Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Nowadays, exploring efficient electrocatalysts is crucial for the tri-functional oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). In this study, we designed a novel electrocatalyst based on Mn- and B-doped Co-glycerate@cobalt carbonate hydroxide for the tri-functional OER, HER and ORR under alkaline conditions. Electrochemical measurements demonstrate overpotentials of 318 and 75 mV at a current density of 10 mA cm for the OER and HER, respectively. Moreover, a two-electrode device based on the prepared electrocatalyst required low cell voltages of 1.61 V and 1.86 V to achieve current densities of 10 and 100 mA cm, respectively. The prepared electrocatalyst exhibits an onset potential of 0.96 V and a half-wave potential of 0.89 V as a robust electrocatalyst for the ORR. The improved electrocatalytic performance of the prepared electrocatalyst can be attributed to the increased electrical conductivity enabled by heteroelement doping and synergistic effects.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d5nr02150bDOI Listing

Publication Analysis

Top Keywords

prepared electrocatalyst
12
co-glycerate@cobalt carbonate
8
carbonate hydroxide
8
evolution reaction
8
electrocatalyst
5
orr
4
orr oer
4
oer activity
4
activity promotion
4
promotion hierarchical
4

Similar Publications

Transient mixed-valent Ni active sites boost urea electrooxidation.

J Colloid Interface Sci

September 2025

Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei 230026, China; Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, China. Electronic address:

The utilization of synergistic multivalent active sites holds potential in addressing the inherent sluggish kinetics of electrocatalytic reactions. Herein, we prepared au uNPs/Ni-NDC (NDC = 1,4-Naphthalenedicarboxylic acid) and leveraged the localized surface plasmon resonance (LSPR) effect to drive hot electron transfer from au nanoparticles to the Ni substrate, thereby generating multivalent active sites to boost the urea oxidation reaction (UOR). Under exciting light, au uNPs/Ni-NDC exhibited a twofold increase in UOR current accompanied by a significant negative shift in onset potential.

View Article and Find Full Text PDF

The oxygen reduction reaction (ORR) is critical to energy conversion technologies and requires efficient catalysts for superior performance. Herein, nitrogen-doped carbide-derived carbon (N-CDC) catalysts are prepared using novel engineered molecular architectures based on polymer-derived ceramic technology. The obtained catalyst materials show a surface N concentration of >5 wt % and a hierarchically porous structure, resulting in a specific surface area of over 2000 m g.

View Article and Find Full Text PDF

The rational design of electrode materials with outstanding energy and power density for supercapacitors (SCc) and high-performance electrocatalysts in alkaline media plays an indispensable role in the application of energy storage and overall water splitting. In this paper, we prepared NiCoFe layered ternary hydroxides (LTH) using a hydrothermal synthesis method. The sample with a Ni/Co/Fe ratio of 1:2:0.

View Article and Find Full Text PDF

Water electrolysis for hydrogen production has become an industrial focus in the era of green chemistry due to its high purity of hydrogen production and environmentally friendly, efficient process. As the half reaction of water splitting at the anode, the oxygen evolution reaction (OER) features a complex and sluggish process that restricts the efficiency of water splitting. The mechanism of OER varies with different electrolytes.

View Article and Find Full Text PDF

Influence of the Metal Support─Catalyst Contact on the Performance of NiO-Based O Evolution Electrocatalysts.

ACS Appl Mater Interfaces

September 2025

Surface Science Laboratory, Department of Materials and Geosciences, Technical University of Darmstadt, Peter-Grünberg-Straße 4, 64287 Darmstadt, Germany.

The performance of NiO-based electrocatalysts for the oxygen evolution reaction (OER) is strongly influenced by the interface between the metal support (current collector) and the catalyst layer, which modulates electronic properties and electrochemical activity. This study systematically investigates the solid-solid interface behavior of NiO thin films prepared by reactive magnetron sputtering on Pt, Au, and Ni, followed by electrochemical characterization. Stepwise NiO deposition and X-ray photoelectron spectroscopy reveal distinct band alignment and electronic structure differences at the metal-catalyst interface.

View Article and Find Full Text PDF