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氧化鈰-鎳鎢復(fù)合電極的制備及其析氫催化性能
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西北有色金屬研究院

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陜西省重點(diǎn)研發(fā)計(jì)劃(項(xiàng)目號(hào)2021GY-210)


Preparation of cerium oxide Ni-W composite electrode and its Catalytic performance for hydrogen evolution reaction
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    摘要:

    以70um厚的Ni-6W合金薄帶為基體,采用陽極氧化法制備納米多孔NiW后,再化學(xué)溶液沉積CeO2制備Ni和CeO2 (200)晶面暴露的納米多孔NiW-CeO2電極。采用掃描電鏡(SEM)、X射線衍射(XRD)和XPS對(duì)電極形貌和表面結(jié)構(gòu)進(jìn)行表征。通過陰極極化曲線、循環(huán)伏安曲線和電化學(xué)阻抗技術(shù)表征各電極的電解析氫行為。結(jié)果表明(200)晶面暴露的納米多孔NiW-CeO2電極比Ni(111)晶面暴露的Ni-CeO2電極和無擇優(yōu)取向的Ni-S-CeO2和Ni-Zn-CeO2電極的析氫性能好。該復(fù)合電極具有比文獻(xiàn)中所報(bào)道的共沉積的Ni-CeO2更高的交換電流密度1.7×10-1A cm-2。在1M NaOH溶液中達(dá)到100 mA cm-2電流密度時(shí),過電位比NiW-CeO2電極和NiW電極分別降低了分別降低55mV和81mV。對(duì)CeO2加入后對(duì)整個(gè)析氫過程的電化學(xué)過程的影響進(jìn)行了分析。本文通過該合成方法來控制CeO2的形貌,繼而選擇性暴露(200)晶面,實(shí)現(xiàn)對(duì)NiW-CeO2復(fù)合電極的析氫催化性能的調(diào)控。

    Abstract:

    Ni-6W alloy strip with 70μm thick was used as substrate, nanoporous NiW was prepared by anodic oxidation method, and then CeO2 was deposited by chemical decomposition method on nanoporous NiW to prepare NiW-nano-CeO2 electrode. The morphology structure of the NiW, nanoporous NiW and NiW-nano-CeO2 three electrodes were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and XPS. The electrochemical hydrogen evolution behaviors of the three electrodes were characterized by cathodic polarization curves, cyclic voltammetry curves and electrochemical impedance techniques. The results show that NiW-nano-CeO2 electrode has the highest electrocatalytic hydrogen evolution performance, which is mainly due to the three-dimensional nanoporous structure, small mass transfer impedance, large electrochemically active specific surface area and the synergistic effect between NiW and CeO2. When used as an electrocatalyst for hydrogen evolution, the current density reaches 100 mA cm-2 in 1M NaOH solution, it is 55 mV and 81 mV lower than that of NiW-CeO2 lectrode and NiW electrode, respectively. The impedance spectra obtained were fitted and analyzed, and the influence of CeO2 on the electrochemical process of the whole hydrogen evolution process was analyzed. The results show that the hydrogen evolution performance of the (200) crystal-exposed nano-porous NiW-CeO2 electrode is better than that of the Ni (111) crystal-exposed NiW-CeO2 electrode and the non-preferential orientation Ni-S/ CeO2, Ni-Zn/ CeO2 electrode. The composite electrode has a higher exchange current density of 1.7 × 10-1A cm-2 than the co-deposited Ni-CeO2 reported in the literature. In this paper, the morphology of CeO2 was controlled by this method, and then the (200) crystal face was selectively exposed to control the catalytic performance of NiW-CeO2 composite electrode for hydrogen evolution.

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李亞寧,李廣忠,楊保軍.氧化鈰-鎳鎢復(fù)合電極的制備及其析氫催化性能[J].稀有金屬材料與工程,2023,52(3):1022~1026.[Li Yaning, Li Guangzhong, Yang Baojun. Preparation of cerium oxide Ni-W composite electrode and its Catalytic performance for hydrogen evolution reaction[J]. Rare Metal Materials and Engineering,2023,52(3):1022~1026.]
DOI:10.12442/j. issn.1002-185X.20220736

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  • 收稿日期:2022-09-15
  • 最后修改日期:2022-11-04
  • 錄用日期:2022-11-24
  • 在線發(fā)布日期: 2023-04-07
  • 出版日期: 2023-03-24