Lu Yi, Fan Deqi, Chen Zupeng, Xiao Weiping, Cao Cancan, Yang Xiaofei
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, College of Science, Nanjing Forestry University, Nanjing 210037, China.
Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zürich, CH-8093 Zürich, Switzerland.
Sci Bull (Beijing). 2020 Mar 30;65(6):460-466. doi: 10.1016/j.scib.2019.12.020. Epub 2019 Dec 28.
Rational design and controllable synthesis of efficient electrocatalysts for water oxidation is of significant importance for the development of promising energy conversion systems, in particular integrated photoelectrochemical water splitting devices. Cobalt oxide (CoO) nanostructures with mixed valences (II,III) have been regarded as promising electrocatalysts for the oxygen evolution reaction (OER). They are able to promote catalytic support of OER but with only modest activity. Here, we demonstrate that the OER performance of cubic CoO electrocatalyst is obviously improved when they are anchored on delaminated two-dimensional (2D) TiC MXene nanosheets. Upon activation the overpotential of the hybrid catalyst delivers 300 mV at a current density of 10 mA cm in basic solutions, which is remarkably lower than those of TiC MXene and CoO nanocubes. The strong interfacial electrostatic interactions between two components contribute to the exceptional catalytic performance and stability. The enhanced OER activity and facile synthesis make these CoO nanocubes-decorated ultrathin 2D TiC MXene nanosheets useful for constructing efficient and stable electrodes for high-performance electrochemical water splitting.
合理设计并可控合成用于水氧化的高效电催化剂对于开发有前景的能量转换系统,特别是集成光电化学水分解装置具有重要意义。具有混合价态(II,III)的氧化钴(CoO)纳米结构被认为是用于析氧反应(OER)的有前景的电催化剂。它们能够促进OER的催化支持,但活性仅适中。在此,我们证明当立方CoO电催化剂锚定在分层的二维(2D)TiC MXene纳米片上时,其OER性能明显提高。在碱性溶液中,混合催化剂在电流密度为10 mA cm时的过电位为300 mV,这明显低于TiC MXene和CoO纳米立方体的过电位。两种组分之间强烈的界面静电相互作用有助于其优异的催化性能和稳定性。增强的OER活性和简便的合成方法使得这些CoO纳米立方体修饰的超薄2D TiC MXene纳米片可用于构建用于高性能电化学水分解的高效稳定电极。