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  • Royal Society of Chemistry (RSC)  (2)
  • Wu, Jie  (2)
  • Yang, Hao  (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) ; 2023
    In:  Journal of Materials Chemistry A Vol. 11, No. 8 ( 2023), p. 4037-4044
    In: Journal of Materials Chemistry A, Royal Society of Chemistry (RSC), Vol. 11, No. 8 ( 2023), p. 4037-4044
    Abstract: Rational tailoring of highly efficient nanocatalysts is the ultimate goal of catalysis research, in which strain-engineering provides an effective method to tune the electronic structure of electrocatalysts. However, it remains difficult to clarify a definite relationship between reactivity and the strain effect due to the complicated ligand effect and synergistic effect in a multi-metal-element system. Here, porous flexible iridium nanosheets (Ir-PFNSs) with tunable compressive strain (ranging from 0 to −9.0%) were successfully obtained by directly annealing metastable 3R phase iridium oxide nanosheets in a hydrogen atmosphere, providing an ideal model electrocatalyst for studying the correlation between reactivity and lattice strain. The electrochemical results show that optimal Ir-PFNSs-300 may deliver an ultra-low overpotential of 18 mV at a current density of −10 mA cm geo −2 with a Tafel slope of 19.5 mV dec −1 for the hydrogen evolution reaction (HER). Density functional theory (DFT) calculations indicate that iridium nanosheets with tunable compressive strain trigger a new three-hydrogen pathway for the HER. This work successfully establishes a definite correlation between reactivity and lattice strain.
    Type of Medium: Online Resource
    ISSN: 2050-7488 , 2050-7496
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2702232-8
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  • 2
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2023
    In:  Energy & Environmental Science Vol. 16, No. 8 ( 2023), p. 3526-3533
    In: Energy & Environmental Science, Royal Society of Chemistry (RSC), Vol. 16, No. 8 ( 2023), p. 3526-3533
    Abstract: The two-electron oxygen reduction reaction (2e − ORR) in neutral media is a promising method to achieve hydrogen peroxide (H 2 O 2 ) from oxygen (O 2 ) directly in a sustainable way. Here, we show an ideal ZnO@ZnO 2 electrocatalyst for efficient O 2 reduction to H 2 O 2 in a neutral medium. The in situ growth of ZnO 2 on ZnO forms the operation active sites, namely the heterogeneous interface between tetrahedral ZnO and octahedral ZnO 2 , weakening the binding energies of both OOH* and O*. In a 0.1 M K 2 SO 4 electrolyte, ZnO@ZnO 2 shows a H 2 O 2 selectivity of nearly 100.0% via the ORR, while it can convert O 2 to H 2 O 2 with a production rate of 5.47 mol g cat −1 h −1 at 0.1 V vs. RHE and a Faraday efficiency (FE) of ∼95.5%, tested using a gas diffusion electrode device. The pulse voltage-induced current (PVC) was utilized in conjunction with a number of in situ characterization techniques and electrochemical studies to disclose the transformation of the ZnO surface and the production process of operational catalytic active sites on ZnO.
    Type of Medium: Online Resource
    ISSN: 1754-5692 , 1754-5706
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2439879-2
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