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  • Royal Society of Chemistry (RSC)  (2)
  • Tian, Zhong-Qun  (2)
  • Wang, Yanjie  (2)
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  • Royal Society of Chemistry (RSC)  (2)
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  • 1
    In: Chemical Science, Royal Society of Chemistry (RSC), Vol. 13, No. 19 ( 2022), p. 5639-5649
    Abstract: One of the most successful approaches for balancing the high stability and activity of water oxidation in alkaline solutions is to use amorphous and crystalline heterostructures. However, due to the lack of direct evidence at the molecular level, the nano/micro processes of amorphous and crystalline heterostructure electrocatalysts, including self-reconstruction and reaction pathways, remain unknown. Herein, the Leidenfrost effect assisted electrospray approach combined with phase separation was used for the first time to create amorphous NiO x /crystalline α-Fe 2 O 3 (a-NiO x /α-Fe 2 O 3 ) nanowire arrays. The results of in situ Raman spectroscopy demonstrate that with the increase of the potential at the a-NiO x /α-Fe 2 O 3 interface, a significant accumulation of OH can be observed. Combining with XAS spectra and DFT calculations, we believe that more OH adsorption on the Ni centers can facilitate Ni 2+ deprotonation to achieve the high-valence oxidation of Ni 4+ according to HSAB theory (Fe 3+ serves as a strong Lewis acid). This result promotes the electrocatalysts to follow the lattice oxygen activation mechanism. This work, for the first time, offers direct spectroscopic evidence for deepening the fundamental understanding of the Lewis acid effect of Fe 3+ , and reveals the synergistic effect on water oxidation via the unique amorphous and crystalline heterostructures.
    Type of Medium: Online Resource
    ISSN: 2041-6520 , 2041-6539
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2559110-1
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  • 2
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2021
    In:  Journal of Materials Chemistry A Vol. 9, No. 35 ( 2021), p. 20058-20067
    In: Journal of Materials Chemistry A, Royal Society of Chemistry (RSC), Vol. 9, No. 35 ( 2021), p. 20058-20067
    Abstract: NiFe (oxy)hydroxides (NiFeOOH) are considered as one of the most efficient electrocatalysts for water splitting. Although several strategies recently have been developed to fabricate NiFeOOH electrodes, such as electrodeposition, hydrothermal reaction, corrosion engineering, etc. , it has been a challenge to directly tune the energy level, conductivity and surface properties (such as molecular adsorption) of NiFeOOH with less time-consuming and convenient synthesis to overcome the relatively sluggish reaction kinetics. Herein, we, for the first time, utilize charged droplets to synthesize NiFeOOH with abundant oxygen vacancies (O v ) via the convenient electrospraying (ESI) approach without necessitating additional post-treatments. Specifically, the optimized NiFeOOH delivers much lower overpotentials of 145 mV, 215 mV and 360 mV for the hydrogen evolution reaction (HER), the oxygen evolution reaction (OER) and overall water splitting in 1 M KOH at 10 mA cm −2 with long-term durability over 180 h. The good performing electrocatalyst is much improved compared with the benchmark Pt/C/NF in the high current density region, RuO 2 /NF and other NiFe-based electrocatalysts. Simultaneously, the unique reaction environment of the droplet (confinement, superacid and desolvation) was further explored to understand the synthesis reaction acceleration process and related oxygen defect formation mechanisms. Also, we used density functional theory (DFT) to investigate the change of free energy of the reaction pathway caused by oxygen vacancies and understand the reaction mechanism of electrocatalysts prepared by different treatment methods. The calculation results show that the shortened Fe–O bonds and oxygen defects of NiFeOOH synergistically improve the interaction between the metal cations and the intermediate species and further accelerate the overall reaction kinetics. This work demonstrates that the charged microdroplet chemistry offers a novel means to expedite the design of powerful electrocatalysts.
    Type of Medium: Online Resource
    ISSN: 2050-7488 , 2050-7496
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2021
    detail.hit.zdb_id: 2702232-8
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