2022
DOI: 10.1016/j.apcatb.2022.121472
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Efficient FeCoNiCuPd thin-film electrocatalyst for alkaline oxygen and hydrogen evolution reactions

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Cited by 172 publications
(92 citation statements)
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“…The wettability of the obtained catalyst is indicated by the profile of the water drop (10 μL) on the material surface, and it is clearly seen that the contact angles (CA) of NF (Figure S17a) and Ni 3 S 2 /HPNF (Figure S17b) are all larger than 90°, indicating their hydrophobic property. On the contrary, the wettability of Pd 4 S-Ni 3 S 2 /HPNF (78.9°, Figure S17c) is significantly improved, and the more hydrophilic surface of the Pd 4 S-Ni 3 S 2 sample can lead to the formation of richer contact points near the reactive sites, , thereby improving the reaction kinetics of the HER process. The biphase, multidimensional morphologies of Pd 4 S-Ni 3 S 2 /HPNF obviously increase the surface reactive area, which can be indicated by the calculated C dl . As shown in Figure S18, the C dl of Pd 4 S-Ni 3 S 2 /HPNF is about 6.8 mF/cm 2 , and it is far bigger than for the NF ( C dl : 2.3 mF/cm 2 ), HPNF ( C dl : 2.6 mF/cm 2 ), and Ni 3 S 2 /HPNF ( C dl : 5.6 mF/cm 2 ) samples, manifesting that a higher HER performance is achieved for the Pd 4 S-Ni 3 S 2 /HPNF catalyst. The lower electrochemical impedance of Pd 4 S-Ni 3 S 2 /HPNF boosts the transfer rate of the electron in the electrocatalytic process, resulting in the observed high HER activity. The theory calculations confirm that the synergistic effect between the Pd 4 S and Ni 3 S 2 phases greatly decreases the Δ G H * , thus causing faster HER kinetics for water splitting. The in situ detecting technique discloses that the phase doping of Pd 4 S facilitates the water adsorption on the Pd site and weakens the S–H ads bond, thereby accelerating the HER kinetics for H 2 generation. …”
Section: Resultsmentioning
confidence: 99%
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“…The wettability of the obtained catalyst is indicated by the profile of the water drop (10 μL) on the material surface, and it is clearly seen that the contact angles (CA) of NF (Figure S17a) and Ni 3 S 2 /HPNF (Figure S17b) are all larger than 90°, indicating their hydrophobic property. On the contrary, the wettability of Pd 4 S-Ni 3 S 2 /HPNF (78.9°, Figure S17c) is significantly improved, and the more hydrophilic surface of the Pd 4 S-Ni 3 S 2 sample can lead to the formation of richer contact points near the reactive sites, , thereby improving the reaction kinetics of the HER process. The biphase, multidimensional morphologies of Pd 4 S-Ni 3 S 2 /HPNF obviously increase the surface reactive area, which can be indicated by the calculated C dl . As shown in Figure S18, the C dl of Pd 4 S-Ni 3 S 2 /HPNF is about 6.8 mF/cm 2 , and it is far bigger than for the NF ( C dl : 2.3 mF/cm 2 ), HPNF ( C dl : 2.6 mF/cm 2 ), and Ni 3 S 2 /HPNF ( C dl : 5.6 mF/cm 2 ) samples, manifesting that a higher HER performance is achieved for the Pd 4 S-Ni 3 S 2 /HPNF catalyst. The lower electrochemical impedance of Pd 4 S-Ni 3 S 2 /HPNF boosts the transfer rate of the electron in the electrocatalytic process, resulting in the observed high HER activity. The theory calculations confirm that the synergistic effect between the Pd 4 S and Ni 3 S 2 phases greatly decreases the Δ G H * , thus causing faster HER kinetics for water splitting. The in situ detecting technique discloses that the phase doping of Pd 4 S facilitates the water adsorption on the Pd site and weakens the S–H ads bond, thereby accelerating the HER kinetics for H 2 generation. …”
Section: Resultsmentioning
confidence: 99%
“…The wettability of the obtained catalyst is indicated by the profile of the water drop (10 μL) on the material surface, and it is clearly seen that the contact angles (CA) of NF (Figure S17a) and Ni 3 S 2 /HPNF (Figure S17b) are all larger than 90°, indicating their hydrophobic property. On the contrary, the wettability of Pd 4 S-Ni 3 S 2 /HPNF (78.9°, Figure S17c) is significantly improved, and the more hydrophilic surface of the Pd 4 S-Ni 3 S 2 sample can lead to the formation of richer contact points near the reactive sites, , thereby improving the reaction kinetics of the HER process.…”
Section: Resultsmentioning
confidence: 99%
“…[89] Similarly, Fang determined the PDOSs of each element to clarify the electronic structure of the FeCoNiCuPd shown in Figure 3g. [90] Last, but certainly not least, is the charge density difference, which helps understand the spatial distribution of electron density in the electrocatalyst structure. [91] Figure 3h is available for demonstrating the charge transfer due to the apparent electron depletion of Fe sites for the H 2 O adsorption, which was beneficial to the HER activity.…”
Section: Density Of States and Band Structurementioning
confidence: 99%
“…[ 21,25–28 ] The combinatorial properties of HEAs have been applied in catalysis and electrocatalysis. [ 21,29–40 ] The various types of HEA catalysts exhibit a synergistic effect to improve the HER performance greatly. [ 30–40 ] Determining the proper component and composition is the core of developing HEA catalysts.…”
Section: Introductionmentioning
confidence: 99%
“…[ 21,29–40 ] The various types of HEA catalysts exhibit a synergistic effect to improve the HER performance greatly. [ 30–40 ] Determining the proper component and composition is the core of developing HEA catalysts. Alloying of TMDs with various metal components can provide a platform for testing the benefits of HEA electrocatalysts.…”
Section: Introductionmentioning
confidence: 99%