Loading…
Synthesis and characterization of Ti0.9Ir0.1O2-activated carbon composite as a promising support for catalysts in electrochemical energy conversion
Constructing robust support plays a key role in governing the overall catalytic efficiency of metal-based catalysts for electrochemical reactions in sustainable energy-related conversion systems. We herein use a solvothermal method to assemble Ti0.9Ir0.1O2-Activated C composites, exhibiting high sur...
Saved in:
Published in: | Advances in natural sciences. Nanoscience and nanotechnology 2023-09, Vol.14 (3), p.035003 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Constructing robust support plays a key role in governing the overall catalytic efficiency of metal-based catalysts for electrochemical reactions in sustainable energy-related conversion systems. We herein use a solvothermal method to assemble Ti0.9Ir0.1O2-Activated C composites, exhibiting high surface area and electrical conductivity compared to the pure TiO2 material. The material characterisations and electrochemical behaviours of the as-obtained composites are systemically studied by XRD, FE-SEM-EDX mapping, FT-IR, XPS, BET, four-point technique, cyclic voltammetry, etc Notably, the effect of composition on the physical and electrochemical properties of the as-made composites is also explored, which indicated the significant improvement in surface area and electrical conductivity with increasing carbon content, while a reverse trend is observed in the electrochemical durability. Among all studied composites, the Ti0.9Ir0.1O2-Activated C (50:50 wt%) composite can be a suitable support for metal-based catalysts due to its balance in physical properties (electrical conductivity of 1.5 S cm−1 and surface area of 152.12 m2 g−1) and electrochemical corrosion resistance (high durability after 2000-cycling ADT). This study can open up an efficient strategy to enhance the catalytic performance of electrochemical processes. |
---|---|
ISSN: | 2043-6254 2043-6262 |
DOI: | 10.1088/2043-6262/ace432 |