Supercapacitor featuring Ti3C2Tx MXene electrode: Nanoarchitectonics and electrochemical performances in aqueous and non-aqueous electrolytes

IF 5.7 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Materials Research Bulletin Pub Date : 2025-05-01 Epub Date: 2025-01-13 DOI:10.1016/j.materresbull.2025.113315
Anu M A , Merin Tomy , Manimehala U , Xavier T S
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Abstract

Ti₃C₂Tx MXenes, synthesized via HCl+LiF etching, show promise as pseudocapacitive electrodes for electrochemical energy storage, addressing the low voltage limitation of aqueous supercapacitors (SCs). This study explores Ti₃C₂Tx MXene electrodes in aqueous and gel electrolytes, specifically H₂SO₄ and H₃PO₄. Electrochemical testing, based on Dunn's approach, confirms supercapacitor-like performance, with specific capacitances of 299 F/g in 1 M aqueous H₃PO₄ and 212 F/g in H₂SO₄ at a 5 mV/s scan rate. Remarkably, in symmetric SCs with 1 M H₃PO₄, Ti₃C₂Tx MXene retains 95% capacitance at 1 V after 25,000 cycles, demonstrating excellent stability. Additionally, Ti₃C₂Tx in a 1 M gel H₃PO₄ electrolyte achieves a higher energy density of 72 Wh/kg within a 1.6 V window than with gel H₂SO₄, highlighting the impact of electrolyte choice. These findings underscore MXenes' potential as stable, high-rate electrodes for sustainable supercapacitors.

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采用Ti3C2Tx MXene电极的超级电容器:纳米结构及其在水和非水电解质中的电化学性能
Ti₃C₂Tx MXenes通过HCl+LiF刻蚀法合成,有望作为电化学储能的赝电容电极,解决了含水超级电容器(SCs)的低电压限制。这项研究探索了Ti₃C₂Tx MXene电极在水溶液和凝胶电解质中的作用,特别是H₂SO₄和H₃PO₄。基于Dunn方法的电化学测试证实了类似超级电容器的性能,在5 mV/s扫描速率下,在1 M H₃PO₄水溶液中具有299 F/g的比电容,在H₂SO₄中具有212 F/g的比电容。值得注意的是,在含有1 M H₃PO₄的对称SCs中,Ti₃C₂Tx MXene在1 V下循环25000次后保持95%的电容,表现出优异的稳定性。此外,在1 M凝胶H₃PO₄电解质中,Ti₃C₂Tx在1.6 V窗口内的能量密度比凝胶H₂SO₄更高,达到72 Wh/kg,突出了电解质选择的影响。这些发现强调了MXenes作为可持续超级电容器的稳定、高速率电极的潜力。
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来源期刊
Materials Research Bulletin
Materials Research Bulletin 工程技术-材料科学:综合
CiteScore
9.80
自引率
5.60%
发文量
372
审稿时长
42 days
期刊介绍: Materials Research Bulletin is an international journal reporting high-impact research on processing-structure-property relationships in functional materials and nanomaterials with interesting electronic, magnetic, optical, thermal, mechanical or catalytic properties. Papers purely on thermodynamics or theoretical calculations (e.g., density functional theory) do not fall within the scope of the journal unless they also demonstrate a clear link to physical properties. Topics covered include functional materials (e.g., dielectrics, pyroelectrics, piezoelectrics, ferroelectrics, relaxors, thermoelectrics, etc.); electrochemistry and solid-state ionics (e.g., photovoltaics, batteries, sensors, and fuel cells); nanomaterials, graphene, and nanocomposites; luminescence and photocatalysis; crystal-structure and defect-structure analysis; novel electronics; non-crystalline solids; flexible electronics; protein-material interactions; and polymeric ion-exchange membranes.
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