3 research outputs found

    Photoresponse of a Single Y‑Junction Carbon Nanotube

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    We report investigation of optical response in a single strand of a branched carbon nanotube (CNT), a Y-junction CNT composed of multiwalled CNTs. The experiment was performed by connecting a pair of branches while grounding the remaining one. Of the three branch combinations, only one combination is optically active which also shows a nonlinear semiconductor-like <i>I</i>–<i>V</i> curve, while the other two branch combinations are optically inactive and show linear ohmic <i>I</i>–<i>V</i> curves. The photoresponse includes a zero-bias photocurrent from the active branch combination. Responsivity of ≈1.6 mA/W has been observed from a single Y-CNT at a moderate bias of 150 mV with an illumination of wavelength 488 nm. The photoresponse experiment allows us to understand the nature of internal connections in the Y-CNT. Analysis of data locates the region of photoactivity at the junction of only two branches and only the combination of these two branches (and not individual branches) exhibits photoresponse upon illumination. A model calculation based on back-to-back Schottky-type junctions at the branch connection explains the <i>I</i>–<i>V</i> data in the dark and shows that under illumination the barriers at the contacts become lowered due to the presence of photogenerated carriers

    Solution-Processed CoFe<sub>2</sub>O<sub>4</sub> Nanoparticles on 3D Carbon Fiber Papers for Durable Oxygen Evolution Reaction

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    We report CoFe<sub>2</sub>O<sub>4</sub> nanoparticles (NPs) synthesized using a facile hydrothermal growth and their attachment on 3D carbon fiber papers (CFPs) for efficient and durable oxygen evolution reaction (OER). The CFPs covered with CoFe<sub>2</sub>O<sub>4</sub> NPs show orders of magnitude higher OER performance than bare CFP due to high activity of CoFe<sub>2</sub>O<sub>4</sub> NPs, leading to a small overpotential of 378 mV to get a current density of 10 mA/cm<sup>2</sup>. Significantly, the CoFe<sub>2</sub>O<sub>4</sub> NPs-on-CFP electrodes exhibit remarkably long stability evaluated by continuous cycling (over 15 h) and operation with a high current density at a fixed potential (over 40 h) without any morphological change and with preservation of all materials within the electrode. Furthermore, the CoFe<sub>2</sub>O<sub>4</sub> NPs-on-CFP electrodes also exhibit hydrogen evolution reaction (HER) performance, which is considerably higher than that of bare CFP, acting as a bifunctional electrocatalyst. The achieved results show promising potential for efficient, cost-effective, and durable hydrogen generation at large scales using earth-abundant materials and cheap fabrication processes

    Solution-Processed CoFe<sub>2</sub>O<sub>4</sub> Nanoparticles on 3D Carbon Fiber Papers for Durable Oxygen Evolution Reaction

    No full text
    We report CoFe<sub>2</sub>O<sub>4</sub> nanoparticles (NPs) synthesized using a facile hydrothermal growth and their attachment on 3D carbon fiber papers (CFPs) for efficient and durable oxygen evolution reaction (OER). The CFPs covered with CoFe<sub>2</sub>O<sub>4</sub> NPs show orders of magnitude higher OER performance than bare CFP due to high activity of CoFe<sub>2</sub>O<sub>4</sub> NPs, leading to a small overpotential of 378 mV to get a current density of 10 mA/cm<sup>2</sup>. Significantly, the CoFe<sub>2</sub>O<sub>4</sub> NPs-on-CFP electrodes exhibit remarkably long stability evaluated by continuous cycling (over 15 h) and operation with a high current density at a fixed potential (over 40 h) without any morphological change and with preservation of all materials within the electrode. Furthermore, the CoFe<sub>2</sub>O<sub>4</sub> NPs-on-CFP electrodes also exhibit hydrogen evolution reaction (HER) performance, which is considerably higher than that of bare CFP, acting as a bifunctional electrocatalyst. The achieved results show promising potential for efficient, cost-effective, and durable hydrogen generation at large scales using earth-abundant materials and cheap fabrication processes
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