Department of Chemistry and Biochemistry, Texas State University 601 University Drive, San Marcos, Texas 78666, United States.
Department of Physics and Astronomy, University of Texas at San Antonio One UTSA Circle, San Antonio, Texas 78249, United States.
ACS Appl Mater Interfaces. 2017 Jun 7;9(22):18660-18674. doi: 10.1021/acsami.7b00043. Epub 2017 May 30.
Electrochemical oxygen reduction reaction (ORR) catalysts that have both high activities and long-term stabilities are needed for proton-exchange membrane fuel cells (PEMFCs) and metal-air batteries. Two-dimensional (2D) materials based on graphene have shown high catalytic activities, however, carbon-based materials result in significant catalyst degradation due to carbon oxidation that occurs at high electrochemical potentials. Here, we introduce the synthesis and electrochemical performance of metallic 2D nanoframes which represent a new approach to translate 2D materials into unsupported (carbon-free) electrocatalysts that have both significantly higher ORR catalytic activities and stabilities compared with conventional Pt/carbon electrocatalysts. Metallic Ni-Pt 2D nanoframes were synthesized by controlled thermal treatments of Pt-decorated Ni(OH) nanosheets. The nanoframes consist of a hierarchical 2D framework composed of a highly catalytically active Pt-Ni alloy phase with an interconnected solid and pore network that results in three-dimensional molecular accessibility. The inclusion of Ni within the Pt structure resulted in significantly smaller Pt lattice distances compared to those of Pt nanoparticles. On the basis of its unique local and extended structure, the ORR specific activity of Ni-Pt 2D nanoframes (5.8 mA cm) was an order of magnitude higher than Pt/carbon. In addition, accelerated stability testing at elevated potentials up to 1.3 V showed that the metallic Ni-Pt nanoframes exhibit significantly improved stability compared with Pt/carbon catalysts. The nanoarchitecture and local structure of metallic 2D nanoframes results in high combined specific activity and elevated potential stability. Analysis of the ORR electrochemical reaction kinetics on the Ni-Pt nanoframes supports that at low overpotentials the first electron transfer is the rate-determining step, and the reaction proceeds via a four electron reduction process. The ability to create metallic 2D structures with 3D molecular accessibility opens up new opportunities for the design of high activity and stability carbon-free catalyst nanoarchitectures for numerous electrocatalytic and catalytic applications.
用于质子交换膜燃料电池(PEMFC)和金属-空气电池的电化学氧气还原反应(ORR)催化剂需要同时具有高活性和长期稳定性。基于石墨烯的二维(2D)材料表现出高催化活性,然而,由于在高电化学势下发生的碳氧化,碳基材料导致催化剂严重降解。在这里,我们介绍了金属 2D 纳米框架的合成和电化学性能,这代表了一种将 2D 材料转化为无载体(无碳)电催化剂的新方法,与传统的 Pt/C 电催化剂相比,这种电催化剂具有更高的 ORR 催化活性和稳定性。通过对 Pt 修饰的 Ni(OH)纳米片进行控制的热处理合成了金属 Ni-Pt 2D 纳米框架。纳米框架由高度催化活性的 Pt-Ni 合金相组成的分层 2D 框架组成,具有相互连接的固体和孔网络,从而导致三维分子可及性。Pt 结构中包含 Ni 导致 Pt 晶格距离明显小于 Pt 纳米颗粒。基于其独特的局部和扩展结构,Ni-Pt 2D 纳米框架的 ORR 比 Pt/C 高一个数量级。此外,在高达 1.3 V 的升高电位下进行的加速稳定性测试表明,与 Pt/C 催化剂相比,金属 Ni-Pt 纳米框架表现出显著提高的稳定性。金属 2D 纳米框架的纳米结构和局部结构导致高的比活性和升高电位稳定性。对 Ni-Pt 纳米框架上的 ORR 电化学反应动力学的分析表明,在低过电势下,第一个电子转移是速率决定步骤,反应通过四电子还原过程进行。创建具有 3D 分子可及性的金属 2D 结构的能力为设计用于众多电催化和催化应用的高活性和稳定性无碳催化剂纳米结构开辟了新的机会。