journal article·2025-02-24

NiSe2-Nanooctahedron as an Efficient Electrocatalyst for Overall Water Splitting

Amit Kumar Nayak, Debabrata Pradhan

ACS Applied Energy Materials· Volume 8· Issue 4
Publisher page

Abstract

Hydrogen production through electrocatalysis has attracted much attention due to negligible environmental pollution by using renewable electrical energy. To bring electrolysis technology to cost parity, a nonprecious, stable, and earth-abundant transition-metal-based bifunctional catalyst is desired for overall water splitting. Herein, we report the synthesis of NiSe 2 nanoparticles using a simple, template-free, and single-step solvothermal method by varying the reaction medium, i.e., either water or propanol or their mixture. Using the ethylenediaminetetraacetic acid (EDTA) as a structure-directing agent, nanooctahedron-shaped NiSe 2 particles are synthesized for the first time. The nanosized NiSe 2 octahedron is demonstrated as a potential bifunctional electrocatalyst for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in an alkaline medium. For hydrogen evolution, a small overpotential of 119 mV is needed to generate a current density of 10 mA cm –2, whereas 345 mV overpotential is required for oxygen evolution reaction delivering a current density of 50 mA cm –2 . Furthermore, the electrolyzer with NiSe 2 -nanooctahedrons as an electrocatalyst delivers 10 mA cm –2 at a cell voltage of 1.55 V for overall water splitting and shows excellent stability with a negligible change in current density in 20 h.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Materials Science Centre

Indian Institute of Technology

Funding

Council of Scientific and Industrial Research, India · Science and Engineering Research Board

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