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1.
析氢催化电极的研究现状   总被引:14,自引:1,他引:13  
综述了析氢反应中高催化活性电极的现状,并对析氢催化机理进行了评述。  相似文献   

2.
电沉积Ni-W-P合金上析氢行为的研究   总被引:5,自引:1,他引:4  
在1mol/L的KOH水溶液中,以电沉积法制备的Ni-Co-P、Ni-W-P合金为阴极,测量析氢时的极化曲线,结果表明,与Ni电极相比,Ni-W-P合金电极上氢析出的电势正移200次毫伏,即Ni-W-P合金电极具有较高的析氢电催化活性。通过SEM和XPS分析探讨了Ni电极中引入W和P元素对析氢催化活性的影响。  相似文献   

3.
高催化活性析氢电极的制备现状   总被引:1,自引:0,他引:1  
对高催化活性析氢电极的各种制备方法(如电沉积法、去合金法、化学镀、复合镀、溅射法及机械合金化等)进行了归纳,并指出了今后析氢电极的发展趋势.  相似文献   

4.
硅电极表面镍钨磷合金电沉积及其析氢性能   总被引:1,自引:0,他引:1  
李爱昌  李健飞  任宁  刘爽 《材料保护》2004,37(11):5-6,41
Ni-W-P合金薄膜具有优良的催化析氢性能和耐蚀性.通过在半导体p型Si上恒电流沉积Ni-W-P合金薄膜,制备出Ni-W-P合金修饰的半导体p型Si电极.用SEM和XRD对合金薄膜的表面形貌、组成和结构进行了表征,以电极的阴极极化曲线对其催化析氢和光电催化析氢性能进行评价.结果表明:W,P质量分数分别为26.71%和0.95%的纳米晶合金修饰的p型Si电极具有优良的催化析氢性能和显著的光电析氢活性.  相似文献   

5.
杨余芳  罗娟 《材料保护》2020,(8):79-84+95
以海绵镍为基体,采用单脉冲电沉积与复合镀相结合的方法制备了多孔Ni-WC复合电极材料;运用扫描电镜(SEM)和X射线衍射仪(XRD)表征镀层的表面形貌和相结构,并研究了WC浓度和脉冲参数对多孔Ni-WC复合电极在0.5 mol/L H2SO4溶液中的电催化析氢性能的影响。结果表明:Ni-WC复合材料的表面晶粒细小、致密,呈多孔结构。随着镀液中WC浓度、脉冲电流密度和占空比的增大,多孔Ni-WC复合电极的析氢阴极极化减小,交换电流密度增大,电化学交流阻抗减小,Ni-WC多孔电极的析氢活性增强。循环伏安曲线和计时电流曲线表明,多孔Ni-WC复合电极具有较好的抗腐蚀性和析氢稳定性。  相似文献   

6.
脉冲电沉积制备Ni-W-Fe-La纳米晶析氢电极材料   总被引:1,自引:0,他引:1  
脉冲电沉积合金层较为复杂,目前尚未实际应用。采用脉冲电沉积技术制备了Ni-W-Fe-La纳米晶合金析氢镀层,利用扫描电镜、X射线衍射仪、能谱仪等设备测试了合金镀层的形貌、结构和组成。研究了制备工艺对镀层析氢性能的影响。确定了合金镀层的最佳制备工艺条件:机械搅拌下,控制平均电流密度Jm=5A/dm2,峰值电流密度Jp=14A/dm2,占空比R为35%,脉冲频率f=150Hz,pH值6.0~6.5,脉冲时间30min,镀液温度35℃。结果表明:制备的Ni-W-Fe-La镀层为纳米级镀层,其晶粒尺寸为48.73nm;稀土La元素的加入能够明显改变镀层表面形貌、晶粒尺寸以及镀层的耐蚀和析氢电催化活性,析氢电位比直流电沉积所得的同类镀层明显正移。  相似文献   

