtRu−1), that is 4.7 and 1.4 times of commercial Pt/C (352 A gPt−1) and PtRu/C (1213 A gPtRu−1), respectively. The remarkable activity originates from a high electrochemical active surface area (ECSA), weakened hydrogen binding energy (HBE), and appropriate oxophilic property. Additionally, the Pt0.25Ru0.75/N‐C displays much improved durability during potential cycling with respect to commercial Pt/C and commercial PtRu/C, likely arising from the stabilizing effect of nitrogen dopant of N‐C on Pt0.25Ru0.75. Furthermore, the single cell fabricated with 0.08 mgPt cm−2 of the Pt0.25Ru0.75/N‐C as the anode reaches a peak power density of 831 mW cm−2, which is 1.8 and 1.1 times of that fabricated with 0.2 mgPt cm−2 of commercial Pt/C and 0.13 mgPt cm−2 of commercial PtRu/C as the anode, respectively. This study exhibits that low‐platinum alkaline HOR electrocatalyst should be a highly promising approach for hydroxide exchange membrane fuel cells (HEMFCs).
“…[ 7 ] Varcoe and co‐workers reported that a HEMFC reaches a peak power density of 2.55 W cm −2 with an anodic metal loading of 0.6 mg PtRu cm −2 or 0.4 mg Pt cm −2 and a high‐density polyethylene‐(HDPE)‐based radiation‐grafted membrane. [ 8 ] It is obvious that the PtRu loading or Pt loading at the anode of HEMFCs is still high. For practical applications, the anodic noble metal loading has to be mitigated significantly.…”
A series of uniform 3.0–3.8 nm Pt1−xRux particles supported on nitrogen‐doped carbon (N‐C) is synthesized by wet‐impregnation, high‐temperature reduction, and high‐temperature NH3 etching. As far as it is known, the resultant Pt0.25Ru0.75/N‐C exhibits the highest activity toward alkaline hydrogen oxidation reaction (HOR) in terms of mass specific exchange current density (j0,m, 1654 A gPtRu−1), that is 4.7 and 1.4 times of commercial Pt/C (352 A gPt−1) and PtRu/C (1213 A gPtRu−1), respectively. The remarkable activity originates from a high electrochemical active surface area (ECSA), weakened hydrogen binding energy (HBE), and appropriate oxophilic property. Additionally, the Pt0.25Ru0.75/N‐C displays much improved durability during potential cycling with respect to commercial Pt/C and commercial PtRu/C, likely arising from the stabilizing effect of nitrogen dopant of N‐C on Pt0.25Ru0.75. Furthermore, the single cell fabricated with 0.08 mgPt cm−2 of the Pt0.25Ru0.75/N‐C as the anode reaches a peak power density of 831 mW cm−2, which is 1.8 and 1.1 times of that fabricated with 0.2 mgPt cm−2 of commercial Pt/C and 0.13 mgPt cm−2 of commercial PtRu/C as the anode, respectively. This study exhibits that low‐platinum alkaline HOR electrocatalyst should be a highly promising approach for hydroxide exchange membrane fuel cells (HEMFCs).
“…Nonetheless, the highest AEMFC performances reported to date are based on this fabrication method. 3,22 DMD-10 shows a maximum power density of 800 mW cm À2 (compared to DMD-5 and DMD-3), which is likely a result of the thicker membrane, leading to increased ionic resistance (42 mOhm cm 2 @ 2000 mA cm À2 ) and an earlier onset of mass transport losses. The increased mass transport losses can most probably be ascribed to the reduced water back diffusion from the anode to the cathode side caused by the thicker membrane, 12,23 since all other fabrication and operation parameters were kept the same.…”
Section: Electrochemical Propertiesmentioning
confidence: 97%
“…8 The robustness to changes in relative humidity of the fuel cells described in this work is likely attributable to the very thin membranes, enabled by direct deposition: as motivated earlier, the use of very thin membranes is considered as key to access high performance, low power degradation as well as robust water balance between anode and cathode. 22,25 The best fuel cell performance was achieved at a relative humidity of 91/91% (68/68 C) with 1018 mW cm À2 . As shown in Fig.…”
Section: Electrochemical Propertiesmentioning
confidence: 99%
“…Nevertheless, the decay rates reported here, are still higher compared to the latest long-term tests for AEMFCs reporting average voltage decays of 0.068-0.4 mV h À1 and require further investigation. 4,22…”
Thin ionomer membranes are considered key to achieve high performances in anion exchange membrane fuel cells, as well as high performance robustness towards changes in relative humidity.
“…Later, a series of three AEMFCs were assembled with AEMs prepared with irradiated ETFE-based AEI (anion-exchange ionomer) powders with the QAs benzyl-N-methylpiperidinium (MPRD), benzyltrimethylammonium (TMA), and benzyl-N-methylpyrrolidinium (MPY) showing very good performances at 60 • C [107]. However, at the same time, a study with a new high-density polyethylene-based (HDPE) radiation-grafted AEM proved that using HDPE as a precursor film directly led to enhanced performance characteristics in comparison to an ETFE one [114]. Nevertheless, the longest durability testing of an AEMFC (H 2 /O 2 -fed) was reported by Omasta et al [115] using radiation grafted ETFE films bearing benzyltrimethylammonium (BTMA) cations as the AEM.…”
The use of ionizing radiation processing technologies has proven to be one of the most versatile ways to prepare a wide range of membranes with specific tailored functionalities, thus enabling them to be used in a variety of industrial, environmental, and biological applications. The general principle of this clean and environmental friendly technique is the use of various types of commercially available high-energy radiation sources, like 60Co, X-ray, and electron beam to initiate energy-controlled processes of free-radical polymerization or copolymerization, leading to the production of functionalized, flexible, structured membranes or to the incorporation of functional groups within a matrix composed by a low-cost polymer film. The present manuscript describes the state of the art of using ionizing radiation for the preparation and functionalization of polymer-based membranes for biomedical and environmental applications.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.