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Carbon-based Bifunctional Electrocatalysts for Metal-air Battery Applications

机译:金属-空气电池应用的碳基双功能电催化剂

摘要

The ever-increasing energy consumption and the environmental issues from the excessive rely on fossil fuels have triggered intensive research on the next generation power sources. Metal-air batteries, as one of the most promising technologies emerged, have attracted enormous attention due to its low cost, environmental benignity and high energy density. Among all types of metal-air batteries, Zn-air batteries in particular have tremendous potential for use as alternative energy storage primarily by the low-cost, abundance, low equilibrium potential, environmental benignity, a flat discharge voltage and a longer shell life. However, there are still issues in pertinent to the anode, electrolyte and cathode that remain to be overcome. In particular, the electrocatalyst at the cathode of a metal-air battery which catalyzes the electrochemistry reactions during charge and discharge of the cell plays the most crucial role for the successful commercialization of the metal-air technology.A series of studies from the carbon nanofibres to spinel cobalt oxide and perovskite lanthanum nickelate was conducted to explore the ORR/OER catalytic properties of those materials which lead to further investigations of the non-precious metal oxide/carbon hybrids as bifunctional catalysts. Introducing ORR active species such as nitrogen, sulfur, boron and phosphorus into high surface area carbon has been an effective strategy to fabricate high catalytic activity ORR electrocatalyst. Carbon nanofibre is an abundant, low cost and conductive material that has tremendous potential as ORR catalyst, especially via KOH activation and nitrogen-doping post-treatments. These two post-treatment methods serve as simplistic methodologies to enhance the carbon surface area and ORR catalytic activity of the pristine carbon nanofibres, respectively. The activated and nitrogen-doped carbon nanofibres demonstrated 26% of improved half-wave potential and 17% of increased limiting current density as a comparison to the pristine carbon nanofibre via RDE testing in alkaline electrolyte. To realize the catalytic activity of activated and nitrogen-doped carbon nanofibres in a more practical condition, they are further evaluated in Zn-air batteries. Polarization curves retrieved from Zn-air cell testing showed 75% higher voltage obtained by activated and nitrogen-doped carbon nanofibres than pristine carbon nanofibres at 70mAcm-2 current density. Structured oxides such as spinels and perovskites have been widely reported as ORR and OER catalyst in metal-air batteries. It is widely known that the properties of nanostructures are closely pertinent to their morphologies. The initial performance and durability of cubic Co3O4 synthesized from Feng et al and LaNiO3 from modified sol-gel method are tested in RDE system. After the durability testing, the ORR onset potential and limiting current density of cubic Co3O4 has decreased by 50% and 25%, respectively, whereas the OER limiting current density dropped significantly from ~15mAcm2 to almost zero current density. LaNiO3 with different particle sizes synthesized from modified sol-gel method was prepared and evaluated in RDE system. A particle size related performance can be clearly seen from the RDE results. The ORR limiting current of the lanthanum nickelate with smaller particle size (LNO-1) is higher than that of lanthanum nickelate with larger particle size (LNO-0) by 40% and the OER limiting current of LNO-1 is almost tripled that of LNO-0.With the previous experience on carbon material and structured oxides, two hybrid bifunctional catalysts were prepared and their performance was evaluated. cCo3O4/ExNG was made by physically mixing of cCo3O4 with ExNG with 1to 1 ratio. The hybrid showed enhanced bifunctional catalytic activities compared to each of its individual performance. Based on the voltammetry results, a significant positive shift (+0.16V) in ORR