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在还原氧化石墨烯包覆的泡沫镍上生长的坚固FeCoP纳米颗粒,作为用于优异碱性和海水电解的高效析氧催化剂。

Robust FeCoP nanoparticles grown on a rGO-coated Ni foam as an efficient oxygen evolution catalyst for excellent alkaline and seawater electrolysis.

作者信息

Zheng Yingping, Yu Dehua, Xu Wei, Zhang Ke, Ma Kaili, Guo Xinyu, Lou Yongbing, Hu Mulin

机构信息

School of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, China.

Analysis and Testing Center, Southeast University, Nanjing 211189, P. R. China.

出版信息

Dalton Trans. 2023 Mar 14;52(11):3493-3500. doi: 10.1039/d2dt03857a.

Abstract

Electrochemical water splitting is a potential green hydrogen energy generation technique. With the shortage of fresh water, abundant seawater resources should be developed as the main raw material for water electrolysis. However, since the precipitation reaction of chloride ions in seawater will compete with the oxygen evolution reaction (OER) and corrode the catalyst, seawater electrolysis is restricted by the decrease in activity, low stability, and selectivity. Rational design and development of efficient and stable catalysts is the key to seawater electrolysis. Herein, a high-activity bimetallic phosphide FeCoP, grown on a reduced graphene oxide (rGO)-protected Ni Foam (NF) substrate using FeCo Prussian Blue Analogue (PBA) as a template, was designed for application in alkaline natural seawater electrolysis. The OER activity confirmed that the formed FeCoP@rGO/NF has high electrocatalytic performance. In 1 M KOH and natural alkaline seawater, the overpotential was only 257 mV and 282 mV under 200 mA cm, respectively. It also demonstrated long-term stability up to 200 h. Therefore, this study provides new insight into the application of PBA as a precursor of bimetallic phosphide in the electrolysis of seawater at high current density.

摘要

电化学水分解是一种潜在的绿色氢能生成技术。随着淡水短缺,应开发丰富的海水资源作为水电解的主要原料。然而,由于海水中氯离子的沉淀反应会与析氧反应(OER)竞争并腐蚀催化剂,海水电解受到活性降低、稳定性差和选择性低的限制。合理设计和开发高效稳定的催化剂是海水电解的关键。在此,以FeCo普鲁士蓝类似物(PBA)为模板,在还原氧化石墨烯(rGO)保护的泡沫镍(NF)基底上生长出一种高活性双金属磷化物FeCoP,用于碱性天然海水电解。OER活性证实所形成的FeCoP@rGO/NF具有高电催化性能。在1 M KOH和天然碱性海水中,在200 mA cm下过电位分别仅为257 mV和282 mV。它还展示了长达200 h的长期稳定性。因此,本研究为PBA作为双金属磷化物前驱体在高电流密度海水电解中的应用提供了新的见解。

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