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Updated: Jan 15, 2026

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
Er-intercalated Ti3C2T x MXene electrocatalyst for efficient energy conversion
Shamaila Fatima1, Irfan Ali1, Aumber Abbas2
1Physics Characterization and Simulations Lab (PCSL), Department of Physics & Astronomy, School of Natural Sciences (SNS), National University of Sciences and Technology (NUST) Islamabad 44000 Pakistan syedrizwan@sns.nust.edu.pk syedrizwanh83@gmail.com +92 51 886 5599.
Abstract:
For sustainable green hydrogen production, bifunctional catalysts must rival or surpass precious metal electrocatalysts in water splitting. MXenes, with their rich surface chemistry, unique physicochemical properties, and stability, have emerged as promising candidates. However, achieving balanced hydrogen evolution (HER) and oxygen evolution (OER) activity in a single medium remains challenging. Herein, we report the synthesis of Ti3C2T x MXene and erbium intercalated (Er@Ti3C2T x ) nanocomposites as bifunctional electrocatalysts for overall water splitting in alkaline media. The Er@Ti3C2T x catalyst demonstrates outstanding HER performance, requiring only 256 mV overpotential at 10 mA cm-2 with a Tafel slope of 102 mV dec-1, while also exhibiting superior OER activity with an overpotential of 381 mV at 10 mA cm-2 and a Tafel slope of 157 mV dec-1. Electrochemical tests were conducted in 1 M KOH using an Ag/AgCl reference electrode and a Pt wire as the counter electrode. Chronoamperometry confirmed long-term stability and durability. Structural and morphological analyses conducted using XRD, SEM, EDX, FTIR, and Raman spectroscopy verified the successful intercalation of Er while preserving the 2D MXene structure. A notable increase in d-spacing from 8.9 Å (pristine MXene) to 12.2 Å (Er@Ti3C2T x ) further confirmed erbium (Er) incorporation. Moreover, electrochemical impedance spectroscopy (EIS) revealed reduced charge-transfer resistance, highlighting enhanced kinetics and efficiency for water-splitting reactions.
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