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Porosity‐Engineering of MXene as a Support Material for a Highly Efficient Electrocatalyst toward Overall Water Splitting
Author(s) -
Le Thi Anh,
Tran Ngoc Quang,
Hong Yeseul,
Kim Meeree,
Lee Hyoyoung
Publication year - 2020
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201903222
Subject(s) - electrocatalyst , mxenes , materials science , bifunctional , chemical engineering , porosity , stacking , catalysis , water splitting , electrolyte , nanotechnology , chemistry , electrode , composite material , organic chemistry , electrochemistry , photocatalysis , engineering
The use of 2 D transition metal carbide MXenes as support materials to incorporate catalytically active compounds is of interest because of their unique properties. However, the preparation of well‐dispersed catalytic phases on the inter‐connected porous MXene network is challenging and has been rarely explored. This work focuses on the synthesis of basal‐plane‐porous titanium carbide MXene (ac‐Ti 3 C 2 ) that is used subsequently as an effective host for the incorporation of a known catalytically active phase (IrCo) as an effective bifunctional electrocatalyst toward water splitting. The porous ac‐Ti 3 C 2 with abundant macro/meso/micropores is prepared by a wet chemical method at room temperature and provides ideal anchor sites for intimate chemical bonding with alien compounds. The resulting IrCo@ac‐Ti 3 C 2 electrocatalyst exhibits an excellent reactivity (220 mV at 10 mA cm −2 ) towards the oxygen evolution reaction in 1.0 m KOH, which surpasses that of the benchmark RuO 2 , a low voltage cell of 1.57 V (@ 10 mA cm −2 ) and good long‐term durability. Our work demonstrates the effectiveness of porosity engineering in MXene nanosheets as a support material to shorten ion migration pathways, to increase electrolyte accessibility between inter‐sheets and to overcome inherited re‐stacking and aggregation issues.