2020
DOI: 10.1016/j.scib.2019.10.024
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A highly active and durable electrocatalyst for large current density hydrogen evolution reaction

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Cited by 69 publications
(42 citation statements)
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“…7f, g and S49). The volume-time curve for H 2 and O 2 is obtained by water drainage method at 0, 10,15,20,25,30,35,40,45, and 50 min measured at 30.0 mA. The volume-time curve for H 2 and O 2 is about 2:1, and they are close to the theoretical values, indicating the nearly 100% Faradic efficiency.…”
Section: Ws Catalytic Performancementioning
confidence: 62%
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“…7f, g and S49). The volume-time curve for H 2 and O 2 is obtained by water drainage method at 0, 10,15,20,25,30,35,40,45, and 50 min measured at 30.0 mA. The volume-time curve for H 2 and O 2 is about 2:1, and they are close to the theoretical values, indicating the nearly 100% Faradic efficiency.…”
Section: Ws Catalytic Performancementioning
confidence: 62%
“…on 3D porous substrate (e.g., NF) is significant, which can accelerate the mass transfer and bubbles escape during the electrochemical reaction process, and provide large specific surface area to expose abundant active sites [15,29]. MoS 2 /Ni 3 S 2 heterostructure nanowires selfsupported on NF were constructed by Cheng et al [30]. It exhibits a small overpotential of 182 mV at 500 mA cm −2 for HER, which is comparable to Pt/C.…”
Section: H O Cmentioning
confidence: 99%
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“…The one-step direct conversion of the mixed precursors via which different components are simultaneously generated and hybridized in situ represents the most straightforward and effective means to harvest heterostructures. 88 Recently, laser has been used to irradiate the mixed precursors for the construction of such structures ( Figure 7A). 89 Compared with the traditionally used methods, a laser-mediated process can significantly reduce the reaction time from many hours to several minutes and even seconds, suggesting an essentially improved efficiency.…”
Section: Laser-assisted Fabrication Of Heterostructuresmentioning
confidence: 99%
“…Stimulated by the development of alkaline exchange membranes [4], as well as highly efficient and stable platinum group materials (PGM)-free electrocatalysts for alkaline oxygen electrode reactions (oxygen reduction and oxygen evolution reactions) in the past decades [5,6], alkaline exchange membrane-based fuel cells (AEMFCs) and water electrolyzers (AEMWEs) have received considerable attentions as the alternatives to their proton exchange membrane-based counterparts [7,8]. However, the kinetics of HOR/HER in alkaline media, even for the PGM-based electrocatalysts, are over 100 times slower than those in acidic media [9][10][11][12]. More critically, despite considerable efforts have been devoted to investigating these two reversible reactions, the reason for the significantly kinetics-decreasing derived from the pH effect of electrolytes, as well as the mechanism for HOR/HER under alkaline media, still remain debatable [13][14][15][16][17][18].…”
Section: Introductionmentioning
confidence: 99%