Highly acid-durable carbon coated Co3O4 nanoarrays as efficient oxygen evolution electrocatalysts

析氧 材料科学 化学工程 电催化剂 氧还原 氧还原反应 氧气 碳纤维 电化学 纳米技术 化学 复合数 有机化学 电极 复合材料 工程类 物理化学
作者
Xiulin Yang,Henan Li,Ang‐Yu Lu,Shixiong Min,Zacharie Idriss,Mohamed Nejib Hedhili,Kuo‐Wei Huang,Hicham Idriss,Lain‐Jong Li
出处
期刊:Nano Energy [Elsevier BV]
卷期号:25: 42-50 被引量:254
标识
DOI:10.1016/j.nanoen.2016.04.035
摘要

Most oxygen evolution reaction (OER) electrocatalysts are not stable in corrosive acids. Even the expensive RuO2 or IrO2, the most acid-resistant oxides, can be dissolved at an oxidative potential. Herein, we realize that the failures of OER catalysts are mostly caused by the weak interface between catalysts and the substrates. Hence, the study of the interface structure between catalysts and substrates is critical. In this work, we observe that the cheap OER catalysts Co3O4 can be more durable than the state-of-the-art RuO2 if the interface quality is good enough. The Co3O4 nanosheets deposited on carbon paper (Co3O4/CP) is prepared by electroplating of Co-species and followed by a two-step calcination process. The 1st step occurs in vacuum in order to maintain the surface integrity of the carbon paper and converts Co-species to Co(II)O. The 2nd step is a calcination in ambient conditions which enables the complete transformation of Co(II)O to Co3O4 without degrading the mechanical strength of the Co3O4-CP interface. Equally important, an in situ formation of a layer of amorphous carbon on top of Co3O4 further enhances the OER catalyst stability. Therefore, these key advances make the Co3O4 catalyst highly active toward the OER in 0.5 M H2SO4 with a small overpotential (370 mV), to reach 10 mA/cm2. The observed long lifetime for 86.8 h at a constant current density of 100 mA/cm2, is among the best of the reported in literature so far, even longer than the state-of-art RuO2 on CP. Overall, our study provides a new insight and methodology for the construction of a high-performance and high stability OER electrocatalysts in corrosive acidic environments.
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