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Non-Precious Cathode Electrocatalytic Materials for Zinc-Air Battery

机译:锌空气电池的非贵金属阴极电催化材料

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摘要

In the past decade, rechargeable batteries attracted the attention from the researchers in search for renewable and sustainable energy sources. Up to date, lithium-ion battery is the most commercialized and has been supplying power to electronic devices and hybrid and electric vehicles. Lithium-ion battery, however, does not satisfy the expectations of ever-increasing energy and power density, which of their limits owes to its intercalation chemistry and the safety.1-2 Therefore, metal-air battery drew much attention as an alternative for its high energy density and a simple cell configuration.1 There are several different types of metal-air batteries that convey different viable reaction mechanisms depending on the anode metals; such as Li, Al, Ca, Cd, and Zn. Redox reactions take place in a metal-air cell regardless of the anode metal; oxidation reaction at the anode and reduction reaction at the air electrode. Between the two reaction, the oxygen reduction reaction (ORR) at the air electrode is the relatively the limiting factor within the overall cell reactions. The sluggish ORR kinetics greatly affects the performance of the battery system in terms of power output, efficiency, and durability. Therefore, researchers have put tremendous efforts in developing highly efficient metal air batteries and fuel cells, especially for high capacity applications such as electric vehicles. Currently, the catalyst with platinum nanoparticles supported on carbon material (Pt-C) is considered to exhibit the best ORR activities. Despite of the admirable electrocatalytic performance, Pt-C suffers from its lack of practicality in commercialization due to their prohibitively high cost and scarcity as of being a precious metal. Thus, there is increasing demand for replacing Pt with more abundant metals due economic feasibility and sustainability of this noble metal.3-5 Two different attitudes are taken for solution. The first approach is by optimizing the platinum loading in the formulation, or the alternatively the platinum can be replaced with non-precious materials. The purpose of this work is to discover and synthesize alternative catalysts for metal-air battery applications through optimized method without addition of precious metals.Different non-precious metals are investigated as the replacement of the precious metal including transition metal alloys, transition metal or mixed metal oxides, and chalcogenides. These types of metals, alone, still exhibits unsatisfying, yet worse, kinetics in comparison to the precious metals. Nitrogen-doped carbon material is a recently well studied carbon based material that exhibits great potential towards the cathodic reaction.6 Nitrogen-doped carbon materials are found to exhibit higher catalytic activity compared to the mentioned types of metals for its improved conductivity. Benefits of the carbon based materials are in its abundance and minimal environmental footprints. However, the degradation of these materials has demonstrated loss of catalytic activity through destruction of active sites containing the transition metal centre, ultimately causing infeasible stability. To compensate for these drawbacks and other limits of the nitrogen-doped carbon based catalysts, nitrogen-doped carbon nanotubes (NCNT) are also investigated in the series of study. The first investigation focuses on a development of a simple method to thermally synthesize a non-precious metal based nitrogen-doped graphene (NG) electrocatalyst using exfoliated graphene (Ex-G) and urea with varying amounts of iron (Fe) precursor. The morphology and structural features of the synthesized electrocatalyst (Fe-NG) were characterized by SEM and TEM, revealing the existence of graphitic nanoshells that potentially contribute to the ORR activity by providing a higher degree of edge plane exposure. The surface elemental composition of the catalyst was analyzed through XPS, which showed high content of a total N species (~8 at.