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膜电极厚度对电极材料析氢活性的影响
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作者 宋红 李伟 +2 位作者 张德坤 张庆宝 耿新华 《人工晶体学报》 EI CAS CSCD 北大核心 2007年第1期62-65,共4页
用直流磁控溅射法制备不同厚度的膜电极材料。在室温,1mol/L KOH溶液中,这些膜电极材料析氢反应的过电位和膜电极的厚度有关:在一定厚度范围内,膜电极越厚,析氢过电位越小,不同膜电极材料都表现出这样的规律,只是大小和对厚度的依赖程... 用直流磁控溅射法制备不同厚度的膜电极材料。在室温,1mol/L KOH溶液中,这些膜电极材料析氢反应的过电位和膜电极的厚度有关:在一定厚度范围内,膜电极越厚,析氢过电位越小,不同膜电极材料都表现出这样的规律,只是大小和对厚度的依赖程度有所不同。这些结果表明析氢反应不只是发生在电极表面的范围内,反应过程中形成的金属氢化物由于深入到材料内部,从而出现了厚度对析氢反应过电位的影响,并且由于材料不同,可形成的金属氢化物厚度不同,所以对过电位的影响也就不同。 展开更多
关键词 析氢电极材料 厚度 过电位
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溅射腔气压对电极材料析氢活性的影响
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作者 宋红 张庆宝 +1 位作者 魏长春 耿新华 《人工晶体学报》 EI CAS CSCD 北大核心 2006年第6期1291-1295,共5页
采用直流磁控溅射法制备了析氢反应的电极材料-N iFe,CoMo,研究了在1.0Pa^4.0Pa的范围内,不同溅射腔气压条件下制备的电极材料的晶粒尺寸、析氢反应的过电位与气压的关系,结果显示过电位随气压升高而降低,而且在2.0Pa处,过电位变化的程... 采用直流磁控溅射法制备了析氢反应的电极材料-N iFe,CoMo,研究了在1.0Pa^4.0Pa的范围内,不同溅射腔气压条件下制备的电极材料的晶粒尺寸、析氢反应的过电位与气压的关系,结果显示过电位随气压升高而降低,而且在2.0Pa处,过电位变化的程度和Tafel斜率均发生突变,表明不同溅射气压下制备的材料晶粒尺寸的变化,引起了析氢反应控制步骤的改变。 展开更多
关键词 析氢电极材料 气压 过电位 晶粒尺寸
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新型电极材料的研究进展
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作者 汪永霞 王敏敏 《分析化学进展》 2021年第3期200-216,共17页
电解水是大规模制氢的重要途径,为了降低阳极阴极过电位以节约能耗,研究开发低过电位、高催化活性的电极材料具有重要的意义。影响电极材料催化活性的主要因素有结构因素和能量因素。本文主要简述了电解水的基本原理,以及电极材料的研... 电解水是大规模制氢的重要途径,为了降低阳极阴极过电位以节约能耗,研究开发低过电位、高催化活性的电极材料具有重要的意义。影响电极材料催化活性的主要因素有结构因素和能量因素。本文主要简述了电解水的基本原理,以及电极材料的研究现状,期待未来能够开发出具有低过电位、高催化活性和高稳定性的新型电解水电极材料。 展开更多
关键词 电解水 电极材料 析氢电极材料 结构 催化活性
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Preparation and electrochemical characterization of activated carbons by chemical-physical activation 被引量:4
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作者 张治安 崔沐 +2 位作者 赖延清 李劼 刘业翔 《Journal of Central South University》 SCIE EI CAS 2009年第1期91-95,共5页
A process was proposed based on the combination of chemical and physical activation for the production of activated carbons used as the electrode material for electric double layer capacitor (EDLC). By material charac... A process was proposed based on the combination of chemical and physical activation for the production of activated carbons used as the electrode material for electric double layer capacitor (EDLC). By material characterization and electrochemical methods, the influences of the activitation process on the specific surface area, pore structure and electrochemical properties of the activated carbons were investigated. The results show that specific surface area, the mesopore volume, and the specific capacitance increase with the increase of the mass ratio of KOH to char (m(KOH)/m(char)) and the activation time, respectively. When m(KOH)/m(char) is 4.0, the specific surface area and the mesopore volume reach the maximum values, i.e. 1 960 m2/g and 0.308 4 cm3/g, and the specific capacitance is 120.7 F/g synchronously. Compared with the chemical activation, the activated carbons prepared by chemical-physical activation show a larger mesopore volume, a higher ratio of mesopore and a larger specific capacitance. 展开更多
关键词 activated carbon electric double layer capacitor chemical-physical activation pore structure
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Research progresses of cathodic hydrogen evolution in advanced lead–acid batteries 被引量:9
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作者 Feng Wang Chen Hu +5 位作者 Min Zhou Kangli Wang Jiali Lian Jie Yan Shijie Cheng Kai Jiang 《Science Bulletin》 SCIE EI CAS CSCD 2016年第6期451-458,共8页
Integrating high content carbon into the negative electrodes of advanced lead–acid batteries effectively eliminates the sulfation and improves the cycle life,but brings the problem of hydrogen evolution,which increas... Integrating high content carbon into the negative electrodes of advanced lead–acid batteries effectively eliminates the sulfation and improves the cycle life,but brings the problem of hydrogen evolution,which increases inner pressure and accelerates the water loss.In this review,the mechanism of hydrogen evolution reaction in advanced lead–acid batteries,including lead–carbon battery and ultrabattery,is briefly reviewed.The strategies on suppression hydrogen evolution via structure modifications of carbon materials and adding hydrogen evolution inhibitors are summarized as well.The review points out effective ways to inhibit hydrogen evolution and prolong the cycling life of advanced lead–acid battery,especially in high-rate partial-state-of-charge applications. 展开更多
关键词 Lead–carbon battery ULTRABATTERY Hydrogen evolution reaction Hydrogen inhibition
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Facile synthesis and excellent electrochemical performance of CoP nanowire on carbon cloth as bifunctional electrode for hydrogen evolution reaction and supercapacitor 被引量:3
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作者 宋杰芳 向建勇 +5 位作者 牟从普 王博翀 温福昇 苏灿 王聪 柳忠元 《Science China Materials》 SCIE EI CSCD 2017年第12期1179-1186,共8页
In this paper, we report CoP nanowires supported on carbon cloth (CC) (CoP/CC) as a bifunctional electrode for hydrogen evolution reaction (HER) and supercapacitor. CoP/CC possess an excellent electrocatalytic p... In this paper, we report CoP nanowires supported on carbon cloth (CC) (CoP/CC) as a bifunctional electrode for hydrogen evolution reaction (HER) and supercapacitor. CoP/CC possess an excellent electrocatalytic performance for HER, with a Tafel slope of 56 mV/dec and a low overpotential of 68 mV to achieve a current density of 10 mAcm^-2. Remarkably, the bifunctional CoP/CC used as electrode for supercapacitor exhibit a higher specific capacitance of 674 F g^-1 at a scan rate of 5 mV s^-1 and maintains long-life cycling stability, retaining 86% of the initial capacitance after 10,000 cycles. CoP/CC will be a promising candidate as electrode for HER and supercapacitor. 展开更多
关键词 cobalt phosphide nanowire hydrogen evolution reaction SUPERCAPACITOR
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