过电位
塔菲尔方程
催化作用
化学
电催化剂
碳纳米管
钴
化学工程
电化学
黄铁矿
无机化学
吸附
物理化学
矿物学
有机化学
工程类
电极
作者
Di‐Yan Wang,Ming Gong,Hung-Lung Chou,Chun‐Jern Pan,Hsin‐An Chen,Yingpeng Wu,Meng‐Chang Lin,Mingyun Guan,Yang Jiang,Chun‐Wei Chen,Yuh‐Lin Wang,Bing‐Joe Hwang,Chia‐Chun Chen,Hongjie Dai
摘要
Hydrogen evolution reaction (HER) from water through electrocatalysis using cost-effective materials to replace precious Pt catalysts holds great promise for clean energy technologies. In this work we developed a highly active and stable catalyst containing Co doped earth abundant iron pyrite FeS2 nanosheets hybridized with carbon nanotubes (Fe1–xCoxS2/CNT hybrid catalysts) for HER in acidic solutions. The pyrite phase of Fe1–xCoxS2/CNT was characterized by powder X-ray diffraction and absorption spectroscopy. Electrochemical measurements showed a low overpotential of ∼0.12 V at 20 mA/cm2, small Tafel slope of ∼46 mV/decade, and long-term durability over 40 h of HER operation using bulk quantities of Fe0.9Co0.1S2/CNT hybrid catalysts at high loadings (∼7 mg/cm2). Density functional theory calculation revealed that the origin of high catalytic activity stemmed from a large reduction of the kinetic energy barrier of H atom adsorption on FeS2 surface upon Co doping in the iron pyrite structure. It is also found that the high HER catalytic activity of Fe0.9Co0.1S2 hinges on the hybridization with CNTs to impart strong heteroatomic interactions between CNT and Fe0.9Co0.1S2. This work produces the most active HER catalyst based on iron pyrite, suggesting a scalable, low cost, and highly efficient catalyst for hydrogen generation.
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