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  • Royal Society of Chemistry (RSC)  (2)
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  • Royal Society of Chemistry (RSC)  (2)
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  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2021
    In:  Materials Chemistry Frontiers Vol. 5, No. 22 ( 2021), p. 8047-8055
    In: Materials Chemistry Frontiers, Royal Society of Chemistry (RSC), Vol. 5, No. 22 ( 2021), p. 8047-8055
    Abstract: Developing cost-effective Ir-based anode catalysts for proton exchange membrane (PEM) water electrolysis has been recognized as an efficient and pragmatic approach; however, many challenges remain to lower the Ir content while maintaining high electrocatalytic performance. Herein, an effective strategy of tailoring IrO 2 @TiN 1+ x nano-heterojunctions by defects is reported, aiming at enhancing the intrinsic oxygen evolution reaction (OER) activity of IrO 2 at a low Ir amount. A remarkable OER activity in an acidic solution is achieved for IrO 2 @TiN 1+ x with 7.3 times of mass activity and 1.8 times of specific activity relative to IrO 2 . As the anode electrode in a PEM single cell, IrO 2 @TiN 1+ x also reveals the optimal activity with 1.916 V at 2 A cm −2 , which is 57 mV and 130 mV lower than that of IrO 2 @TiN and IrO 2 , respectively. Meantime, the IrO 2 @TiN 1+ x electrode manifests good stability at 1 A cm −2 for 100 h. Electrochemical characterization analysis and DFT calculation results indicate that the increase in the number of active sites and the modulating electronic interaction between IrO 2 and TiN 1+ x could multiply the active sites and accelerate the OER kinetics of IrO 2 . Thus, the IrO 2 @TiN 1+ x nano-heterostructure reveals superior electrocatalytic performance and good stability at a low Ir content.
    Type of Medium: Online Resource
    ISSN: 2052-1537
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2021
    detail.hit.zdb_id: 2867881-3
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  • 2
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Journal of Materials Chemistry A Vol. 10, No. 31 ( 2022), p. 16524-16532
    In: Journal of Materials Chemistry A, Royal Society of Chemistry (RSC), Vol. 10, No. 31 ( 2022), p. 16524-16532
    Abstract: To alleviate energy and environmental issues, photocatalytic nitrogen fixation to ammonia is a promising technique compared to the conventional Haber–Bosch process. In the present work, a CdS/TpPa-1 heterojunction was constructed by the in situ formation of ultrafine CdS nanoparticles in the TpPa-1-COF matrix. The NH 3 production rates over the as-obtained CdS/TpPa-1 samples with different contents of CdS were optimized, and the highest rate was up to 241 μmol g −1 h −1 under visible light in the absence of sacrificial agents and cocatalysts, which was 3.0 and 1.7 times that of pure CdS and TpPa-1. The isotope labeled 15 N 2 gas was used as the nitrogen source for photocatalytic nitrogen fixation to clarify the source of nitrogen in ammonia, and the result indicated that the nitrogen source for ammonia was N 2 gas. The charge transfer mechanism of CdS/TpPa-1 was consistent with that of the type II heterojunction, which was verified by in situ X-ray photoelectron spectroscopy (XPS). Besides, the reaction mechanism of N 2 to NH 3 was analyzed by in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and density functional theory (DFT) calculations, and the alternating mechanism was energetically more likely to occur than the distal mechanism. This work may provide a valuable route to construct COF-based heterojunctions for efficient photocatalytic N 2 fixation.
    Type of Medium: Online Resource
    ISSN: 2050-7488 , 2050-7496
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2702232-8
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