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通过脉冲电流从瓦特镀液和柠檬酸盐镀液中电沉积获得的镍电催化剂,用于增强碱性介质中的析氢反应。

Nickel Electrocatalysts Obtained by Pulsed Current Electrodeposition from Watts and Citrate Baths for Enhanced Hydrogen Evolution Reaction in Alkaline Media.

作者信息

Bojîncă Raluca, Muntean Roxana, Crişan Rebeca, Kellenberger Andrea

机构信息

Faculty of Chemical Engineering, Biotechnologies and Environmental Protection, Politehnica University Timişoara, Piata Victoriei No. 2, 300006 Timişoara, Romania.

Department of Materials and Manufacturing Engineering, Politehnica University Timișoara, Piata Victoriei No. 2, 300006 Timişoara, Romania.

出版信息

Materials (Basel). 2025 Jun 12;18(12):2775. doi: 10.3390/ma18122775.

Abstract

Efficient and low-cost electrocatalysts for the hydrogen evolution reaction (HER) in alkaline media are essential for sustainable hydrogen production. In this study, Ni electrocatalysts were deposited on pencil graphite using a simple one-step pulsed current electrodeposition method, from both acidic Watts and alkaline citrate baths. The influence of bath type and electrodeposition parameters-current density and temperature-on catalyst morphology and performance for HER was systematically investigated by scanning electron microscopy and electrochemical methods. Linear sweep voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy (EIS) were used to evaluate the electrocatalytic activity, stability, and HER mechanism. The best catalytic performance was achieved for the Ni electrocatalyst deposited from the citrate bath at 50 mA cm and 40 °C, showing an exchange current density of 0.93 mA cm, a Tafel slope of -208 mV dec, and overpotentials of -210 mV and -386 mV at 10 and 100 mA cm, respectively, in 1 M KOH solution. Chronopotentiometry confirmed improved stability and an overpotential reduction of approximately 92 mV as compared to pure Ni, while EIS revealed the lowest charge transfer resistance. It was shown that the electrocatalysts deposited from the citrate bath outperform those from the Watts bath, and electrodeposition at 40 °C is optimal for achieving the highest electrocatalytic activity for HER.

摘要

用于碱性介质中析氢反应(HER)的高效低成本电催化剂对于可持续制氢至关重要。在本研究中,采用简单的一步脉冲电流电沉积法,从酸性瓦特镀液和碱性柠檬酸盐镀液中,将镍电催化剂沉积在铅笔石墨上。通过扫描电子显微镜和电化学方法,系统研究了镀液类型和电沉积参数(电流密度和温度)对HER催化剂形态和性能的影响。采用线性扫描伏安法、计时电位法和电化学阻抗谱(EIS)来评估电催化活性、稳定性和HER机理。在50 mA cm²和40 °C条件下从柠檬酸盐镀液中沉积的镍电催化剂表现出最佳催化性能,在1 M KOH溶液中,其交换电流密度为0.93 mA cm²,塔菲尔斜率为-208 mV dec⁻¹,在10和100 mA cm²时的过电位分别为-210 mV和-386 mV。计时电位法证实与纯镍相比稳定性有所提高,过电位降低了约92 mV,而EIS显示电荷转移电阻最低。结果表明,从柠檬酸盐镀液中沉积的电催化剂优于从瓦特镀液中沉积的电催化剂,并且在40 °C下进行电沉积对于实现HER的最高电催化活性最为理想。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9669/12195463/969ad0bdbee8/materials-18-02775-g001.jpg

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