7.
以泡沫镍为基体电沉积制备了Ni-S涂层电极.通过对电流密度、电沉积温度、电沉积时间和镀液pH值等条件对涂层析氢性能影响的研究,确定了适宜的电沉积工艺条件;电极涂层的XRD、SEM测试结果表明涂层为非晶态结构、表面颗粒大小均匀且具较大表面积;电解过程中出现了Ni3S2由非晶态向晶态的转变,由于Ni3S2具有较强的吸附氢能力,是析氢反应的催化活性中心,电解过程中Ni3S2的出现降低了电极的析氢电位.模拟电解水实验结果表明泡沫镍基Ni-S涂层电极较Raney-Ni电极具有更好的析氢活性.  相似文献   

8.
非晶态Fe-Mo合金在碱性溶液中的电催化析氢活性   总被引:4,自引:1,他引:3  
研究了电沉积制备的非晶态Fe-Mo合金(组成分别为Fe82Mo18、Fe74Mo26和Fe71Mo29)电极在30%KOH溶液中,303~343K的温度范围内的析氢催化性能。三种非晶态合金都显示出较好的催化析氢活性。温度为343K,析H2电流密度为300nA/cm^2时的析H2过电位为150~157mV。非晶态Fe82Mol8、Fe74Mo26和Fe71Mo29合金上析H2反应的表观活化能分别为57.18,47.33,102.28kJ/mol。  相似文献   

9.
赵静  陈必清  景欣欣  翟佳鑫 《功能材料》2022,(6):6085-6094+6111
采用恒电位电沉积技术,在氯化胆碱-尿素体系中制备Ni-Fe-Sm/Cu稀土合金电极并研究其析氢(HER)性能。通过阴极极化曲线(LSV)、循环伏安曲线(CV)等电化学测试方法及SEM等表征技术,研究沉积条件对稀土合金电极的析氢性能及其表面形貌的影响。结果表明,添加稀土元素Sm能够有效提升合金电极的析氢性能。在-1.22 V的沉积电位下,沉积20 min制备的Ni-Fe-Sm/Cu稀土合金电极析氢性能最佳。在10 mA/cm2电流密度下,稀土合金电极的析氢过电位仅115 mV,Tafel斜率最小,析氢反应受Volmer-Heyrovsky反应控制。且该条件下制备的Ni-Fe-Sm/Cu稀土合金具备最高的双电层电容,电催化活性表面积最大。通过交流阻抗法(EIS)可知,Ni-Fe-Sm/Cu合金电极具有较高电荷转移速率。此外,Ni-Fe-Sm/Cu稀土合金电极在碱性介质中具有较好的稳定性,在经过1000圈的循环侧安测试,电催化析氢性能没有明显变化。  相似文献   

10.
泡沫镍基镍硫合金涂层形貌、结构和析氢性能研究   总被引:4,自引:0,他引:4  
在含有柠檬酸、硫脲和少许糖精的Watt镀液中,用电沉积的方法在镍泡沫基体上制备了镍硫合金涂层.各层涂层的形貌用SEM分析,各层硫量的分布用EDX测量.第1层涂层的结构用XRD测定.对各种电极包括镍泡沫基、镍网基上镍硫涂层电极,空白镍泡沫、镍网电极等的极氢电位进行了测量,研究了不同温度下镍泡沫基镍硫涂层电极的析氢活性.结果表明,镍泡沫基Ni-S涂层电极的析氢活性比镍网基Ni-S涂层电极活性高得多.镍泡沫各层硫量呈梯度的分布规律,由表及里硫含量逐步降低,中心层硫含量最低.各层表面微细颗粒大小及其均一性不相同,第1层的颗粒尺寸大于其它层的颗粒,其大小均一性也较其它层差.镍硫涂层是镍和Ni3S2组成的非晶态,使涂层具有丰富的表面积和氢气析出反应的活性中心.在加热的电解液中,在60℃以下和60℃以上的温区内电极析氢反应的机制不完全一样,受温度影响的程度也不一样.4000A/m2、90℃时,这种电极的析氢电位比15℃时析氢电位低180mV.  相似文献   

