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电催化甲酸氧化反应过程中AgPd纳米合金颗粒的表面重构

Surface reconstruction of AgPd nanoalloy particles during the electrocatalytic formate oxidation reaction.

作者信息

Guo Longfei, Chen Fuyi, Jin Tao, Liu Huazhen, Zhang Nan, Jin Yachao, Wang Qiao, Tang Quan, Pan Bowei

机构信息

State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, Xi'an 710072, China.

School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an, 710072, China.

出版信息

Nanoscale. 2020 Feb 7;12(5):3469-3481. doi: 10.1039/c9nr09660d. Epub 2020 Jan 28.

Abstract

Formate is a kind of carbon-neutral fuel that can be synthesized by electrochemical conversion of CO, however, the generated aqueous formate electrolyte is still short of potential application. Here, formate solution is proposed to be utilized as anode fuels of direct formate fuel cells through the formate oxidation reaction (FOR), and graphene supported AgPd nanoalloys (AgPd/rGO) are prepared to catalyze the FOR. Specifically, the mass activity of the as-prepared AgPd/rGO catalyst is 4.21 A mg and the retention activity of AgPd/rGO is 49.1% of initial activity after successive 500 cycles, which is 2.48 and 3.03 times higher than that of unsupported AgPd nanoalloys. When increasing the positive scan limit from 0.0 to 0.8 V, the mass activity of the AgPd/rGO catalyst increases from 2.32 to 6.03 A mg and Pd surface coverage increases from 51.87% to 62.42%, indicating the occurrence of surface reconstruction where Pd atoms migrate to the surface of AgPd nanoalloys, and less intensive reconstruction is observed in unsupported AgPd nanoalloys, whose mass activity increases from 1.35 to 2.49 A mg. The driving force and kinetic path are calculated for the surface reconstruction induced by the adsorption of H, O and C atoms, in the case of C atoms on graphene, the segregation energy of surface Pd atoms in the AgPd nanoalloy is -1.16 eV, and the activation energy for the migration of subsurface Pd atoms to the surface is 0.54 eV, which are lower than the segregation (0.03 eV) and activation (2.06 eV) energy on a clean alloy surface.

摘要

甲酸盐是一种可通过CO的电化学转化合成的碳中性燃料,然而,所生成的甲酸盐水性电解质仍缺乏潜在应用。在此,提出通过甲酸盐氧化反应(FOR)将甲酸盐溶液用作直接甲酸盐燃料电池的阳极燃料,并制备了石墨烯负载的AgPd纳米合金(AgPd/rGO)来催化FOR。具体而言,所制备的AgPd/rGO催化剂的质量活性为4.21 A mg,在连续500次循环后,AgPd/rGO的保留活性为初始活性的49.1%,分别是无负载AgPd纳米合金的2.48倍和3.03倍。当将正扫描极限从0.0 V增加到0.8 V时,AgPd/rGO催化剂的质量活性从2.32 A mg增加到6.03 A mg,Pd表面覆盖率从51.87%增加到62.42%,这表明发生了表面重构,其中Pd原子迁移到AgPd纳米合金表面,而在无负载AgPd纳米合金中观察到的重构强度较小,其质量活性从1.35 A mg增加到2.49 A mg。计算了由H、O和C原子吸附引起的表面重构的驱动力和动力学路径,在石墨烯上的C原子的情况下,AgPd纳米合金中表面Pd原子的偏析能为-1.16 eV,亚表面Pd原子迁移到表面的活化能为0.54 eV,低于清洁合金表面上的偏析能(0.03 eV)和活化能(2.06 eV)。

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