“…4(b) and (d) on KB. Because the reported sizes of Pt catalysts synthesized in the liquid phase 32,45 are similar to or larger than the size in this study, the results indicate that the DiPET method enables us to fabricate a smaller Pt catalyst on carbon material supports.…”
Section: Tem Observation Of Pt Ncssupporting
confidence: 61%
“…Pt NPs were loaded on MC or KB in liquid phase synthesis under a wet process. As previously reported, 32,33,45 an aqueous solution of chloroplatinic acid and citric acid was added and mixed in an aqueous solvent in which powders of MC or KB were dispersed, and the mixed solution was nally reduced with sodium borohydride to grow Pt NPs on the surface of MC or KB. Aer the supernatant solution was removed by centrifugation, the precipitation products composed of Pt particles on MC(Pt-NP(w)/MC) or KB(Pt-NP(w)/KB) were further used to fabricate the electrode.…”
Section: Pt Np Loading On MC or Kbmentioning
confidence: 99%
“…The working electrodes were prepared using four types of Pt-NC(d)/MC, Pt-NC(d)/KB, Pt-NP(w)/MC, and Pt-NP(w)/KB. 32,33,45 First, catalyst inks were prepared by mixing 18.5 mg of the carbon-supported catalysts with 19 mL of deionized water, 6.0 mL of 2-propanol, and diluted ionomer (5 wt% Naon) solution. The amount of Naon solution was 33 and 100 mL for Pt-NC(NP)/MC and Pt-NC(NP)/KB, respectively.…”
Section: Electrochemical Measurementsmentioning
confidence: 99%
“…In the evaluation of cell performance using the fabricated MEAs, current and voltage (I-V) measurements were performed for PEFCs. The I-V measurements were performed at a cell temperature of 80 C. Humidied hydrogen gas (200 mL min À1 , 100% relative humidity (RH) at 80 C) and humidied air (200 mL min À1 , 100% RH at 70 C) were supplied to the anode and cathode, respectively, 45 and gas utilization is approximately 70% at the anode and 40% at the cathode. 4(a)-(d).…”
Section: Mea Preparation and Cell Performance Measurementmentioning
confidence: 99%
“…For MC, the immobilization site is an edge of stacked graphene sheets, where carbon nanolaments of MC grow radially from diamond oxide in a stacked cup shape. 32,45 The stacked graphene edges appear to exhibit high selectivity for immobilizing Pt catalysts. For KB, in contrast, the immobilization sites of the mainly hexagonal structure of the graphite surface on KB 23 is not as active as the edge of the stacked graphene in MC, because KB has a porous carbon structure.…”
The development of efficient fuel cells greatly promotes reducing the consumption of fossil energy, and it is crucial to enhance the platinum (Pt) catalytic activity by optimizing both the nanoparticle size and support effect.
“…4(b) and (d) on KB. Because the reported sizes of Pt catalysts synthesized in the liquid phase 32,45 are similar to or larger than the size in this study, the results indicate that the DiPET method enables us to fabricate a smaller Pt catalyst on carbon material supports.…”
Section: Tem Observation Of Pt Ncssupporting
confidence: 61%
“…Pt NPs were loaded on MC or KB in liquid phase synthesis under a wet process. As previously reported, 32,33,45 an aqueous solution of chloroplatinic acid and citric acid was added and mixed in an aqueous solvent in which powders of MC or KB were dispersed, and the mixed solution was nally reduced with sodium borohydride to grow Pt NPs on the surface of MC or KB. Aer the supernatant solution was removed by centrifugation, the precipitation products composed of Pt particles on MC(Pt-NP(w)/MC) or KB(Pt-NP(w)/KB) were further used to fabricate the electrode.…”
Section: Pt Np Loading On MC or Kbmentioning
confidence: 99%
“…The working electrodes were prepared using four types of Pt-NC(d)/MC, Pt-NC(d)/KB, Pt-NP(w)/MC, and Pt-NP(w)/KB. 32,33,45 First, catalyst inks were prepared by mixing 18.5 mg of the carbon-supported catalysts with 19 mL of deionized water, 6.0 mL of 2-propanol, and diluted ionomer (5 wt% Naon) solution. The amount of Naon solution was 33 and 100 mL for Pt-NC(NP)/MC and Pt-NC(NP)/KB, respectively.…”
Section: Electrochemical Measurementsmentioning
confidence: 99%
“…In the evaluation of cell performance using the fabricated MEAs, current and voltage (I-V) measurements were performed for PEFCs. The I-V measurements were performed at a cell temperature of 80 C. Humidied hydrogen gas (200 mL min À1 , 100% relative humidity (RH) at 80 C) and humidied air (200 mL min À1 , 100% RH at 70 C) were supplied to the anode and cathode, respectively, 45 and gas utilization is approximately 70% at the anode and 40% at the cathode. 4(a)-(d).…”
Section: Mea Preparation and Cell Performance Measurementmentioning
confidence: 99%
“…For MC, the immobilization site is an edge of stacked graphene sheets, where carbon nanolaments of MC grow radially from diamond oxide in a stacked cup shape. 32,45 The stacked graphene edges appear to exhibit high selectivity for immobilizing Pt catalysts. For KB, in contrast, the immobilization sites of the mainly hexagonal structure of the graphite surface on KB 23 is not as active as the edge of the stacked graphene in MC, because KB has a porous carbon structure.…”
The development of efficient fuel cells greatly promotes reducing the consumption of fossil energy, and it is crucial to enhance the platinum (Pt) catalytic activity by optimizing both the nanoparticle size and support effect.
We prepared and investigated the composites of the spinel Li 4 Ti 5 O 12 (LTO) and Marimocarbon (MC) by the hydrothermal method that could form uniform electric paths without aggregation of the LTO particles for high capacity and high rate lithium-ion batteries. MC consisted of many fine carbon nanofilaments (CNFs) intertwined with each other in a complicated fashion. There are vacant space volumes of hundred nanometers between the CNFs. LTO particles were deposited in the space volumes among the tangled CNFs of the MCs. LTO is one of the most attractive anode materials for lithium-ion batteries because of its structural stability and safety. The morphology, microstructure and elemental composition of the LTO/MC composites were characterized by scanning electron microscopy (SEM), and X-ray diffraction (XRD). A charge-discharge test revealed that the LTO/MC composite (MC 10 wt%, prepared using a fluidized bed flow-reactor) produced the specific capacity of 170 mA g -1 at 1C (1C = 175 mA g -1 ). The LTO/MC composite maintained the specific capacity of 47 mAh g -1 even in the high rate zone at 30C whereas only the pristine LTO the produced 15 mAh g -1 at this rate. The unique structure of the LTO/MC composites can contribute to improving the electrochemical performance of the LTO anode. The LTO/MC composites can provide an effective approach to improve the lithium-ion battery performances.
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