石墨烯
材料科学
过电位
催化作用
氧化物
纳米材料基催化剂
纳米颗粒
无机化学
拉曼光谱
X射线光电子能谱
杂原子
钌
可逆氢电极
化学工程
玻璃碳
氢
兴奋剂
碳纤维
纳米技术
电化学
电极
物理化学
有机化学
化学
循环伏安法
工作电极
冶金
复合材料
戒指(化学)
光学
光电子学
复合数
工程类
物理
作者
Laura Mallón,Javier Navarro‐Ruiz,Christian Cerezo-Navarrete,Nuria Romero,Iker Del Rosal,Jordi García‐Antón,Roger Bofill,Luis M. Martínez‐Prieto,Karine Philippot,Romuald Poteau,Xavier Sala
标识
DOI:10.1021/acsami.4c15547
摘要
Three different cathodic materials for the hydrogen evolution reaction (HER) consisting of Ru nanoparticles (NPs) supported onto a bare and two doped reduced graphene oxides (r-GO) have been studied. Ru NPs have been synthesized in situ by means of the organometallic approach in the presence of each reduced graphene support (bare (rGO), N-doped (NH2-rGO) and P-doped (P-rGO)). (HR)TEM, EDX, EA, ICP-OES, XPS, Raman and NMR techniques have been used to fully characterize the obtained rGO-supported Ru materials. These materials have been deposited onto a glassy carbon rotating disk electrode (GC-RDE) to assess their HER electrocatalytic activity at acidic pH. The results show that all three materials are stable under reductive conditions for at least 12 h, and that the heteroatom-doping of the graphene structure extremely increases the activity of the electrodes, especially for the case of Ru@P-rGO, where the overpotential at −10 mA·cm–2 decreases to only 2 mV. Realistic (based on experimental compositional data) modeling of the three rGO supports combined with DFT computational analysis of the electronic and electrocatalytic properties of the hybrid nanocatalysts allows attributing the observed electrocatalytic performances to a combination of interrelated factors such as the distance of the Ru atoms to the dopped rGO support and the hydride content at the Ru NP surface.
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