Abad Jose M, Martínez-Huerta María Victoria, Cebollada Jesús, Sainz Raquel, Pita Marcos, De Lacey Antonio L
Instituto de Catálisis y Petroleoquímica, CSIC. C/Marie Curie 2, Madrid 28049, Spain.
ACS Omega. 2025 May 7;10(19):19552-19563. doi: 10.1021/acsomega.5c00165. eCollection 2025 May 20.
The oxygen evolution reaction (OER) is the main bottleneck in water splitting and other key technologies due to its slow kinetics. The development of low-cost, highly active, stable, and more efficient electrocatalysts as an alternative to the commonly expensive and scarce Ir- and Ru-based catalysts used is necessary. The present work reports the preparation of OER catalysts by a straightforward and easy method based on the synergistic effect of Ni/Ferrocene combination that leads to high current densities, lower overpotential, high stability, and low Tafel slope in alkaline conditions. The optimized Ni/Ferrocene catalyst demonstrates exceptional performance, providing a constant potential of ∼1.51 and ∼1.65 V and overpotentials of ∼0.278 and ∼0.420 V for more than 26 and 46 h at current densities of 10 and 100 mA·cm, respectively. It represents an important and significant advance in obtaining electrocatalyst materials for OER anodes without the need for previous and tedious synthetic procedures. Only commercial chemicals with low amounts of metals are employed, thus facilitating that this Ni/ferrocene configuration could be scaled up to real devices.
析氧反应(OER)因其缓慢的动力学过程,成为水分解及其他关键技术的主要瓶颈。开发低成本、高活性、稳定且更高效的电催化剂作为常用的昂贵且稀缺的铱基和钌基催化剂的替代品很有必要。目前的工作报道了一种基于镍/二茂铁组合的协同效应,通过直接且简便的方法制备OER催化剂,该方法在碱性条件下可实现高电流密度、低过电位、高稳定性和低塔菲尔斜率。优化后的镍/二茂铁催化剂表现出卓越性能,在电流密度分别为10和100 mA·cm时,可分别在超过26小时和46小时的时间内提供约1.51 V和约1.65 V的恒定电位以及约0.278 V和约0.420 V的过电位。这代表了在无需先前繁琐合成程序的情况下获得用于OER阳极的电催化剂材料方面取得的重要且显著的进展。仅使用了低金属含量的商业化学品,因此便于将这种镍/二茂铁结构扩大到实际装置中。