Synchronously integration of Co, Fe dual-metal doping in Ru@C and CDs for boosted water splitting performances in alkaline media

分解水 材料科学 对偶(语法数字) 催化作用 兴奋剂 金属 无机化学 光电子学 化学 冶金 光催化 生物化学 文学类 艺术
作者
Mingxi Yang,Tanglue Feng,Yixin Chen,Junjun Liu,Xiaohuan Zhao,Bai Yang
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:267: 118657-118657 被引量:99
标识
DOI:10.1016/j.apcatb.2020.118657
摘要

• CoFeRu@C and CoFe-CDs with different electrocatalytic functions were simultaneously synthesized within one-pot hydrothermal reactor. • Synergistic effect of Co, Fe co-doping in CDs and Ru@C effectively improved the charge transfer and electrocatalytic activities . • CoFeRu@C exhibited the lowest HER overpotential of 4 mV in 1 M KOH among all the reported noble- and non-noble metal-based HER electrocatalysts . • Based on CoFe-CDs/CoFeRu@C system only 1.59 V was needed to achieve 10 mA cm -2 for electrochemical overall water-splitting in alkaline media. The unsatisfactory performances and complicated synthesis procedures greatly impeded the large-scale industrial applications of various electrocatalysts . Herein, two different functional electrocatalysts were simultaneously synthesized within one-pot reactor through hydrothermal method. The Co, Fe co-doped carbon dots (CoFe-CDs) with electrocatalytic oxygen evolution reaction (OER) activities and carbon-supported Co, Fe co-doped Ru networks (CoFeRu@C) with hydrogen evolution reaction (HER) activities, were directly obtained from the supernatant and the precipitation, respectively. Benefiting from the synergistic effect of dual-metal doping, the CoFeRu@C exhibited an extremely low overpotential of 4 mV for HER in 1 M KOH electrolyte, which was the lowest value among the previously reported electrocatalysts, and the CoFe-CDs showed excellent OER performance with an overpotential of 320 mV. Moreover, only 1.59 V was needed to achieve 10 mA cm −2 for overall water-splitting. This work provided an innovative approach for simply creating diverse electrocatalysts and effectively regulating the catalytic activities by introducing multi-metal dopants.
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