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高效氧载体 NiFeP(oxy)羟基纳米粒子嵌入生物废料衍生的氮掺杂多孔碳中,用于双功能电催化剂。

Highly efficient oxygen carrier NiFeP (oxy) hydroxides nanoparticle embedded in N-doped porous carbon derived from bio-waste for bifunctional electrocatalysts.

机构信息

Graduate Institute of Environmental Engineering, National Central University, Taiwan No. 300, Chung-Da Road., Chung-Li District, Tao-Yuan City 32001, Taiwan.

Graduate Institute of Environmental Engineering, National Central University, Taiwan No. 300, Chung-Da Road., Chung-Li District, Tao-Yuan City 32001, Taiwan.

出版信息

Chemosphere. 2024 Oct;366:143486. doi: 10.1016/j.chemosphere.2024.143486. Epub 2024 Oct 12.

Abstract

Developing cost-effective, readily available materials for efficient hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in water splitting is a crucial step toward enhancing the profitability and sustainability of energy conversion systems. This research introduces a novel synthesis method for NiFeP/NPC OHs from banana peel bio-waste, a method that could revolutionize the field of materials science and electrochemistry. The use of metallic phosphides, known for their excellent electrical conductivity and catalytic activity, as bifunctional catalysts, combined with the efficient synthesis of nanoporous carbons (NPC) from banana peel bio-waste (BPW), could pave the way for a new era of sustainable and cost-effective energy conversion. By chemically activating different porogens, such as nickel, iron, and phosphorus (NiFeP), to form (oxy) hydroxides (OHs), functional carbonaceous structures with a high density of pores and large specific surface areas can be achieved. The resulting materials, designated as NiFeP/NPC OHs, are characterized by their remarkable porosity, high conductivity, large surface area, and chemical stability. These properties make NiFeP/NPC OHs particularly suitable for electrocatalysis, where they exhibit outstanding activity in both HER and OER. The optimized NiFeP/NPC OHs material shows a very low overpotential of 93 mV for HER and 243 mV for OER at 10 mA cm⁻ and high durability over 100 h. Moreover, the bifunctional NiFeP/NPC OHs electrode demonstrates exceptional catalytic activity and stability in alkaline solutions. This study not only highlights the innovative synthesis of NPC from BPW and the cost-effective fabrication of NiFeP/NPC OHs but also sparks curiosity about the potential of this novel synthesis method.

摘要

开发具有成本效益、易于获得的材料,以促进水分解中的高效析氢反应(HER)和析氧反应(OER),是提高能源转换系统盈利能力和可持续性的关键步骤。本研究介绍了一种从香蕉皮生物废料中合成 NiFeP/NPC OHs 的新方法,这种方法可能会彻底改变材料科学和电化学领域。使用金属磷化物作为双功能催化剂,它们具有优异的导电性和催化活性,与从香蕉皮生物废料(BPW)高效合成纳米多孔碳(NPC)相结合,为可持续和具有成本效益的能源转换开辟了新纪元。通过化学激活不同的造孔剂,如镍、铁和磷(NiFeP),形成(氧)氢氧化物(OHs),可以获得具有高密度孔和大比表面积的功能性碳质结构。所得材料被指定为 NiFeP/NPC OHs,其特点是具有显著的多孔性、高导电性、大比表面积和化学稳定性。这些特性使 NiFeP/NPC OHs 特别适合电催化,在 HER 和 OER 中均表现出出色的活性。优化后的 NiFeP/NPC OHs 材料在 10 mA cm⁻²时 HER 的过电位仅为 93 mV,OER 的过电位为 243 mV,并且具有超过 100 小时的高耐久性。此外,双功能 NiFeP/NPC OHs 电极在碱性溶液中表现出出色的催化活性和稳定性。本研究不仅突出了从 BPW 中合成 NPC 的创新性和 NiFeP/NPC OHs 的成本效益制造,还激发了人们对这种新型合成方法的兴趣。

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