Highly Porous Carbon Flakes Derived from Cellulose and Nickel Phosphide Heterostructure towards Efficient Electrocatalysis of Oxygen Evolution Reaction

磷化物 电催化剂 析氧 材料科学 化学工程 碳纤维 纤维素 电化学 交换电流密度 碳化 复合数 化学 塔菲尔方程 复合材料 冶金 电极 物理化学 工程类 扫描电子显微镜
作者
Ewa Mijowska,Karolina Pietrusewicz,Klaudia Maślana
出处
期刊:Molecules [Multidisciplinary Digital Publishing Institute]
卷期号:29 (2): 352-352 被引量:5
标识
DOI:10.3390/molecules29020352
摘要

This study delves into the pressing challenges of climate change and the escalating carbon dioxide (CO2) emissions by exploring hydrogen technology as a sustainable alternative. In particular, there is focus on nickel phosphide-based electrocatalysts, known for their promising performance in hydrogen evolution reactions (HERs) and oxygen evolution reactions (OERs). Therefore, here we have designed a facile strategy to deliver highly porous carbon flakes derived from cellulose fibers via carbonization at 850 °C, yielding highly porous structures and outstanding specific surface area (SSAcel_carb_850_act = 3164 m2/g) after activation. As-fabricated carbon was utilized as a support for Ni12P5 with an optimized mass ratio. Electrochemical testing revealed that the composite of Ni12P5 and carbon flakes with a ratio of 100:1, respectively, exhibited the most favorable kinetics for the oxygen evolution reaction (OER). Importantly, the durability tests of this sample demonstrated the most stable behavior and lowest potential change under high current density among the studied samples, making it a promising candidate in practical applications. Moreover, the analysis of electrocatalysts after an OER does not show any changes, indicating that the sample does not undergo undesired intermediate reactions and that unwanted products are not released, explaining its stable behavior. This provides a straightforward approach for creating a cellulose-derived composite with enhanced electroactivity and durability.
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