2023
DOI: 10.1016/j.apcatb.2022.122257
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Boosting borohydride oxidation by control lattice-strain of Ni@NiP electrocatalyst with core-shell structure

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Cited by 15 publications
(12 citation statements)
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“…The electrodeposition solution was composed of 1 M NiCl 2 ·6H 2 O and 0.1 M (NH 4 ) 2 SO 4 . Finally, a multi-potential step 24 was applied to prepare the Ni catalyst using an electrochemical station (CHI 660e, Shanghai Chen Hua Instrument Co. Ltd). Finally, the Ni catalyst was rinsed thoroughly with deionized water for standby.…”
Section: Methodsmentioning
confidence: 99%
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“…The electrodeposition solution was composed of 1 M NiCl 2 ·6H 2 O and 0.1 M (NH 4 ) 2 SO 4 . Finally, a multi-potential step 24 was applied to prepare the Ni catalyst using an electrochemical station (CHI 660e, Shanghai Chen Hua Instrument Co. Ltd). Finally, the Ni catalyst was rinsed thoroughly with deionized water for standby.…”
Section: Methodsmentioning
confidence: 99%
“…The details of the Rietveld refinement are the same as those in our previous work. 24 X-ray photoelectron spectroscopy (XPS) analysis was conducted using a Thermo Fisher Scientific ESCALAB250Xi instrument with Al Kα radiation, in order to investigate the surface composition of the catalysts. The C 1s peak at 284.8 eV, corresponding to the presence of surface adventitious carbon, was utilized as the calibration peak.…”
Section: Materials Characterizationmentioning
confidence: 99%
“…5c–f). To improve the nickel-based catalyst performance further, making it more valuable for applications, they introduced the P element and synthesized an efficient Ni@NiP catalyst 44 for BOR. The introduction of P inhibited the oxidation of metallic nickel, while introducing tensile lattice strain in the catalyst surface, which raised the D-band center of nickel and thus enhanced its BOR activity.…”
Section: Electrodesmentioning
confidence: 99%
“…= 10.6%) of the fuel used, excellent chemical stability for long-term operation, and mild operation conditions. In addition, using relatively less corrosive alkaline electrolytes offers the possibility of applying inexpensive, abundant transition metal catalysts, [44][45][46] which drives the commercialization of DBFCs. While using hydrogen peroxide instead of oxygen as an oxidant, DBFCs can attain a much higher open cell voltage (about 2.18 V) and significant theoretical energy density (17 kW h kg À1 ), 47,48 which are distinctly better than those of HCs (1.23 V and 3.28 kW h kg À1 ).…”
Section: Introductionmentioning
confidence: 99%
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