电催化剂
电解水
电解
制氢
海水
电化学
化学工程
氢
碳纤维
材料科学
分解水
化学
无机化学
纳米技术
催化作用
电极
物理化学
复合材料
电解质
有机化学
复合数
海洋学
工程类
地质学
光催化
作者
Subramanian Vijayapradeep,Natarajan Logeshwaran,S. Ramakrishnan,Ae Rhan Kim,Sampath Prabhakaran,Do Hwan Kim,Dong Jin Yoo
标识
DOI:10.1016/j.cej.2023.145348
摘要
Electrochemical water electrolysis is a prominent method of green-hydrogen fuel production. Tailored nanostructures of Pt-based electrocatalysts have high priority in hydrogen production. Herein, we fabricated carbon-encapsulated Pt core–shell supported CoMo2S4-NGNF as an efficient electrocatalyst for the hydrogen evolution reaction (HER). The novel carbon-encapsulated Pt core shells improved the long-term durability. The Pt@CoMo2S4-NGNF hybrids displayed overpotentials of 27 mV to achieve a current density of 10 mA cm−2 in 1.0 M KOH and outstanding durability of 100 h. When Pt@CoMo2S4-NGNF∥IrO2 was employed in overall seawater electrolysis applications, it required 1.54 V to achieve a 10 mA cm−2 current density. Additionally, we evaluated the electronic structure and HER mechanism of Pt@CoMo2S4 & CoMo2S4 using density functional theory (DFT) calculations. This work illustrates the possibility of designing an effective, long-lasting, and scalable electrocatalyst for the electrolysis of alkaline and seawater to produce pure hydrogen.
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