Industrial Research Institute of Nonwovens & Technical Textiles, Shandong Center for Engineered Nonwovens, College of Textiles & Clothing, Qingdao University, Qingdao 266071 Shandong, P. R. China.
School of Materials Science and Engineering, Shandong University of Science and Technology, Qingdao 266071 Shandong, P. R. China.
Inorg Chem. 2023 Feb 13;62(6):2826-2837. doi: 10.1021/acs.inorgchem.2c04154. Epub 2023 Jan 29.
Constructing three-dimensional (3D) hierarchical heterostructures is an appealing but challenging strategy to improve the performance of catalysts for electrical energy devices. Here, an efficient and robust flexible self-supporting catalyst, interface coupling of ultrathin CoFe-LDH nanosheets and CoO nanowire arrays on the carbon cloth (CC/CoO@CoFe-LDH), was proposed for boosting oxygen evolution reaction (OER) in rechargeable liquid/solid Zn-air batteries (ZABs). The strong interfacial interaction between the CoFe-LDH and CoO heterostructures stimulated the charge redistribution in their coupling regions, which improved the electron conductivity and optimized the adsorption free energy of OER intermediates, ultimately boosting the intrinsic OER performance. Besides, the 3D hierarchical nanoarray structure facilitated the exposure of catalytically active centers and rapid electron/mass transfer during the OER process. As such, the CC/CoO@CoFe-LDH catalyst achieved excellent OER catalytic activity in alkaline medium, with a small overpotential of 237 mV at 10 mA cm, a low Tafel slope of 35.43 mV dec, and long-term durability of up to 48 h, significantly outperforming the commercial RuO catalyst. More impressively, the liquid and flexible solid-state ZABs assembled by the CC/CoO@CoFe-LDH hybrid catalyst as the OER catalyst presented a stable open circuit voltage, large power density, superb cycling life, and satisfactory flexibility, indicating great potential applications in energy technology. This work provides a good guidance for the development of advanced electrocatalysts with heterostructures and an in-depth understanding of electronic modulation at the heterogeneous interface.
构建三维(3D)分层异质结构是提高电能源器件催化剂性能的一种很有吸引力但具有挑战性的策略。在这里,提出了一种高效且稳健的柔性自支撑催化剂,即超薄 CoFe-LDH 纳米片和 CoO 纳米线阵列在碳布(CC/CoO@CoFe-LDH)上的界面耦合,用于提升可再充电液/固锌空气电池(ZAB)中的析氧反应(OER)。CoFe-LDH 和 CoO 异质结构之间的强界面相互作用刺激了它们耦合区域内的电荷重新分布,提高了电子导电性并优化了 OER 中间体的吸附自由能,最终提升了内在的 OER 性能。此外,3D 分层纳米阵列结构有利于在 OER 过程中暴露催化活性中心和促进快速电子/质量转移。因此,CC/CoO@CoFe-LDH 催化剂在碱性介质中表现出优异的 OER 催化活性,在 10 mA cm 时具有 237 mV 的小过电势、35.43 mV dec 的低塔菲尔斜率和长达 48 h 的长期耐久性,明显优于商业 RuO 催化剂。更令人印象深刻的是,由 CC/CoO@CoFe-LDH 混合催化剂作为 OER 催化剂组装的液体和柔性固态 ZAB 呈现出稳定的开路电压、高功率密度、卓越的循环寿命和令人满意的柔韧性,表明其在能源技术中有很大的应用潜力。这项工作为具有异质结构的先进电催化剂的发展提供了良好的指导,并深入了解了异质界面处的电子调制。