Fei Wu, Biao Wu, Liang Chen, Yunan Wang, Jiejie Li and Qiuju Zhang
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引用次数: 0
Abstract
Asymmetric nickel oxyhydroxide (NiOOH) possesses multi-OH and O active sites on different surfaces, (001) and (00), which possibly causes a complicated catalytic process. Density functional theory (DFT) calculations reveal that the unconventional dual-site mechanism (UDSM) of the oxygen evolution reaction (OER) on NiOOH (001) and (00) exhibits significantly lower overpotentials of 0.80 and 0.77 V, compared to 1.24 and 1.62 V for the single-site mechanism (SSM), respectively. Through chemical doping or heterojunction modifications, the constructed NiOOH@FeOOH (00) heterojunction reduces the thermodynamic overpotential to 0.49 V from original 0.77 V undergoing the UDSM. Although Fe/Co-doping or physical compression yield similar or slightly higher overpotentials and are not conductive to facilitating the OER process by the UDSM, all dual-site paths exhibit obviously lower overpotentials than the SSM for pristine and regulated NiOOH (001) and (00) from the whole viewpoint. This work identifies a more reasonable and efficient dual-site OER mechanism, which is expected to help the rational design of highly-efficient electrocatalysts.
期刊介绍:
Nanoscale is a high-impact international journal, publishing high-quality research across nanoscience and nanotechnology. Nanoscale publishes a full mix of research articles on experimental and theoretical work, including reviews, communications, and full papers.Highly interdisciplinary, this journal appeals to scientists, researchers and professionals interested in nanoscience and nanotechnology, quantum materials and quantum technology, including the areas of physics, chemistry, biology, medicine, materials, energy/environment, information technology, detection science, healthcare and drug discovery, and electronics.