Rational design of NiMoO4/carbon nanocomposites for high-performance supercapacitors: an in situ carbon incorporation approach†

IF 3.2 Q2 CHEMISTRY, PHYSICAL Energy advances Pub Date : 2024-11-08 DOI:10.1039/D4YA00438H
Raji Yuvaraja, Sankar Sarathkumar, Venkatesan Gowsalya, Sorna Pandian Anitha Juliet, Selvakumar Veeralakshmi, Siva Kalaiselvam, Gunniya Hariyanandam Gunasekar and Selvan Nehru
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Abstract

Understanding the impact of different compositions of nanocomposites synthesized via in situ incorporation of different ratios of carbon with metal oxides is an important factor for designing efficient electrode materials for high-performance supercapacitors. Here, a series of nanomaterials, NiMoO4, carbonaceous nanospheres (CNSs), and NiMoO4/C nanocomposites (NiMoO4/C (Dx), where, x = 10, 25, 50, and 75 represents the molar ratio of dextrose (D) to Ni2+), have been synthesized via an in situ hydrothermal method. The structural and surface analysis revealed the efficient integration of NiMoO4 and carbon in the NiMoO4/C (D50) nanocomposite, consisting of 71.1% NiMoO4 and 28.9% carbon components. The nanocomposite features a graphitic carbon sheet-like structure embedded with NiMoO4 nanorods, showing increased defects with higher carbon content and enhanced surface area with larger mesoporosity. In three-electrode supercapacitor studies for these electrode materials using 3 M KOH as the electrolyte, the NiMoO4/C (D50)-based electrode delivered superior specific capacitance (940 F g−1) at a current density of 1 A g−1 compared to bare NiMoO4 (520 F g−1), CNS (75 F g−1) and NiMoO4/C (D10, D25 and D75) nanocomposites (436–583 F g−1), with 71% capacity retention up to 5000 cycles. Furthermore, for the fabricated NiMoO4/C (D50)-based two-electrode supercapacitors at 1 A g−1 using 3 M KOH, the symmetric configuration delivered a doubled specific capacitance (83 F g−1), while the asymmetric configuration led to a doubled performance in both energy density (14.2 W h kg−1) and power density (444 W kg−1), in comparison to each other. The enhanced supercapacitor performance of NiMoO4/C (D50) can be attributed to the synergistic effect between carbon and NiMoO4 in the optimized nanocomposites, which improves the electrolyte-philicity by altering the surface composition and properties, leading to more electroactive sites and increased charge storage capacity. Thus, designing new electrode materials via in situ hydrothermal synthesis of different metal oxide/C nanocomposites with optimal composition and choosing different carbon source materials will deliver high-performance supercapacitors in the near future.

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高性能超级电容器用NiMoO4/碳纳米复合材料的合理设计:原位碳掺入方法
了解不同碳与金属氧化物的原位掺入比例对纳米复合材料的影响是设计高性能超级电容器电极材料的重要因素。本文采用原位水热法合成了一系列纳米材料NiMoO4、碳质纳米球(CNSs)和NiMoO4/C纳米复合材料(NiMoO4/C (Dx),其中x = 10、25、50和75分别代表葡萄糖(D)与Ni2+的摩尔比)。结构和表面分析表明,NiMoO4/C (D50)纳米复合材料的NiMoO4组分和碳组分分别为71.1%和28.9%,实现了NiMoO4和碳的有效结合。纳米复合材料具有嵌入NiMoO4纳米棒的石墨碳片状结构,碳含量越高,缺陷越多,介孔越大,表面积越大。在使用3 M KOH作为电解液的三电极超级电容器研究中,与NiMoO4 (520 F g−1),CNS (75 F g−1)和NiMoO4/C (D10, D25和D75)纳米复合材料(436-583 F g−1)相比,NiMoO4/C (D10, D25和D75)电极材料在电流密度为1 a g−1的情况下具有优异的比电容(940 F g−1),高达5000次循环的容量保持率为71%。此外,对于制备的NiMoO4/C (D50)双电极超级电容器,在1 A g−1下,使用3 M KOH,对称结构提供了两倍的比电容(83 F g−1),而非对称结构在能量密度(14.2 W h kg−1)和功率密度(444 W kg−1)方面的性能都是两倍的。NiMoO4/C (D50)超级电容器性能的增强可归因于优化后的纳米复合材料中碳与NiMoO4之间的协同作用,通过改变表面组成和性能来提高电解质亲水性,从而产生更多的电活性位点和更高的电荷存储容量。因此,通过原位水热合成不同的金属氧化物/碳纳米复合材料并选择不同的碳源材料来设计新的电极材料将在不久的将来提供高性能的超级电容器。
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