材料科学
过电位
异质结
电解
电催化剂
析氧
分解水
电解水
法拉第效率
化学工程
海水
电化学
纳米技术
光电子学
催化作用
电极
光催化
物理化学
海洋学
地质学
工程类
电解质
生物化学
化学
作者
Manoj Bollu,Duy Thanh Tran,Sampath Prabhakaran,Do Hwan Kim,Nam Hoon Kim,Joong Hee Lee
出处
期刊:Nano Energy
[Elsevier]
日期:2024-02-20
卷期号:123: 109413-109413
被引量:11
标识
DOI:10.1016/j.nanoen.2024.109413
摘要
For the generation of renewable hydrogen via water electrolysis, it is necessary to develop electrocatalysts with high performance and maximum metal utilization. Herein, we report an effective electrocatalyst of interconnected nanonetwork based on one-dimensional CoNi@CoNiP heterostructures implanted with ultralow loading of platinum single atoms (CN@CNP-Pt). Our study indicates that the CN@CNP-Pt could promote hydrogen evolution reaction (HER) with an overpotential (η) of 22 (75) mV, while the CN@CNP counterpart requires η of 198 (291) mV for oxygen evolution reaction (OER) at 10 (100) mA cm-2 in alkaline medium. The two-electrode electrolyzer of CN@CNP-Pt(-)//CN@CNP(+) drives a small cell voltage of 1.49 V (1.51) at 75 oC to accomplish 10 mA cm-2 towards freshwater (seawater) splitting, superior to the corresponding values of Pt/C(-)//RuO2(+) unit and other materials featured in early reports. The advantages of CN@CNP-Pt(-)//CN@CNP(+) are also confirmed via the excellent mass activity about 15.7 times higher than that of commercial Pt/C(–)//RuO2(+). The CN@CNP heterostructures produces a large active surface area, multiple active sites, and excellent charge transfer. Further, implanting Pt atoms into CN@CNP surface significantly modifies the electronic structure to result in favorable free adsorption energy, thus achieving potential electrocatalysts with enhanced activity for economic and sustainable freshwater/seawater splitting.
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