Synergistic modulation in a triphasic Ni5P4-Ni2P@Ni3S2 system manifests remarkable overall water splitting

塔菲尔方程 析氧 过电位 分解水 电化学 催化作用 电流密度 化学工程 材料科学 化学 电极 物理化学 冶金 生物化学 物理 光催化 量子力学 工程类
作者
Vikas Pundir,Ashish Gaur,Rajdeep Kaur,Jatin Sharma,Rajinder Kumar,Vivek Bagchi
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:651: 579-588 被引量:14
标识
DOI:10.1016/j.jcis.2023.07.112
摘要

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 Ni5P4-Ni2P@Ni3S2 was fabricated by a two-step synthesis procedure that consist the development of Ni5P4-Ni2P nanosheets over nickel foam followed by the electrodeposition of Ni3S2. The HR-TEM analysis shows that the Ni5P4-Ni2P@Ni3S2 nanosheets array provide numerous well-exposed diverse heterointerfaces. The electrochemical investigations conducted on the Ni5P4-Ni2P@Ni3S2 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−2. The nanosheets also demonstrate Tafel slope values of 95 mV dec−1 and 83 mV dec−1 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−1, while the stability test for OER was carried out at current densities of 100 and 200 mA cm−1 for 100 h each. Furthermore, in the overall water splitting, the catalyst exhibits a cell voltage of 1.47 V@10 mA cm−2 and displayed a stability operation for 100 h at a current density of 150 mA cm−1.
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