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从{Fe(NO)}-还原二亚硝酰基铁配合物开始的电催化水还原:将氮掺杂的FeO(OH)鉴定为真正的多相催化剂。

Electrocatalytic Water Reduction Beginning with a {Fe(NO)}-Reduced Dinitrosyliron Complex: Identification of Nitrogen-Doped FeO (OH) as a Real Heterogeneous Catalyst.

作者信息

Ke Chun-Hung, Shih Wei-Chih, Tsai Fu-Te, Tsai Ming-Li, Ching Wei-Min, Hsieh Hung-Hsi, Liaw Wen-Feng

机构信息

Department of Chemistry and Frontier Research Center of Fundamental and Applied Science of Matters , National Tsing Hua University , Hsinchu 30013 , Taiwan.

Department of Chemistry , National Sun Yat-sen University , Kaohsiung 80424 , Taiwan.

出版信息

Inorg Chem. 2018 Dec 3;57(23):14715-14726. doi: 10.1021/acs.inorgchem.8b02451. Epub 2018 Nov 19.

Abstract

Electron paramagnetic resonance, IR, single-crystal X-ray diffraction, and density functional theory computation reveal that the electronic structure of α-diimine-coordinated {Fe(NO)}-reduced dinitrosyliron complexes (DNICs) may best be described as [{Fe(NO)}-L], with the added electron residing mainly on the α-diimine ligand framework. The combination of electrochemistry, gas chromatography, Fourier transform infrared, X-ray photoelectron spectroscopy, and scanning electron microscopy-energy-dispersive X-ray studies demonstrates that the cathodic potential promotes/triggers the transformation of an α-diimine-coordinated {Fe(NO)}-reduced DNIC into a particulate deposit on the electrode, and electrodeposited-film electrodes, CFeO and CFeNO, are kinetically dominant electrocatalysts responsible for hydrogen evolution reaction (HER) from water with quantitative Faradaic efficiency. In comparison with the CFeO electrode reaching a current density of 10 mA/cm with an overpotential of 333 mV for HER, the nitrogen-doped iron oxide electrode, CFeNO, requires 147 mV of overpotential to achieve a current density of 10 mA/cm in a 1 M NaOH aqueous solution. The CFeNO electrode exhibits higher kinetic efficiency (Tafel slope of 59 mV/dec) than the CFeO electrode (Tafel slope of 122 mV/dec) in alkaline conditions. As opposed to high R (74.3 Ω) displayed by the CFeO electrode, the smaller charge-transfer resistance ( R) of the CFeNO electrode (34.0 Ω) demonstrated that the better HER catalytic activity may be ascribed to the incorporation of nitrogen into iron oxide architecture, which increases the surface roughness and electroconductivity of the CFeNO electrode (56.9% iron content and nitrogen electron-donating effect) and improves HER catalysis by polarizing the incoming water molecule (acting as a proton tray). This result implicates that a (NH)SO-assisted nitrogen-doping strategy is a direct and effective method to realize synergistic regulation of the reaction dynamics, catalytically active sites and electronic conductivity, endowing this nitrogen-doped material CFeNO electrode as a promising HER electrocatalyst under alkaline conditions.

摘要

电子顺磁共振、红外光谱、单晶X射线衍射和密度泛函理论计算表明,α-二亚胺配位的{Fe(NO)}-还原二亚硝酰基铁配合物(DNICs)的电子结构最好描述为[{Fe(NO)}-L],额外的电子主要位于α-二亚胺配体骨架上。电化学、气相色谱、傅里叶变换红外光谱、X射线光电子能谱和扫描电子显微镜-能量色散X射线研究的结合表明,阴极电位促进/触发了α-二亚胺配位的{Fe(NO)}-还原DNIC向电极上颗粒沉积物的转变,并且电沉积膜电极CFeO和CFeNO是动力学上占主导的电催化剂,负责以定量的法拉第效率从水中析氢反应(HER)。与CFeO电极相比,CFeO电极在HER时过电位为333 mV时达到电流密度10 mA/cm²,而氮掺杂的铁氧化物电极CFeNO在1 M NaOH水溶液中需要147 mV的过电位才能达到10 mA/cm²的电流密度。在碱性条件下,CFeNO电极比CFeO电极表现出更高的动力学效率(塔菲尔斜率为59 mV/dec)(CFeO电极的塔菲尔斜率为122 mV/dec)。与CFeO电极显示的高电阻(74.3 Ω)相反,CFeNO电极较小的电荷转移电阻(R)(34.0 Ω)表明,更好的HER催化活性可能归因于氮掺入铁氧化物结构中,这增加了CFeNO电极的表面粗糙度和电导率(铁含量为56.9%以及氮的给电子效应),并通过极化进入的水分子(充当质子托盘)改善HER催化作用。该结果表明,(NH)SO辅助的氮掺杂策略是实现反应动力学、催化活性位点和电子电导率协同调节的直接有效方法,使这种氮掺杂材料CFeNO电极成为碱性条件下有前景的HER电催化剂。

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