In-situ confinement growth of FeNi alloy within B/N co-doped carbon nanotubes as efficient electrocatalyst for water splitting

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL
Shide Wu , Yapeng Li , Dan Ping , Weitao Liu , Yichen Feng , Qingshuo Zhang , Mengjin Gao , Shuqing Liu , Di Wu , Shiwen Wang , Jianqiang Zhang , Shaoming Fang
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引用次数: 0

Abstract

Developing low-cost and efficient catalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) still remains a challenge in water electrolysis. Herein, FeNi alloy encapsulated within boron and nitrogen co-doped carbon (FeNi@BNC) nanotubes are synthesized through a simple one-step pyrolysis method using FeCl3·6H2O, NiCl2·6H2O, H3BO3, urea and PEG-2000 as precursors. The BNC nanotubes are quite requisite for dispersing and stabilizing FeNi alloy nanoparticles (NPs) during pyrolysis. Benefiting from the synergistic catalytic effect of Fe and Ni, as well as the confinement effect of BNC nanotubes, such FeNi@BNC catalyst demonstrates impressive activities for both HER and OER, much superior to pristine Fe@BNC and Ni@BNC. Notably, the overpotentials needed to achieve a current density of 10 mA·cm−2 are just 230 mV for HER and 280 mV for OER. Moreover, the FeNi@BNC catalyst demonstrates significant stability, showing no noticeable degradation during potentiostatic electrolysis or repeated CV tests. Furthermore, FeNi@BNC exhibits remarkable activity for overall water splitting, requiring cell voltages of just 1.24 V and 1.60 V vs. RHE to achieve current densities of 10 mA·cm−2 and 20 mA·cm−2, respectively. This study introduces a novel strategy for developing bifunctional electrocatalysts with high-efficiency water splitting performance.

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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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