Nickel-iron oxyhydroxide (NiFeOOH) is well recognized as the best-performing oxygen evolution reaction (OER) catalyst in alkaline electrolytes, however its analogue cobalt-iron oxyhydroxide (CoFeOOH) is surprisingly less explored despite their structural similarity. Inspired by our recent study on high-performance HER catalyst using the nanostructured CoMoO•nHO precursor, herein, we report a facile synthesis of CoFeOOH catalyst derived from the same precursor and its excellent electrocatalytic properties towards the OER in alkaline electrolytes. A core-shell structured nanocatalyst consisting of disordered CoFeOOH layer over the surface of crystalline CoMoO•nHO nanosheets was synthesized using a simple hydrothermal method followed by anodic electrooxidation. Thus-prepared catalyst exhibited extraordinarily high and stable activity towards the OER in alkaline electrolyte, which outperformed most Co-based OER catalysts. Combined with the HER catalyst derived from the same CoMoO•nHO precursor as the cathode, we further developed and tested a simple water-splitting cell, which significantly surpasses the benchmarking IrO-Pt/C couple (1.63 V) and requires a voltage of only 1.517 V to afford 10 mA cm in 1.0 M KOH solution. Density functional theory calculations were conducted to gain insight into the Fe-doping induced improvement of OER activity.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919749 | PMC |
http://dx.doi.org/10.1016/j.electacta.2020.136125 | DOI Listing |
Environ Res
January 2025
School of Environment, South China Normal University, Guangzhou 510006, China; Guangdong T'echnology Research Center for Ecological Management and Remediation of Water System, Guangzhou 510006, china.
Nano zero-valent iron (nZVI) is widely used for polychlorinated biphenyl (PBDE) remediation due to its cost-effectiveness and strong reduction capacity. However, its practical application is limited by poor stability, mobility, and antioxidant performance, as well as high reactivity that leads to side reactions and activity loss. To overcome these challenges, a poly(styrene)-encapsulated nZVI (PS-nZVI) core-shell structure was developed using dispersion polymerization.
View Article and Find Full Text PDFACS Sens
January 2025
Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
It is crucial yet challenging to sensitively quantify low-abundance biomarkers in blood for early screening and diagnosis of various diseases. Herein, an analytical model of intra-mesopore immunoassay (IMIA) was proposed, which was competent to examine various biomarkers at the femtomolar level. The success is rooted in the design of an innovative superparamagnetic core-shell structure with FeO nanoparticles (NPs) at the core and hierarchically porous zeolitic imidazolate frameworks as a shell (FeO@HPZIF-8), achieved through a soft-template directed self-assembly coupled with confinement growth mechanism.
View Article and Find Full Text PDFSmall
January 2025
Key Laboratory of Aerospace Materials and Performance (Ministry of Education) School of Materials Science and Engineering, Beihang University, No.37 Xueyuan Road, Beijing, 100191, P. R. China.
A reasonable construction of hollow structures to obtain high-performance absorbers is widely studied, but it is still a challenge to select suitable materials to improve the low-frequency attenuation performance. Here, the FeO@C@NiO nanoprisms with unique tip shapes, asymmetric multi-path hollow cavity, and core-shell heteroepitaxy structure are designed and synthesized based on anisotropy and intrinsic physical characteristics. Impressively, by changing the load of NiO, the composites achieve strong absorption, broadband, low-frequency absorption: the reflection loss of -55.
View Article and Find Full Text PDFAdv Mater
January 2025
Department of Materials Science and Engineering, Institute of Innovative Materials (I2, M), Shenzhen Key Laboratory of Full Spectral Solar Electricity Generation (FSSEG), Southern University of Science and Technology (SUSTech), No. 1088, Xueyuan Rd., Shenzhen, Guangdong, 518055, China.
Mutual acquisition of phase-stability and controllable phase-transition becomes a predominant criterion of phase-change materials for the practical long-term energy storage but seems contradictory always. Here a strategy combining coordination and hydrogen bonds hierarchically to create a supercooled liquid in a core-shell coordination structure is reported, addressing that demand successfully. This new material is composed of a Mn-methylurea complex (MM) core and the hierarchically bonded erythritols shell.
View Article and Find Full Text PDFChem Sci
January 2025
Interdisciplinary Research Center for Sustainable Energy Science and Engineering (IRC4SE2), School of Chemical Engineering, Zhengzhou University Henan 450001 China
The exceptional oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) performances of core-shell catalysts are well documented, yet their activity and durability origins have been interpreted only based on the static structures. Herein we employ a NiFe alloy coated with a nitrogen-doped graphene-based carbon shell (NiFe@NC) as a model system to elucidate the active structure and stability mechanism for the ORR and OER by combining constant potential computations, molecular dynamic simulations, and experiments. The results reveal that the synergistic effects between the alloy core and carbon shell facilitate the formation of Fe-N-C active sites and replenish metal sites when central metal atoms detach.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!