电催化剂
电化学
石墨烯
联氨(抗抑郁剂)
催化作用
碳纳米管
氧化物
材料科学
X射线光电子能谱
杂原子
化学
无机化学
电极
化学工程
纳米技术
有机化学
物理化学
戒指(化学)
工程类
色谱法
作者
Parag P. Chavan,Vijay S. Sapner,Bhaskar R. Sathe
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2022-04-18
卷期号:36 (9): 4799-4806
被引量:11
标识
DOI:10.1021/acs.energyfuels.2c00676
摘要
One of the most essential processes in industrial and other potential energy applications is the electrochemical hydrazine oxidation reaction (HzOR). With an onset potential of 0.75 V versus reversible hydrogen electrode (RHE), the electrochemical HzOR performance of histidine-functionalized graphene oxide (Hist@rGO) is substantially enhanced with an achieved higher current of 24 mA/cm2 at 1.95 V versus RHE in 0.5 M KOH. Hist@rGO has the highest electrocatalytic performance for hydrazine oxidation processes according to electrochemical measurements. Moreover, the Hist@rGO-supported material performs admirably that may be attributed to its synergistic catalytic activity. The presence of an imidazole ring containing heteroatoms on the top of GO boosts the electrocatalytic activity and electron-transfer capacities toward the HzOR, resulting in outstanding electrochemical HzOR performance for the Hist@rGO electrocatalyst. The size of Hist@rGO is confirmed by morphological studies using high-resolution transmission electron microscopy. From the binding energies of C–N, C–O, and C–C signals, X-ray photoelectron spectroscopy validates the surface modification of GO by histidine (Hist@rGO). According to our data, the metal-free amino acid-functionalized carbon-based electrocatalyst has an excellent electrochemical HzOR performance and plays an important role in activity.
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