%) indicative of the effective N-doping, present mostly in the form of pyridinic nitrogen groups. The oxygen reduction reaction (ORR) performance of the catalyst was evaluated by rotating disk electrode voltammetry in alkaline electrolyte and in a zinc-air battery cell. Fe-NG demonstrated high onset and half-wave potentials of -0.023 V (vs. SCE) and -0.110 V (vs. SCE), respectively. This excellent ORR activity is translated into practical zinc-air battery performance capabilities approaching that of commercial platinum based catalyst.Another approach was made in the carbon materials to further improve the cost of the electrode. Popular carbon allotropes, CNT and graphene, are combined as a composite (GC) and heteroatoms, nitrogen and sulfur, are introduced in order to improve the charge distribution of the graphitic network. Dopants were doped through two step processes; nitrogen dopant was introduced into the graphitic framework followed by the sulfur dopant. The coexistence of the two heteroatoms as dopants demonstrated outstanding ORR performance to those of reported as metal free catalysts. Furthermore, effects of temperature were investigated through comparing ORR performances of the catalysts synthesized in two different temperatures (500 ℃ and 900 ℃) during the N-doping process (consistent temperature was used for S-doping). Through XPS analysis of the surface chemistry of catalysts produced with high temperature during the N-doping step showed absence of N-species after the subsequent S-doping process (GC-NHS). Thus, the synergetic effects of the two heteroatoms were not revealed during the half-cell testing. Meanwhile, the two heteroatoms were verified in the catalyst synthesized though using low temperature during the N-doping process followed by the S-doping step (GC-NLS). Consequently, ORR activity of the resulting material demonstrated promising onset and half-wave potentials of -0.117 V (vs. SCE) and -0.193 V (vs. SCE).In combination of these investigations, this document introduces thorough study of novel materials and their performance in its application as ORR catalyst in metal air batteries. Moreover, this report provides detailed fundamental insights of carbon allotropes, and their properties as potential elecrocatalysts and essential concepts in electrochemistry that lies behind zinc-air batteries. The outstanding performances of carbon based electrocatalyst are reviewed and used as the guides for further direction in the development of metal-air batteries as a promising sustainable energy resource in the future.
机译:在过去的十年中,可充电电池吸引了研究人员的注意力,以寻找可再生和可持续的能源。迄今为止,锂离子电池是最商业化的,并一直为电子设备以及混合动力和电动汽车供电。然而,锂离子电池不能满足不断增长的能量和功率密度的期望,其极限是由于其插层化学性质和安全性。1-2因此,金属空气电池作为锂离子电池的替代品备受关注。它有很高的能量密度和简单的电池配置。1有几种不同类型的金属空气电池,它们根据阳极金属传递不同的可行反应机理。例如Li,Al,Ca,Cd和Zn。氧化还原反应在金属空气电池中发生,与阳极金属无关。阳极发生氧化反应,空气电极发生还原反应。在这两个反应之间,空气电极处的氧还原反应(ORR)是整个电池反应中的相对限制因素。缓慢的ORR动力学会在功率输出,效率和耐用性方面极大地影响电池系统的性能。因此,研究人员在开发高效的金属空气电池和燃料电池方面付出了巨大的努力,特别是在电动汽车等大容量应用中。当前,具有负载在碳材料(Pt-C)上的铂纳米颗粒的催化剂被认为表现出最佳的ORR活性。尽管Pt-C具有令人赞叹的电催化性能,但由于其价格过高和作为稀有金属的稀缺性,使其在商业化方面缺乏实用性。因此,由于这种贵金属的经济可行性和可持续性,用更丰富的金属代替Pt的需求不断增加。3-5解决方案采取两种不同的态度。第一种方法是通过优化配方中的铂含量,或者可以用非贵重材料代替铂。这项工作的目的是通过优化方法发现和合成用于金属-空气电池的替代催化剂,而无需添加贵金属。研究了各种非贵金属作为贵金属的替代品,包括过渡金属合金,过渡金属或混合金属。金属氧化物和硫族化物。与贵金属相比,仅这些类型的金属仍表现出不令人满意的动力学,但更糟糕的是动力学。氮掺杂碳材料是一种经过充分研究的碳基材料,具有很大的阴极反应潜力。6与上述类型的金属相比,氮掺杂碳材料由于具有更高的电导率,因此具有更高的催化活性。碳基材料的好处在于它的丰富性和最小的环境足迹。然而,这些材料的降解已显示出通过破坏包含过渡金属中心的活性位点而丧失了催化活性,最终导致了不可行的稳定性。为了弥补这些缺点和氮掺杂碳基催化剂的其他局限性,在一系列研究中还研究了氮掺杂碳纳米管(NCNT)。首次研究的重点是开发一种简单的方法,该方法使用片状石墨烯(Ex-G)和尿素与不同量的铁(Fe)前驱体热合成非贵金属基氮掺杂石墨烯(NG)电催化剂。 SEM和TEM对合成的电催化剂(Fe-NG)的形貌和结构特征进行了表征,揭示了石墨纳米壳的存在,通过提供更高程度的边缘平面暴露,它们可能对ORR活性有贡献。通过XPS分析了催化剂的表面元素组成,表明存在高含量的总N种类(〜8 at。%),表明有效的N掺杂,主要以吡啶氮基团形式存在。通过旋转盘电极伏安法在碱性电解质和锌-空气电池单元中评估催化剂的氧还原反应(ORR)性能。 Fe-NG的高起跳电位和半波电位分别为-0.023 V(vs. SCE)和-0.110 V(vs. SCE)。这种出色的ORR活性转化为实用的锌-空气电池性能,接近商用铂基催化剂。在碳材料中采用了另一种方法,以进一步提高电极成本。常见的碳同素异形体CNT和石墨烯被组合为复合物(GC)和杂原子,氮和硫为了改善石墨网络的电荷分布,引入了。掺杂剂通过两个步骤进行掺杂。将氮掺杂剂引入石墨骨架中,然后引入硫掺杂剂。这两种杂原子作为掺杂剂的共存表现出与报道的无金属催化剂相比出色的ORR性能。此外,通过比较两种不同温度(500℃和900℃)在N掺杂过程中合成的催化剂的ORR性能(使用恒定温度进行S掺杂),研究了温度的影响。通过XPS分析,在N掺杂步骤中高温生产的催化剂的表面化学性质表明,在随后的S掺杂过程(GC-NHS)之后,没有N物种。因此,在半电池测试期间未显示两个杂原子的协同作用。同时,在N掺杂过程中使用低温,然后进行S掺杂步骤(GC-NLS),在合成的催化剂中验证了这两个杂原子。因此,所得材料的ORR活性显示出令人满意的-0.117 V(vs. SCE)和-0.193 V(vs. SCE)的起伏和半波电势。结合这些研究,本文件介绍了对新型材料和它们在金属空气电池中用作ORR催化剂的性能。此外,本报告提供了碳同素异形体的详细基础见解,以及它们作为潜在的触媒催化剂的性质以及锌空气电池背后的电化学基本概念。综述了碳基电催化剂的出色性能,并将其用作指导,以指导金属-空气电池作为未来有希望的可持续能源的发展方向。

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    Kim Baejung;

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  • 年度 2013
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  • 正文语种 en
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