11.
高析氢催化活性和稳定性的纳米晶Ni-Fe-Mo-Co合金   总被引:3,自引:0,他引:3  
在酸性柠檬酸盐-氯化物体系中电沉积得到铁族金属与钼多元合金,通过SEM、XRD和EDS对合金的表面形貌、微观结构和组成进行分析,结果表明Ni-Fe-Mo-Co电极为纳米晶,晶粒尺寸为3.7nm;电解后电极表面呈现"蜂窝"型网孔结构,平均孔径约50nm,具有很大的真实表面积和机械稳定性.通过比较不同的铁族金属与钼合金电极在30%KOH溶液中的催化性能,表明在Ni-Fe-Mo三元合金中引入Co能进一步提高合金的催化活性.纳米晶Ni-Fe-Mo-Co合金电极在80℃和200mA/cm2时,过电位为66.2mV,与其它铁族金属与钼合金电极相比较,其显示出更高的催化活性.长期和间断电解实验,说明纳米晶Ni-Fe-Mo-Co合金电极具有良好的催化稳定性能.  相似文献   

12.
We present a straightforward method for one-pot electrodeposition of platinum atoms-doped molybdenum oxide (Pt·MoO3−x) films and show their superior electrocatalytic activity in the hydrogen evolution reaction (HER). A ~15-nm-thick Pt·MoO3−x film was prepared by one-pot electrodeposition at −0.8 V for 1 ms. Due to considerably different solute concentrations, the content of Pt atoms in the electrodeposited composite electrocatalyst is low. No Pt crystals or islands were observed on the flat Pt·MoO3−x films, indicating that Pt atoms were homogeneously dispersed within the MoO3−x thin film. The catalytic performance and physicochemical features of Pt·MoO3−x as a HER electrocatalyst were characterized. The results showed that our Pt·MoO3−x film exhibits 23- and 11-times higher current density than Pt and MoO3−x electrodeposited individually under the same conditions, respectively. It was found that the dramatic enhancement in the HER performance was principally due to the abundant oxygen defects. The use of the developed one-pot electrodeposition and doping method can potentially be extended to various catalytically active metal oxides or hydroxides for enhanced performance in various energy storage and conversion applications.  相似文献   

13.
High gravimetric energy density, earth-abundance, and environmental friendliness of hydrogen sources have inspired the utilization of hydrogen fuel as a clean alternative to fossil fuels. Hydrogen evolution reaction (HER), a half reaction of water splitting, is crucial to the low-cost production of pure H2 fuels but necessitates the use of electrocatalysts to expedite reaction kinetics. Owing to the availability of low-cost oxygen evolution reaction (OER) catalysts for the counter electrode in alkaline media and the lack of low-cost OER catalysts in acidic media, researchers have focused on developing HER catalysts in alkaline media with high activity and stability. Nickel is well-known as an HER catalyst and continuous efforts have been undertaken to improve Ni-based catalysts as alkaline electrolyzers. In this review, we summarize earlier studies of HER activity and mechanism on Ni surfaces, along with recent progress in the optimization of the Ni-based catalysts using various modern techniques. Recently developed Ni-based HER catalysts are categorized according to their chemical nature, and the advantages as well as limitations of each category are discussed. Among all Ni-based catalysts, Ni-based alloys and Ni-based hetero-structure exhibit the most promising electrocatalytic activity and stability owing to the fine-tuning of their surface adsorption properties via a synergistic nearby element or domain. Finally, selected applications of the developed Ni-based HER catalysts are highlighted, such as water splitting, the chloralkali process, and microbial electrolysis cell.
  相似文献   

14.
镍-铁-磷/金刚石复合沉积工艺与性能研究   总被引:2,自引:2,他引:2  
以三元合金为基体的复合电沉积层综合了一般耐磨镀层的性能和所镶嵌的固体微粒的性能.为开发新型多元非晶态合金耐磨复合沉积层,以复合沉积层耐磨减摩性为主要衡量指标并综合考虑其他性能指标,用正交试验法进行了镍-铁-磷/金刚石复合电沉积工艺与性能的研究.结果表明,在试验所采用的复合电沉积工艺控制范围内,可获得金刚石微粒弥散分布的镍-铁-磷/金刚石复合电沉积层,通过调整沉积工艺参数,能得到不同金刚石微粒复合量的复合电沉积层;在镀态下该复合沉积层(基质)呈非晶态结构;较佳综合性能复合层的电沉积工艺参数为:镀液中金刚石微粒(0.5~1.0 μm)含量6 g/L;NaH2PO2·H2O含量2 g/L;FeSO4·7H2O含量70 g/L,其对制备具有良好摩擦学特性的镍-铁-磷/金刚石复合沉积层具有重要的参考价值.  相似文献   

