In situ fabrication of low-crystallinity (Ni,Fe)xSy nanosheet arrays via room-temperature corrosion engineering toward efficient oxygen evolution

Mingyue Chen, Wenhui Li, Yu Lu, Pengcheng Qi, Hao Wu, Kunyu Hao, Yiwen Tang
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Abstract

The field of room-temperature corrosion engineering has emerged as a promising avenue for the controlled synthesis of functional nano-materials, owing to its simplicity and potential for scalability. To date, room temperature corrosion engineering has been skillfully applied and successfully used to synthesizee transition metal (oxy)hydroxides. However, the synthesis of transition metal sulfides via room-temperature corrosion encounters challenges due to the low standard electrode potential and sluggish corrosion kinetics of S/S. Here, we have successfully initiated the oxidation behavior of S on NiFe foam by adjusting the pH of the aqueous solution (containing (NH)SO and NaS), and subsequently synthesized low-crystallinity (Ni,Fe)S nanosheet arrays with significant lattice distortion and amorphous characteristics. Experimental studies combined with theoretical calculations have confirmed Fe within the (Ni,Fe)S structure functions as a highly active site while simultaneously expediting the lattice oxygen mechanism, thus yielding a remarkably efficient OER performance.
通过室温腐蚀工程原位制备低结晶度(Ni,Fe)xSy 纳米片阵列,实现高效氧气进化
室温腐蚀工程因其简便性和潜在的可扩展性,已成为受控合成功能性纳米材料的一条大有可为的途径。迄今为止,室温腐蚀工程已被熟练应用并成功用于合成过渡金属(氧)氢氧化物。然而,由于标准电极电位低和 S/S 腐蚀动力学缓慢,通过室温腐蚀合成过渡金属硫化物遇到了挑战。在此,我们通过调节水溶液(含有 (NH)SO 和 NaS)的 pH 值,成功地启动了 S 在泡沫镍铁合金上的氧化行为,随后合成了具有显著晶格畸变和无定形特征的低结晶度(Ni,Fe)S 纳米片阵列。实验研究与理论计算相结合,证实了(Ni,Fe)S 结构中的铁具有高活性位点的功能,同时加快了晶格氧机制,从而产生了显著高效的 OER 性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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