Liu Liangbin, Ji Yujin, You Wentao, Liu Shangheng, Shao Qi, Kong Qingyu, Hu Zhiwei, Tao Huabing, Bu Lingzheng, Huang Xiaoqing
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, P. R. China.
Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Jiangsu, 215123, P. R. China.
Small. 2023 Sep;19(38):e2208202. doi: 10.1002/smll.202208202. Epub 2023 May 24.
Pursuing highly active and long-term stable ruthenium (Ru) based oxygen evolution reaction (OER) catalyst for water electrolysis under acidic conditions is of great significance yet a tremendous challenge to date. To solve the problem of serious Ru corrosion in an acid medium, the trace lattice sulfur (S) inserted RuO catalyst is prepared. The optimized catalyst (Ru/S NSs-400) has shown a record stability of 600 h for the solely containing Ru (iridium-free) nanomaterials. In the practical proton exchange membrane device, the Ru/S NSs-400 can even sustain more than 300 h without obvious decay at the high current density of 250 mA cm . The detailed investigations reveal that S doping not only changes the electronic structure of Ru via forming RuS coordination for high adsorption of reaction intermediates but also stabilizes Ru from over-oxidation. This strategy is also effective for improving the stability of commercial Ru/C and homemade Ru-based nanoparticles. This work offers a highly effective strategy to design high-performance OER catalysts for water splitting and beyond.
在酸性条件下寻找用于水电解的高活性、长期稳定的钌(Ru)基析氧反应(OER)催化剂具有重要意义,但迄今为止仍是一项巨大挑战。为了解决Ru在酸性介质中严重腐蚀的问题,制备了微量晶格硫(S)插入的RuO催化剂。优化后的催化剂(Ru/S NSs-400)在仅含Ru(无铱)的纳米材料中表现出创纪录的600小时稳定性。在实际的质子交换膜装置中,Ru/S NSs-400在250 mA cm的高电流密度下甚至可以持续运行300多个小时而无明显衰减。详细研究表明,S掺杂不仅通过形成Ru-S配位改变Ru的电子结构以实现对反应中间体的高吸附,还能使Ru免于过度氧化。该策略对于提高商业Ru/C和自制Ru基纳米颗粒的稳定性也有效。这项工作为设计用于水分解及其他领域的高性能OER催化剂提供了一种高效策略。