Cheng Zhaoyang, Qu Chao, Gao Chang, Kong Linghui, Yin Penggang, Lin Jianjian
Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, Shandong Key Laboratory of Biochemical Analysis, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Ministry Of Education, Qingdao, PR China.
School of Chemistry, Beihang University, Beijing, PR China.
Chemistry. 2023 Aug 4;29(44):e202300741. doi: 10.1002/chem.202300741. Epub 2023 Jul 5.
The development of cost-effective transition metal catalysts for oxygen evolution reaction (OER) is critical for the production of hydrogen fuel from water splitting. Low-cost and efficient stainless steel-based catalysts are expected to replace the scarce platinum group metals for large-scale energy applications. Here in this work, we report the conversion of commonly available inexpensive and easily accessible 434-L stainless steel (SS) into highly active and stable electrodes by corrosion and sulfuration strategies. The Ni Fe S layer as a pre-catalyst and S-doped Ni Fe oxyhydroxides in situ formed on the catalyst surface are the true active species for OER. The optimized 434-L stainless steel-based electrocatalyst exhibits a low overpotential of 298 mV at 10 mA cm in 1.0 M KOH with a small OER kinetics (the Tafel slope of 54.8 mV dec ) and good stability. This work reveals the 434-L alloy stainless steel with Fe and Cr as the main elements can be used as qualified OER catalysts by surface modification, along with a new mentality to solve the energy and resource waste problems.
开发用于析氧反应(OER)的具有成本效益的过渡金属催化剂对于通过水分解生产氢燃料至关重要。低成本且高效的不锈钢基催化剂有望取代稀缺的铂族金属用于大规模能源应用。在这项工作中,我们报道了通过腐蚀和硫化策略将常见的廉价且易于获取的434-L不锈钢(SS)转化为高活性和稳定的电极。作为预催化剂的Ni Fe S层以及在催化剂表面原位形成的S掺杂的Ni Fe羟基氧化物是OER的真正活性物种。优化后的434-L不锈钢基电催化剂在1.0 M KOH中,10 mA cm时具有298 mV的低过电位,OER动力学较小(塔菲尔斜率为54.8 mV dec)且稳定性良好。这项工作表明,以Fe和Cr为主要元素的434-L合金不锈钢通过表面改性可作为合格的OER催化剂,同时也为解决能源和资源浪费问题提供了新思路。