热重分析
化学
乙二醇
催化作用
过电位
X射线光电子能谱
甲醇
热稳定性
傅里叶变换红外光谱
化学工程
无机化学
电化学
有机化学
电极
物理化学
工程类
作者
Samanka Narayan Bhaduri,Debojit Ghosh,Rupak Chatterjee,Samarpita Das,Indrani Pramanick,Asim Bhaumik,Papu Biswas
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-08-01
卷期号:62 (32): 12832-12842
被引量:2
标识
DOI:10.1021/acs.inorgchem.3c01479
摘要
Methanol oxidation reaction (MOR) is a perfect alternative to the conventional oxygen evolution reaction (OER), generally utilized as the anode reaction for hydrogen generation via the electrochemical water splitting method. Moreover, MOR is also relevant to direct methanol fuel cells (DMFCs). These facts motivate the researchers to develop economical and efficient electrocatalysts for MOR. Herein, we have introduced an ethylene glycol-linked tetraphenyl porphyrin-based (EG-POR) covalent organic polymer (COP). The Ni(II)-incorporated EG-POR material Ni-EG-POR displayed excellent OER and MOR activities in an alkaline medium. The materials were thoroughly characterized using 13C solid-state NMR, Fourier transform infrared spectroscopy (FT-IR), Brunauer–Emmett–Teller (BET) surface area analyzer, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), thermogravimetric analyzer (TGA), and powder X-ray diffraction (PXRD) techniques. These organic–inorganic hybrid materials showed high chemical and thermal stability. Ni-EG-POR requires an overpotential of 400 mV (vs RHE) in OER and 190 mV (vs RHE) in MOR to achieve a current density of 10 mA cm–2. In addition, the catalyst also showed excellent chronoamperometric and chronopotentiometric stability, indicating that the catalyst can provide stable current over a longer period and its potential as a non-noble metal MOR catalyst.
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