half-wave potential and tripled limiting current were observed in the case of the hybrid compared to the pure cobalt oxide. By combing cCo3O4 and ExNG, the OER limiting current of the hybrid exceeds that of cCo3O4 by ca. 33% and four-fold that of the ExNG. The kinetic current density at -0.4V for cCo3O4/ExNG is 15.9 mAcm-2 which is roughly 4 times the kinetic current density of the ExNG (3.8 mAcm-2) and over 10 times greater than that of cCo3O4 (1.1 mAcm-2). Electrochemical impedance spectroscopy showed that the charge transfer resistance of the hybrid is ca. one third of cCo3O4 and roughly only one half of ExNG which suggests a more efficient electrocatalysis of the hybrid on the air electrode than the other two.Mixing structured oxides with carbon material provides a simple method of fabricating bifunctional catalysts, however the interactions between those two materials are quite limited. In-situ synthesis of cCo3O4/MWCNT hybrid by chemically attaching cCo3O4to the acid-functionalized MWCNT is able to provide strong interactions between its components. Through RDE testing, the ORR activity of cCo3O4/MWCNT outperformed its individual component showing the highest onset potential (-0.15V) and current density (-2.91 mAcm-2 at -0.4V) with ~4 electron transfer pathway. Moreover, the MWCNT and cCo3O4 suffered from significant OER degradation after cycling (92% and 94%, respectively) whereas the hybrid material demonstrated an outstanding stability with only 15% of performance decrease, which is also far more superior to the physical mixture (30% higher current density).Among all the catalyst studied, cCo3O4/MWCNT has the highest performance and durability. The excellent performance of the hybrid warrants further in-depth research of non-precious metal oxide/carbon hybrids and the information presented in this thesis will create afoundation for future investigation towards high performance and durability bifunctional electrocatalysts for metal-air battery applications.
机译:过度依赖化石燃料的不断增长的能源消耗和环境问题引发了对下一代电源的深入研究。作为最有前途的技术之一,金属空气电池由于其低成本,环境友好和高能量密度而备受关注。在所有类型的金属空气电池中,尤其是锌空气电池具有巨大的潜力,主要是因为其成本低,容量丰富,平衡电位低,环境友好,放电电压平坦以及使用寿命更长等优点,可以用作替代能源存储。然而,与阳极,电解质和阴极有关的问题仍然有待克服。特别地,在金属-空气电池的阴极处的电催化剂在电池的充电和放电期间催化电化学反应,对于金属-空气技术的成功商业化起着至关重要的作用。从碳纳米纤维到尖晶石型氧化钴和钙钛矿型镍酸镧进行了一系列研究,以探索这些材料的ORR / OER催化性能,从而进一步研究了作为双功能催化剂的非贵金属氧化物/碳杂化物。在高表面积碳中引入氮,硫,硼和磷等ORR活性物质已成为制备高催化活性ORR电催化剂的有效策略。碳纳米纤维是一种丰富,低成本且导电的材料,具有作为ORR催化剂的巨大潜力,特别是通过KOH活化和氮掺杂后处理。这两种后处理方法用作简化方法,分别用于提高原始碳纳米纤维的碳表面积和ORR催化活性。与通过碱性电解质中RDE测试得到的原始碳纳米纤维相比,活性碳和掺杂氮的碳纳米纤维表现出26%的半波电势提高和17%的极限电流密度提高。为了在更实际的条件下实现活性碳和氮掺杂碳纳米纤维的催化活性,需要在锌空气电池中对其进行进一步评估。从锌空气电池测试获得的极化曲线显示,在70mAcm-2的电流密度下,活性碳和氮掺杂的碳纳米纤维所获得的电压比原始碳纳米纤维高75%。尖晶石和钙钛矿等结构氧化物已被广泛报道为金属-空气电池中的ORR和OER催化剂。众所周知,纳米结构的性质与其形态密切相关。在RDE系统中测试了Feng等人合成的立方晶Co3O4和改良的溶胶-凝胶法合成的LaNiO3的初始性能和耐久性。经过耐久性测试后,立方晶Co3O4的ORR起始电势和极限电流密度分别降低了50%和25%,而OER极限电流密度从〜15mAcm2显着下降到几乎为零的电流密度。采用改进的溶胶凝胶法合成了不同粒径的LaNiO3,并在RDE系统中进行了评价。从RDE结果可以清楚地看到与粒度有关的性能。粒径较小的镍酸镧(LNO-1)的ORR极限电流比粒径较大的镍酸镧(LNO-0)的ORR极限电流高40%,LNO-1的OER极限电流几乎是粒径的三倍。 LNO-0。根据碳材料和结构氧化物的先前经验,制备了两种杂化双功能催化剂,并对其性能进行了评估。 cCo3O4 / ExNG通过将cCo3O4与ExNG以1:1的比例进行物理混合而制得。与杂种的每种性能相比,杂种显示出增强的双功能催化活性。根据伏安法的结果,与纯氧化钴相比,在混合动力系统中,观察到ORR半波电势有明显的正移(+ 0.16V),极限电流增加了三倍。通过组合cCo3O4和ExNG,混合动力汽车的OER极限电流超过cCo3O4的极限电流。是ExNG的33%和四倍。 cCo3O4 / ExNG在-0.4V时的动电流密度为15.9 mAcm-2,大约是ExNG(3.8 mAcm-2)的动电流密度的4倍,比cCo3O4(1.1 mAcm-2)的动电流密度大10倍以上。 。电化学阻抗谱显示杂化体的电荷转移电阻为。三分之一的cCo3O4和大约只有一半的ExNG,这表明杂化剂在空气电极上的电催化比其他两种更有效。结构化氧化物与碳材料的混合提供了一种制备双功能催化剂的简单方法,但是这两种材料之间的相互作用非常有限。通过将cCo3O4化学连接到酸官能化的MWCNT上,原位合成cCo3O4 / MWCNT杂化物能够在其组分之间提供强大的相互作用。通过RDE测试,cCo3O4 / MWCNT的ORR活性优于其单独的组分,显示出最高的起始电势(-0.15V)和电流密度(-0.4V时为-2.91 mAcm-2),具有约4个电子传输路径。此外,MWCNT和cCo3O4在循环后会发生显着的OER降解(分别为92%和94%),而杂化材料表现出出色的稳定性,仅降低15%的性能,这也远远优于物理混合物(30在所有研究的催化剂中,cCo3O4 / MWCNT具有最高的性能和耐用性。杂化物的优异性能保证了对非贵金属氧化物/碳杂化物的进一步深入研究,并且本文中所提供的信息将为今后针对金属-空气电池应用的高性能和耐用性双功能电催化剂的研究奠定基础。

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    Liu Yulong;

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  • 年度 2013
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  • 原文格式 PDF
  • 正文语种 en
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