15.
Hydrogen evolution reaction (HER) through water splitting is a promising way to solve the energy short-age.Noble-metal-free HER electrocatalysts with high efficiency is very important for practical applica-tions.Herein,we prepare the Ni3S4@MoS2 electrocatalyst on carbon cloth (CC) through a two-step hy-drothermal process.The Ni3S4 nanorods are uniformly integrated with the MoS2 nanosheets,forming a hierarchical structure and heterogeneous interfaces.The fast electron transfer on the interface en-hances the kinetics of catalytic reaction.The hierarchical structure provides more exposed active sites.The Ni3S4@MoS2/CC exhibits good catalytic activity and long-term stability for HER.This work provided a practicable strategy to develop efficient electrocatalysts for HER in alkaline media.  相似文献   

16.
Tailoring of nickel-sulfur (Ni-S) intermetallic compound film electrodes for hydrogen evolution reaction in alkaline solutions was attempted by electrodeposition from a typical Watts bath containing sodium thiosulfate as sulfur source and sulfosalicylic acid as additive. The XRD analysis shows that the as-deposited Ni-S film electrode with fine morphological features comprised of intermetallic compound phase structure and amorphous phase structure. The intermetallic compound film electrodes generate a higher catalytic activity for the hydrogen evolution reaction in alkaline solution in comparison with Ni-S film electrodes comprised of amorphous phase structures, even with commercial Ni mesh or Ni/RuO2 composite electrode.  相似文献   

17.
18.
高效非贵金属催化剂对于推进析氢反应(HER)的大规模工业化至关重要.碳化钼(Mo2C)因其类似铂的能带密度和优良的中间产物吸附特性,有望替代贵金属基材料成为具有前景的催化剂.然而,它在常规制备过程中存在严重的晶体过度生长和团聚问题,导致催化效率低.本研究利用三聚氰胺辅助法制备了含有丰富表面和界面的超细碳化钼/氮化钼(Mo2C/Mo2N)异质结构,并同时将其嵌入到氮掺杂碳纳米纤维(CNFs)中.Mo2C/Mo2N异质结构的协同作用与超细纳米晶表面暴露的丰富活性位点共同提高了电催化活性,而氮掺杂碳纳米纤维框架保证了快速的电荷转移和良好的结构稳定性.此外,原位形成的Mo2C/Mo2N晶体与碳基质之间存在较强的界面耦合作用,进一步提高了电子电导率和电催化活性.得益于这些优势,Mo2C/Mo2N@N-CNFs在碱性溶液中表现出优异的电催化析氢性能,在电流密度10 mV cm-2时具有75 mV的低过电势,优于单相Mo2C@N-CNFs对比样以及近期报道的Mo2C/Mo2N基催化剂.这个合成方法集成了异质结构、纳米化和碳修饰策略,为设计高效率电催化材料提供了新的参考.  相似文献   

19.
用于析氢反应(HER)的低成本、高效能催化剂对于推进基于清洁氢气的能源工业非常重要.二维二硫化钼(MoS2)具有显著的催化性能,因而已被人们广泛深入研究.然而,大多数现有的合成方法耗时、复杂且效率较低.本文通过超快(60秒)微波引发的方法生产MoS2/石墨烯催化剂.石墨烯的高比表面积和导电性为MoS2纳米片的生长提供了有利的导电网络和快速电荷转移动力.文中制备的MoS2/石墨烯纳米复合材料在酸性介质中对HER表现出优异的电催化活性,具有62 mV的低起始电位,高阴极电流和43.3mV/dec的Tafel斜率.除了优异的催化活性外, MoS2/石墨烯还具有较长的循环稳定性,在250 mV的过电位下阴极电流密度高达1000 mA cm^-2.此外, MoS2/石墨烯催化剂在30–120°C范围内具有出色的HER活性和36.51 kJ mol^-1的低活化能,提供了潜在的大批量生产和制备的机会.  相似文献   

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