Electrocatalytic Potential of Borophene Derivatives in the Oxygen Evolution Reaction

Since borophene and its derivatives exhibit a wide variety of phases, universal fabrication routes have not yet been fully established. In this study, we present a liquid-phase chemical exfoliation method for borophene using acids and oxidants. Unlike the Hummers method for graphite, this approach enables the exfoliation of boron without inducing oxidation. Oxygen species were incorporated by treating the flakes under a hydrogen atmosphere at different temperatures, with changes monitored by X-ray photoelectron spectroscopy (XPS). The B–O/B–B bonding ratio was tuned, and the formation of B2O3 was detected. Higher-temperature treatments introduced defects and holes, as confirmed by TEM, which, in turn, provided active sites for electrocatalysis. Borophene treated at 600 °C in hydrogen proved highly active and durable in the oxygen evolution reaction (OER), achieving a Tafel slope of 100 mV/dec and an electrochemical active surface area (ECSA) of 46 m2/g. Postmortem studies of the sample by means of XPS identified active intermediates, highlighting the borophene potential as a novel metal-free electrocatalyst. This research shows borophene derivaties fabrication and its compositional and morphological tuning for catalytic applications.

Authors

Institutions

Publication Details

Journal
The Journal of Physical Chemistry C
Published
2026-01-06
DOI
https://doi.org/10.1021/acs.jpcc.5c04377
Primary Topic
Boron and Carbon Nanomaterials Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Electrocatalytic Potential of Borophene Derivatives in the Oxygen Evolution Reaction

Klaudia Maślana, Ewa Mijowska, Krzysztof Sielicki
The Journal of Physical Chemistry C
Boron and Carbon Nanomaterials Research
article

Electrocatalytic Potential of Borophene Derivatives in the Oxygen Evolution Reaction

Klaudia Maślana, Ewa Mijowska, Krzysztof Sielicki
article en

Abstract

Since borophene and its derivatives exhibit a wide variety of phases, universal fabrication routes have not yet been fully established. In this study, we present a liquid-phase chemical exfoliation method for borophene using acids and oxidants. Unlike the Hummers method for graphite, this approach enables the exfoliation of boron without inducing oxidation. Oxygen species were incorporated by treating the flakes under a hydrogen atmosphere at different temperatures, with changes monitored by X-ray photoelectron spectroscopy (XPS). The B–O/B–B bonding ratio was tuned, and the formation of B2O3 was detected. Higher-temperature treatments introduced defects and holes, as confirmed by TEM, which, in turn, provided active sites for electrocatalysis. Borophene treated at 600 °C in hydrogen proved highly active and durable in the oxygen evolution reaction (OER), achieving a Tafel slope of 100 mV/dec and an electrochemical active surface area (ECSA) of 46 m2/g. Postmortem studies of the sample by means of XPS identified active intermediates, highlighting the borophene potential as a novel metal-free electrocatalyst. This research shows borophene derivaties fabrication and its compositional and morphological tuning for catalytic applications.

The Journal of Physical Chemistry CVol. 130(2)
Warsaw University of Technology (PL), West Pomeranian University of Technology in Szczecin (PL)
Openalex Percentile: Top 96%
Boron and Carbon Nanomaterials Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Electrocatalytic Potential of Borophene Derivatives in the Oxygen Evolution Reaction — Klaudia Maślana, Ewa Mijowska, et al. · The Journal of Physical Chemistry C (2026) | TGRS Research Map | TGRS