Enhanced electrocatalytic performance for oxygen evolution reaction via active interfaces of Co3O4arrays@FeOx/Carbon cloth heterostructure by plasma-enhanced atomic layer deposition.
Qingying ZhuGuoyong YangLimin TangHongwei MiLingna SunQianling ZhangLibo DengPeixin ZhangXiangzhong RenYongliang LiPublished in: Nanotechnology (2023)
Oxygen evolution reaction (OER) is a necessary procedure in various devices including water splitting and rechargeable metal-air batteries but required a higher potential to improve oxygen evolution efficiency due to its slow reaction kinetics. In order to solve this problem, a heterostructured electrocatalyst (Co3O4@FeOx/CC) is synthesized by deposition of iron oxides (FeOx) on carbon cloth (CC) via plasma-enhanced atomic layer deposition (PE-ALD), then growth of the cobalt oxide (Co3O4) nanosheet arrays. The deposition cycle of FeOx on the CC strongly influences the in-situ growth and distribution of Co3O4 nanosheets and electronic conductivity of the electrocatalyst. Owing to the high accessible and electroactive areas and improved electrical conductivity, the free-standing electrode of Co3O4@FeOx/CC with 100 deposition cycles of FeOx exhibits excellent electrocatalytic performance for OER with a low overpotential of 314.0 mV at 10 mA cm-2 and a small Tafel slope of 29.2 mV dec-1 in alkaline solution, which is much better than that of Co3O4/CC (448 mV), and even commercial RuO2 (380 mV). This design and optimization strategy shows a promising way to synthesize ideally designed catalytic architectures for application in energy storage and conversion.