Key Laboratory of Sensor Analysis of Tumor Marker Ministry of Education, State Key Lab Base of Eco-chemical Engineering, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Dalton Trans. 2018 Oct 30;47(42):14917-14923. doi: 10.1039/c8dt02927j.
Exploration and fabrication of low-cost but highly active electrocatalysts, alternatives to noble metals, have remained a challenge for overall water splitting reaction. To date, few studies have reported that the Earth-abundant pyrite FeS2 is catalytically active for hydrogen evolution reaction, while there is no study on the oxygen evolution reaction and overall water splitting reaction using pyrite FeS2 as an electrocatalyst. Here, we offer a facile hydrothermal approach for the synthesis of FeS2 nanoparticles by the reduction of FeCl3·6H2O with C5H10NS2Na·3H2O. The FeS2/C nanoparticles on Ni foam (NF) deliver 10 mA cm-2 at an overpotential of 240 mV towards the oxygen evolution reaction, which is lower than that of IrO2. It requires 202 mV to drive the hydrogen evolution reaction to reach 10 mA cm-2, while long-term durability and faster charge-transfer kinetics confirm the good hydrogen evolution reaction performance on FeS2/C/Ni foam. Moreover, the pyrite FeS2/C/nanoparticles on Ni foam are assembled as an anode and cathode in a two-electrode alkaline electrolyzer and show good overall water splitting efficiency with 1.72 V at 10 mA cm-2.
探索和制造低成本但高活性的电催化剂,替代贵金属,一直是整体水分解反应的一个挑战。迄今为止,很少有研究报道自然界中丰富的黄铁矿 FeS2 对析氢反应具有催化活性,但没有研究报道使用黄铁矿 FeS2 作为电催化剂进行析氧反应和整体水分解反应。在这里,我们提供了一种简便的水热方法,通过 C5H10NS2Na·3H2O 还原 FeCl3·6H2O 合成 FeS2 纳米粒子。在碱性条件下,FeS2/C 纳米粒子在 NF 上的析氧反应过电位为 240 mV 时可达到 10 mA cm-2,低于 IrO2。它需要 202 mV 的过电位来驱动析氢反应达到 10 mA cm-2,而长期的耐久性和更快的电荷转移动力学证实了 FeS2/C/Ni 泡沫在析氢反应上的良好性能。此外,黄铁矿 FeS2/C 纳米粒子在 NF 上组装成一个两电极碱性电解槽的阳极和阴极,在 10 mA cm-2 时,以 1.72 V 的电压表现出良好的整体水分解效率。