Liu Zhiwei, Wang Zhaowu, Lv Diandian, Yang Hongyuan, Kang Zhenhui, Ghosh Suptish, Menezes Prashanth W, Chen Ziliang
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, 199 Ren'ai Road, Suzhou, Jiangsu, 215123, China.
School of Science, Hebei University of Technology, Tianjin, 300401, China.
Adv Mater. 2025 Feb;37(7):e2311997. doi: 10.1002/adma.202311997. Epub 2025 Jan 2.
The electrochemical two-electron oxygen reduction reaction (2e ORR) offers a sustainable pathway for the production of HO; however, the development of electrocatalysts with exceptional activity, selectivity, and long-term stability remains a challenging task. Herein, a novel approach is presented to addressing this challenge by synthesizing hierarchical hollow SmPO nanospheres with open channels via a two-step hydrothermal treatment. The produced compound demonstrates remarkable 2e selectivity, exceeding 93% across a wide potential range of 0.0-0.6 V in 0.1 m KOH, with a peak of 96% at 0.45 V. When employed as the cathode in a flow cell, the synthesized SmPO exhibits impressive stability at 100 mA cm for 12 h, consistently achieving a Faradaic efficiency above 90%. Using X-ray absorption, in situ Raman and Fourier-transform infrared spectroscopies, theoretical calculations, and post-ORR assessments, it is found that this hollow compound possesses intrinsic open channels and is characterized by the optimal metal atomic spacing, and exceptional structural and compositional stabilities. These factors significantly enhance the thermodynamics, kinetics, and stability of the 2e ORR process. Notably, the produced compound also exhibits outstanding 2e ORR performance in neutral environments. Furthermore, this strategy can be extended to other hollow rare-earth-P-O compounds, demonstrating excellent 2e ORR performance under both neutral and alkaline conditions.
电化学双电子氧还原反应(2e ORR)为过氧化氢的生产提供了一条可持续的途径;然而,开发具有卓越活性、选择性和长期稳定性的电催化剂仍然是一项具有挑战性的任务。在此,我们提出了一种新颖的方法来应对这一挑战,即通过两步水热法合成具有开放通道的分级中空磷酸钐纳米球。所制备的化合物表现出显著的2e选择性,在0.1 m KOH中0.0 - 0.6 V的宽电位范围内超过93%,在0.45 V时达到峰值96%。当用作流动电池的阴极时,合成的磷酸钐在100 mA cm下表现出令人印象深刻的12小时稳定性,始终实现高于90%的法拉第效率。通过X射线吸收、原位拉曼光谱和傅里叶变换红外光谱、理论计算以及ORR后评估,发现这种中空化合物具有固有的开放通道,其特征在于最佳的金属原子间距以及卓越的结构和组成稳定性。这些因素显著增强了2e ORR过程的热力学、动力学和稳定性。值得注意的是,所制备的化合物在中性环境中也表现出出色的2e ORR性能。此外,该策略可扩展到其他中空稀土 - P - O化合物,在中性和碱性条件下均表现出优异的2e ORR性能。