Abstract:Developing and designing highly active and robust catalysts for methanol oxidation reaction is imperative towards the commercialization process of direct methanol fuel cells. Herein, a Pt-Ni alloy catalyst (Pt1.5Ni-NGA) with...
“…25,26 According to the d-band theory, the transfer of an electron to Pt reduces its d-band center associated with Fermi energy levels, reducing the adsorption of toxic intermediates to the Pt active site during ethanol fuel oxidation, thus resulting in lower binding energy between Pt and the adsorbed toxic intermediate (e.g., CO), and the shi of the Pt binding energy to lower values decreases its d-band center, thus improving its catalytic performance for methanol oxidation. [27][28][29] The SEM images of the Pt/WO 3 electrode (Fig. S2 †) show that numerous tiny Pt/WO 3 particles constitute a 3D porous structure on the surface of the W matrix.…”
Section: Resultsmentioning
confidence: 99%
“…5f; Table S2 †). 26,29,[37][38][39][40][41][42][43][44][45][46][47][48][49][50] The Pt/WC 1−x /WO 3 electrode showed excellent catalytic performance not only in methanol aqueous solution, but also in ethylene glycol and propanetriol solutions (Fig. S11 †).…”
Section: Resultsmentioning
confidence: 99%
“…, CO), and the shift of the Pt binding energy to lower values decreases its d-band center, thus improving its catalytic performance for methanol oxidation. 27–29…”
The design of economical, efficient, and durable low-Pt catalysts is one of the directions in developing energy storage and conversion technologies. Herein, Pt/WC1-x/WO3 self-supported electrode with a low Pt-loading (17.4...
“…25,26 According to the d-band theory, the transfer of an electron to Pt reduces its d-band center associated with Fermi energy levels, reducing the adsorption of toxic intermediates to the Pt active site during ethanol fuel oxidation, thus resulting in lower binding energy between Pt and the adsorbed toxic intermediate (e.g., CO), and the shi of the Pt binding energy to lower values decreases its d-band center, thus improving its catalytic performance for methanol oxidation. [27][28][29] The SEM images of the Pt/WO 3 electrode (Fig. S2 †) show that numerous tiny Pt/WO 3 particles constitute a 3D porous structure on the surface of the W matrix.…”
Section: Resultsmentioning
confidence: 99%
“…5f; Table S2 †). 26,29,[37][38][39][40][41][42][43][44][45][46][47][48][49][50] The Pt/WC 1−x /WO 3 electrode showed excellent catalytic performance not only in methanol aqueous solution, but also in ethylene glycol and propanetriol solutions (Fig. S11 †).…”
Section: Resultsmentioning
confidence: 99%
“…, CO), and the shift of the Pt binding energy to lower values decreases its d-band center, thus improving its catalytic performance for methanol oxidation. 27–29…”
The design of economical, efficient, and durable low-Pt catalysts is one of the directions in developing energy storage and conversion technologies. Herein, Pt/WC1-x/WO3 self-supported electrode with a low Pt-loading (17.4...
“…4A-C). 25,26 Benefiting from the globular NCB embedded in the interspaces between carbon nanotubes, the Brunauer-Emmett-Teller (BET) specific surface area value of Pd/ NCB@NCNTs-2 was determined to be as high as 129.9 m 2 g −1 , which was larger than those of Pd/NCB (87.7 m 2 g −1 ) and Pd/ NCNTs (116.0 m 2 g −1 ), respectively. Moreover, the Barrett-Joyner-Halenda (BJH) pore size distribution curves further confirm the hierarchical porous structure with large mesopores and tiny macropores, as well as small mesopores and micropores for the as-prepared catalysts (Fig.…”
N-doped CNTs embedded with N-doped carbon black anchoring surface-clean Pd NCs exhibit exceptionally improved electrocatalytic behavior towards EOR, due to their unique 3D network architecture and abundant N-containing functional groups.
“…While noble metal-based electrocatalysts such as Pt and RuO 2 are acknowledged for their superior performance, their widespread application is limited by their scarcity and suboptimal activity. [9][10][11] To overcome these shortcomings, the design and synthesis of low Pt content catalysts with high catalytic performance have emerged as a primary strategy. Consequently, selecting support materials with strong electrochemical properties to effectively modulate the electronic properties of Pt through interface engineering, 12,13 construction of heterostructures, 14,15 and hybridization engineering 16 are promising approaches to enhance the catalytic activity of low precious metal content catalysts.…”
The potential of hydrogen production via water splitting technology makes it urgent to develop low-cost and highly active bifunctional catalysts for hydrogen and oxygen evolution reactions (HER/OER). In this study,...
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