The upgraded performance of the NiFe2O4 /C electrocatalyst using Co substitution for the oxygen reduction reaction in an alkaline solution

被引:7
作者
Matseke, Mphoma S. [1 ,2 ]
Luo, Hongze [1 ]
Wen, Lei [3 ]
Zheng, Haitao [1 ]
机构
[1] CSIR, Energy Ctr, POB 395, ZA-0001 Pretoria, South Africa
[2] Univ Johannesburg, Dept Chem Sci, POB 524, ZA-2006 Johannesburg, South Africa
[3] Chinese Acad Sci, Inst Met Res IMR, 72 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
基金
新加坡国家研究基金会;
关键词
Spinel; Co; Substitution; ORR; NiFe2O4; BI-FUNCTIONAL ELECTROCATALYSTS; SPINEL NIFE2O4; NANOPARTICLES; GRAPHENE; FERRITE; NANOSPHERES; CATALYSTS; SHEETS;
D O I
10.1016/j.jpcs.2022.110644
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
NiFe2O4 is one of the most abundant and inexpensive spinels; however, its activity toward the oxygen reduction reaction (ORR) is relatively low. For the first time, Co-substituted Fe partly of the NiFe2O4 electrocatalyst was studied to improve the intrinsic activity of ORR. Spinel-type NiFe2-xCoxO4/C electrocatalysts (x = 0, 0.25, 0.5 and 0.75) were synthesized by the hydrothermal method without further calcination. The well-crystallized NiFe2O4/C nanoparticles remained in a single phase after Co-substituting with sizes of 15-20 nm, characterized by TEM, SEM, XRD, and FTIR. XPS observes mixed valence states in the NiFe2-xCoxO4/C structure are observed, which has a beneficial effect on ORR. Furthermore, NiFe2-xCoxO4/C nanoparticles (x = 0.25, 0.5 and 0.75) show advanced ORR performance over NiFe2O4, particularly, the specific mass activity of NiFe1.75Co0.25O4/C is three times higher than that of NiFe2O4, also, with improved stability. After 4,000s, the NiFe1.75Co0.25O4/C electrocatalyst retained 84% of its initial current density, while the NiFe2O4/C electrocatalyst retained only 38%. The results revealed that Co substitutions have remarkably increased the intrinsic activity of the NiFe2O4 electrocatalyst for ORR by altering the structure, redistributing cations, and improving electrical conductivity.
引用
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页数:7
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