TY - JOUR
T1 - Electrocatalytic effects of two-dimensional (2D) layered titanate nanosheets (Ti2-x/4□x/4O4-x; □ = vacancy, x = 0.67) modified electrode for V3+/V2+ redox reactions
AU - Mutuma, Mutembei K.
AU - Park, Jeong Won
AU - Jung, Hyun
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/7/30
Y1 - 2025/7/30
N2 - Two-dimensional (2D) electrocatalysts have attracted considerable recent research interest owing to the exceptional electrical properties arising from their high anisotropy. An ideal application of 2D materials is in the catalysis of essential electrochemical reactions for energy storage. To this effect, we explored the electrocatalytic properties of exfoliated 2D layered titanate nanosheets (Ti2-x/4□x/4O4-x; □ = vacancy, x = 0.67, herein abbreviated as LTNS) for V3+/V2+ redox reaction as a model negative electrode of vanadium redox flow battery (VRFB). The dip-withdraw-dry method was used to fabricate the LTNS@CF electrode by coating pristine carbon felt (P-CF) with a very small amount (∼ 0.0043 wt% loading amount on electrode) of exfoliated LTNS colloidal aqueous suspension equivalent to cover the surface of the carbon fibers. The morphology of LTNS@CF exhibited a relatively rough surface covered by the firmly attached anisotropic LTNS compared to the smooth surface of P-CF. The electrocatalytic properties of these electrodes for V3+/V2+ redox reactions were analyzed by electrochemical impendence spectroscopy (EIS), cyclic voltammetry (CV), and VRFB single-cell, with LTNS@CF showing significantly lower charge transfer resistance (Rct) and improved kinetics for V3+/V2+ redox reaction compared to that of P-CF. This is attributed to the concurrence of desired electrocatalytic properties of the LTNS: the 2D anisotropic layered shape that facilitates charge mobility and firm attachment to the surface of carbon fibers, the negative charge of LTNS that provides electrostatic redox reaction sites for the positively charged vanadium ions, corrosion resistance of Ti-O bond in strong acidic (H2SO4) electrolyte, and its polar nature that enhances the wettability of the electrode.
AB - Two-dimensional (2D) electrocatalysts have attracted considerable recent research interest owing to the exceptional electrical properties arising from their high anisotropy. An ideal application of 2D materials is in the catalysis of essential electrochemical reactions for energy storage. To this effect, we explored the electrocatalytic properties of exfoliated 2D layered titanate nanosheets (Ti2-x/4□x/4O4-x; □ = vacancy, x = 0.67, herein abbreviated as LTNS) for V3+/V2+ redox reaction as a model negative electrode of vanadium redox flow battery (VRFB). The dip-withdraw-dry method was used to fabricate the LTNS@CF electrode by coating pristine carbon felt (P-CF) with a very small amount (∼ 0.0043 wt% loading amount on electrode) of exfoliated LTNS colloidal aqueous suspension equivalent to cover the surface of the carbon fibers. The morphology of LTNS@CF exhibited a relatively rough surface covered by the firmly attached anisotropic LTNS compared to the smooth surface of P-CF. The electrocatalytic properties of these electrodes for V3+/V2+ redox reactions were analyzed by electrochemical impendence spectroscopy (EIS), cyclic voltammetry (CV), and VRFB single-cell, with LTNS@CF showing significantly lower charge transfer resistance (Rct) and improved kinetics for V3+/V2+ redox reaction compared to that of P-CF. This is attributed to the concurrence of desired electrocatalytic properties of the LTNS: the 2D anisotropic layered shape that facilitates charge mobility and firm attachment to the surface of carbon fibers, the negative charge of LTNS that provides electrostatic redox reaction sites for the positively charged vanadium ions, corrosion resistance of Ti-O bond in strong acidic (H2SO4) electrolyte, and its polar nature that enhances the wettability of the electrode.
KW - Anisotropic two-dimensional (2D) materials
KW - Electrocatalyst
KW - Layered titanate
KW - Surface modification
KW - V/V redox reactions
UR - http://www.scopus.com/inward/record.url?scp=105001550669&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2025.163079
DO - 10.1016/j.apsusc.2025.163079
M3 - Article
AN - SCOPUS:105001550669
SN - 0169-4332
VL - 698
JO - Applied Surface Science
JF - Applied Surface Science
M1 - 163079
ER -