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三相NiP-NiP@NiS体系中的协同调制表现出显著的全水解性能。

Synergistic modulation in a triphasic NiP-NiP@NiS system manifests remarkable overall water splitting.

作者信息

Pundir Vikas, Gaur Ashish, Kaur Rajdeep, Sharma Jatin, Kumar Rajinder, Bagchi Vivek

机构信息

Institute of Nano Science and Technology, Sector-81, Knowledge City, Sahibzada Ajit Singh Nagar, Punjab 140306, India.

Institute of Nano Science and Technology, Sector-81, Knowledge City, Sahibzada Ajit Singh Nagar, Punjab 140306, India.

出版信息

J Colloid Interface Sci. 2023 Dec;651:579-588. doi: 10.1016/j.jcis.2023.07.112. Epub 2023 Jul 22.

Abstract

The potential for water splitting electrocatalysts with high efficiency paves the way for a sustainable future in hydrogen energy. However, this task is challenging due to the sluggish kinetics of the oxygen evolution reaction (OER), which has a significant impact on the hydrogen evolution reaction (HER). Herein multi-heterointerface of NiP-NiP@NiS was fabricated by a two-step synthesis procedure that consist the development of NiP-NiP nanosheets over nickel foam followed by the electrodeposition of NiS. The HR-TEM analysis shows that the NiP-NiP@NiS nanosheets array provide numerous well-exposed diverse heterointerfaces. The electrochemical investigations conducted on the NiP-NiP@NiS nanosheets for complete water splitting indicate that they possess an overpotential of 73 mV and 230 mV in HER and OER respectively, enabling them to generate a current density of 10 and 50 mA cm. The nanosheets also demonstrate Tafel slope values of 95 mV dec and 83 mV dec for HER and OER, respectively. The HER stability of the catalyst was conducted for 45 h using chronoamperometric technique under a current density of 20 mA cm, while the stability test for OER was carried out at current densities of 100 and 200 mA cm for 100 h each. Furthermore, in the overall water splitting, the catalyst exhibits a cell voltage of 1.47 V@10 mA cm and displayed a stability operation for 100 h at a current density of 150 mA cm.

摘要

高效的水分解电催化剂的潜力为氢能的可持续未来铺平了道路。然而,由于析氧反应(OER)动力学缓慢,这项任务具有挑战性,析氧反应对析氢反应(HER)有重大影响。在此,通过两步合成法制备了NiP-NiP@NiS的多异质界面,该方法包括在泡沫镍上生长NiP-NiP纳米片,然后电沉积NiS。高分辨透射电子显微镜(HR-TEM)分析表明,NiP-NiP@NiS纳米片阵列提供了大量充分暴露的不同异质界面。对用于完全水分解的NiP-NiP@NiS纳米片进行的电化学研究表明,它们在析氢反应和析氧反应中的过电位分别为73 mV和230 mV,能够产生10和50 mA cm的电流密度。这些纳米片在析氢反应和析氧反应中的塔菲尔斜率值分别为95 mV dec和83 mV dec。使用计时电流法在20 mA cm的电流密度下对催化剂的析氢反应稳定性进行了45小时的测试,而对析氧反应的稳定性测试则在100和200 mA cm的电流密度下分别进行了100小时。此外,在整体水分解中,该催化剂在10 mA cm时的电池电压为1.47 V,并在150 mA cm的电流密度下稳定运行了100小时。

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