Surface engineering of reduced graphene oxide onto the nanoforest-like nickel selenide as a high performance electrocatalyst for OER and HER

电催化剂 塔菲尔方程 过电位 析氧 石墨烯 硒化物 化学工程 分解水 材料科学 氧化物 双功能 电化学 硫化镍 无机化学 催化作用 化学 纳米技术 电极 冶金 物理化学 有机化学 工程类 光催化
作者
Song‐Jeng Huang,Sakthipriya Balu,Nazar Riswana Barveen,Raman Sankar
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:654: 130024-130024 被引量:26
标识
DOI:10.1016/j.colsurfa.2022.130024
摘要

Developing a robust, effective, rapid and sustainable bifunctional electrocatalyst for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is highly significant to meet the requirement of the increasing energy demand. Herein, we report the successful incorporation of reduced graphene oxide (rGO) onto the hydrothermally grown nanoforest-like nickel selenide (Ni3Se2) grafted on the nickel foam (NF) via a facile dip-coating route. The fabricated Ni3Se2 shows excellent catalytic activity owing to the strong affinity of Ni3Se2 towards the NF substrate. Furthermore, the incorporation of rGO onto the Ni3Se2/NF can significantly enhance the conductivity and electrocatalytic performance of the rGO/Ni3Se2/NF electrocatalyst. The as-synthesized rGO/Ni3Se2/NF electrocatalyst exhibit a low overpotential of 292.61 mV and 251.01 mV to achieve the current density of 10 mA cm−2 (OER) and − 10 mA cm−2 (HER), respectively. The proposed rGO/Ni3Se2/NF electrocatalyst exhibit enormous active sites which in turn offers the low Tafel slope value (143.00 mV dec−1 and 134.22 mV dec−1) and enhanced electrochemical active surface area (ECSA) towards the OER and HER electrocatalytic activity in 1 M KOH solution. Furthermore, the rGO/Ni3Se2/NF electrocatalyst shows superior stability for 12 hrs with the retention rate of 99.9% and 99.8%, when operated at 10 mA cm−2 (OER) and − 10 mA cm−2 (HER), respectively. Benefitting from the synergistic action of rGO and Ni3Se2, the proposed rGO/Ni3Se2/NF electrocatalyst leads to an excellent OER and HER activity. This work offers a promising strategy for the construction of highly efficient non-precious bifunctional electrocatalyst.
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