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负载于氮掺杂碳上的缺陷型Fe O 少原子簇作为高性能锌空气电池的高效氧还原电催化剂

Defective Fe O Few-Atom Clusters Anchored on Nitrogen-Doped Carbon as Efficient Oxygen Reduction Electrocatalysts for High-Performance Zinc-Air Batteries.

作者信息

Chu Panpan, Zhang Yingmeng, He Jiajie, Chen Jinhong, Zhuang Jingjun, Li Yongliang, Ren Xiangzhong, Zhang Peixin, Sun Lingna, Yu Bingzhe, Chen Shaowei

机构信息

College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong, 518060, P. R. China.

Department of Chemistry and Biochemistry, University of California, Santa Cruz, CA, 95064, USA.

出版信息

Small Methods. 2022 Jul;6(7):e2200207. doi: 10.1002/smtd.202200207. Epub 2022 Jun 3.

DOI:10.1002/smtd.202200207
PMID:35656764
Abstract

It remains a challenge to develop cost-effective, high-performance oxygen electrocatalysts for rechargeable metal-air batteries. Herein, zinc-mediated zeolitic imidazolate frameworks are exploited as the template and nitrogen and carbon sources, onto which is deposited a Fe O layer by plasma-enhanced atomic layer deposition. Controlled pyrolysis at 1000 °C leads to the formation of high density of Fe O few-atom clusters with abundant oxygen vacancies deposited on an N-doped graphitic carbon framework. The resulting nanocomposite (Fe O /NC-1000) exhibits a markedly enhanced electrocatalytic performance toward oxygen reduction reaction in alkaline media, with a remarkable half-wave potential of +0.930 V versus reversible hydrogen electrode, long-term stability, and strong tolerance against methanol poisoning, in comparison to samples prepared at other temperatures and even commercial Pt/C. Notably, with Fe O /NC-1000 as the cathode catalyst, a zinc-air battery delivers a high power density of 158 mW cm and excellent durability at 5 mA cm with stable 2000 charge-discharge cycles over 600 h. This is ascribed to the ready accessibility of the Fe O catalytic active sites, and enhanced electrical conductivity, oxygen adsorption, and electron-transfer kinetics by surface oxygen vacancies. Further contributions may arise from the highly conductive and stable N-doped graphitic carbon frameworks.

摘要

开发用于可充电金属空气电池的具有成本效益的高性能氧电催化剂仍然是一项挑战。在此,锌介导的沸石咪唑酯骨架被用作模板以及氮和碳源,通过等离子体增强原子层沉积在其上沉积一层FeO层。在1000℃下进行受控热解导致形成高密度的FeO少数原子簇,其具有大量氧空位,沉积在氮掺杂的石墨碳骨架上。所得的纳米复合材料(FeO/NC-1000)在碱性介质中对氧还原反应表现出显著增强的电催化性能,相对于可逆氢电极具有+0.930 V的显著半波电位、长期稳定性以及对甲醇中毒的强耐受性,与在其他温度下制备的样品甚至商业Pt/C相比。值得注意的是,以FeO/NC-1000作为阴极催化剂,锌空气电池在5 mA cm下提供158 mW cm的高功率密度和优异的耐久性,在600小时内具有稳定的2000次充放电循环。这归因于FeO催化活性位点易于接近,以及表面氧空位增强了电导率、氧吸附和电子转移动力学。高度导电且稳定的氮掺杂石墨碳骨架可能会有进一步贡献。

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