Jia Zhe, Zhao Yilu, Wang Qing, Lyu Fucong, Tian Xiaobao, Liang Shun-Xing, Zhang Lai-Chang, Luan Junhua, Wang Qianqian, Sun Ligang, Yang Tao, Shen Baolong
School of Materials Science and Engineering, Jiangsu Key Laboratory for Advanced Metallic Materials, Southeast University, Nanjing 211189, China.
School of Materials Science and Engineering, Harbin Institute of Technology, Shenzhen 518055, China.
ACS Appl Mater Interfaces. 2022 Mar 2;14(8):10288-10297. doi: 10.1021/acsami.1c22294. Epub 2022 Feb 17.
Scaling up the production of cost-effective electrocatalysts for efficient water splitting at the industrial level is critically important to achieve carbon neutrality in our society. While noble-metal-based materials represent a high-performance benchmark with superb activities for hydrogen and oxygen evolution reactions, their high cost, poor scalability, and scarcity are major impediments to achieve widespread commercialization. Herein, a flexible freestanding Fe-based metallic glass (MG) with an atomic composition of FeNiPC was prepared by a large-scale metallurgical technique that can be employed directly as a bifunctional electrode for water splitting. The surface hydroxylation process created unique structural and chemical heterogeneities in the presence of amorphous FeOOH and NiP as well as nanocrystalline NiP that offered various active sites to optimize each rate-determining step for water oxidation. The achieved overpotentials for the oxygen evolution reaction were 327 and 382 mV at high current densities of 100 and 500 mA cm in alkaline media, respectively, and a cell voltage of 1.59 V was obtained when using the MG as both the anode and the cathode for overall water splitting at a current density of 10 mA cm. Theoretical calculations unveiled that amorphous FeOOH makes a significant contribution to water molecule adsorption and oxygen evolution processes, while the amorphous and nanocrystalline NiP stabilize the free energy of hydrogen protons (Δ) in the hydrogen evolution process. This MG alloy design concept is expected to stimulate the discovery of many more high-performance catalytic materials that can be produced at an industrial scale with customized properties in the near future.
扩大具有成本效益的电催化剂的生产规模,以在工业水平上实现高效的水分解,对于实现我们社会的碳中和至关重要。虽然基于贵金属的材料代表了用于析氢和析氧反应的具有卓越活性的高性能基准,但它们的高成本、差的可扩展性和稀缺性是实现广泛商业化的主要障碍。在此,通过大规模冶金技术制备了一种原子组成为FeNiPC的柔性独立式铁基金属玻璃(MG),其可直接用作水分解的双功能电极。表面羟基化过程在非晶态FeOOH和NiP以及纳米晶NiP存在的情况下产生了独特的结构和化学不均匀性,这些提供了各种活性位点来优化水氧化的每个速率决定步骤。在碱性介质中,析氧反应在100和500 mA cm²的高电流密度下实现的过电位分别为327和382 mV,当使用MG作为阳极和阴极进行全水分解且电流密度为10 mA cm²时,获得了1.59 V的电池电压。理论计算表明,非晶态FeOOH对水分子吸附和析氧过程有重大贡献,而非晶态和纳米晶NiP在析氢过程中稳定了氢质子的自由能(Δ)。这种MG合金设计概念有望在不久的将来刺激发现更多可在工业规模生产且具有定制性能的高性能催化材料。