Song Wenjiao, Xu Mingze, Teng Xue, Niu Yanli, Gong Shuaiqi, Liu Xuan, He Xiaoming, Chen Zuofeng
Shanghai Key Laboratory of Chemical Assessment and Sustainability, School of Chemical Science and Engineering, Tongji University, Shanghai 200092, China.
Nanoscale. 2021 Jan 28;13(3):1680-1688. doi: 10.1039/d0nr08395j.
In this study, we have developed intriguing self-supporting caterpillar-like spinel NiCo2S4 arrays with a hierarchical structure of nanowires on a nanosheet skeleton, which can be used as a self-supporting trifunctional electrocatalyst for the oxygen evolution reaction (OER), hydrogen evolution reaction (HER) and urea oxidation reaction (UOR). The caterpillar-like NiCo precursor arrays are first in situ grown on carbon cloth (NiCo2O4/CC) by a facile hydrothermal reaction, which is followed by an anion exchange process (or sulfuration treatment) with Na2S to form self-supporting spinel NiCo2S4 arrays (NiCo2S4/CC) with a roughened nanostructure. Taking advantage of the bimetallic synergistic effect, the unique hierarchical nanostructure, and the self-supporting nature, the resultant NiCo2S4/CC electrode exhibits high activities toward the OER, HER and UOR, which are highly superior to the monometallic counterparts of NiS nanosheets and Co9S8 nanowires on a carbon cloth substrate. The comparison of the three electrodes also indicates that the hierarchically structured bimetallic electrode combines the morphological and structural characteristics of monometallic Ni-based nanosheets and Co-based nanowires. When assembling a two-electrode electrolytic cell with NiCo2S4/CC as both the anode and cathode, an applied cell voltage of only 1.66 V is required to deliver a current density of 10 mA cm-2 in water electrolysis. By using the same two-electrode setup, the applied voltage for urea electrolysis is further reduced to 1.45 V that produces hydrogen at the cathode with the same current density. This study paves the way for exploring the feasibility of future less energy-intensive and large-scale hydrogen production.
在本研究中,我们制备了具有有趣的自支撑毛虫状结构的尖晶石型NiCo2S4阵列,其在纳米片骨架上具有纳米线的分级结构,可作为用于析氧反应(OER)、析氢反应(HER)和尿素氧化反应(UOR)的自支撑三功能电催化剂。首先通过简便的水热反应将毛虫状NiCo前驱体阵列原位生长在碳布上(NiCo2O4/CC),随后用Na2S进行阴离子交换过程(或硫化处理),以形成具有粗糙纳米结构的自支撑尖晶石型NiCo2S4阵列(NiCo2S4/CC)。利用双金属协同效应、独特的分级纳米结构和自支撑特性,所得的NiCo2S4/CC电极对OER、HER和UOR表现出高活性,这大大优于碳布基底上的NiS纳米片和Co9S8纳米线的单金属对应物。三种电极的比较还表明,分级结构的双金属电极结合了单金属Ni基纳米片和Co基纳米线的形态和结构特征。当将NiCo2S4/CC用作阳极和阴极组装两电极电解池时,在水电解中仅需施加1.66 V的电池电压即可提供10 mA cm-2的电流密度。通过使用相同的两电极装置,尿素电解的施加电压进一步降低至1.45 V,在阴极以相同电流密度产生氢气。本研究为探索未来低能耗大规模制氢的可行性铺平了道路。