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锚定在掺杂介孔网络碳骨架上的原子级分散镍/硫化镍:提升在碱性和酸性介质中的氧还原反应性能。

Atomically dispersed Ni/NiS anchored on doped mesoporous networked carbon framework: Boosting the ORR performance in alkaline and acidic media.

作者信息

Tyagi Alekha, Kar Kamal K, Yokoi Hiroyuki

机构信息

Advanced Nanoengineering Materials Laboratory, Materials Science Programme, Indian Institute of Technology, Kanpur, Uttar Pradesh 208016, India.

Advanced Nanoengineering Materials Laboratory, Materials Science Programme, Indian Institute of Technology, Kanpur, Uttar Pradesh 208016, India; Advanced Nanoengineering Materials Laboratory, Department of Mechanical Engineering, Indian Institute of Technology, Kanpur, Uttar Pradesh 208016, India.

出版信息

J Colloid Interface Sci. 2020 Jul 1;571:285-296. doi: 10.1016/j.jcis.2020.03.043. Epub 2020 Mar 20.

DOI:10.1016/j.jcis.2020.03.043
PMID:32203765
Abstract

Rational and strategic fabrication of cost-effective, active and durable oxygen reduction reaction (ORR) electrocatalyst is the bottle-neck for the commercialization of fuel cells and metal-air batteries. Atomically dispersed nickel (Ni)/nickel sulfide (NiS) anchored on heteroatom doped networked hierarchical porous carbonaceous sheets are synthesized from nickel nitrate and guanidine thiocyanate. The sample annealed at 750 °C followed by acid-treatment (Ni-GT-750-A) emerges as the best performing pH-universal ORR catalyst with an onset potential of 0.91 (0.1 M KOH) and 0.89 V (0.1 M HClO) vs. reversible hydrogen electrode (RHE). It also exhibits better current durability (95.0 and 60%) and methanol tolerance (90.6 and 80.3%) in comparison to the commercial catalyst (65.0, 27, -33.0 and 16.5%) in alkaline and acidic media, respectively. An insight into the microstructure and ORR-active chemical sites is obtained with the aid of electron microscopic (FE-SEM and HR-TEM) and physiochemical (sorption isotherm, XRD, Raman and XPS) studies, respectively. The enhanced activity results from the synergistic influence of metallic ORR-active sites in hierarchical porous doped defective carbon support, which provides the well-interlinked conducting channel for electron transfer and additional ORR-active sites. The introduced electrocatalyst establishes Ni decorated doped carbon systems as potential revolutionary substitutes for commercial systems.

摘要

合理且策略性地制备具有成本效益、活性高且耐用的氧还原反应(ORR)电催化剂是燃料电池和金属空气电池商业化的瓶颈。通过硝酸镍和硫氰酸胍合成了锚定在杂原子掺杂的网络化分级多孔碳质薄片上的原子分散镍(Ni)/硫化镍(NiS)。在750℃退火后进行酸处理的样品(Ni-GT-750-A)成为性能最佳的pH通用ORR催化剂,相对于可逆氢电极(RHE),其起始电位在0.1M KOH中为0.91V,在0.1M HClO中为0.89V。与商业催化剂相比,它在碱性和酸性介质中分别还表现出更好的电流耐久性(95.0%和60%)和甲醇耐受性(90.6%和80.3%)(商业催化剂在碱性和酸性介质中的相应数据分别为65.0%、27%、-33.0%和16.5%)。分别借助电子显微镜(FE-SEM和HR-TEM)和物理化学(吸附等温线、XRD、拉曼和XPS)研究,深入了解了微观结构和ORR活性化学位点。活性增强源于分级多孔掺杂缺陷碳载体中金属ORR活性位点的协同影响,该载体为电子转移提供了相互连通良好的导电通道以及额外的ORR活性位点。所引入的电催化剂使镍修饰的掺杂碳体系成为商业体系潜在的革命性替代品。

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