REQUIMTE/LAQV, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre s/n, 4169-007 Porto, Portugal.
Instituto de Catálisis y Petroleoquímica, CSIC, C/ Marie Curie 2, Cantoblanco, 28049 Madrid, Spain.
Nanoscale. 2018 Jul 9;10(26):12820-12840. doi: 10.1039/c8nr03533d.
This work reports on the design of novel mixed valence hybrid N-doped carbon nanotubes/metal ferrite nanomaterials (MFe2O4, M(ii) = Mn, Fe, Co) with tailored composition, and magnetic and electrical properties through a straightforward eco-sustainable and less time consuming one-pot in situ coprecipitation process. The potentialities of this strategy rely on the lack of oxidative treatments to the support and thermal annealing, besides the use of aqueous conditions, a chelating base (isopropanolamine) and low temperatures. The process afforded the controlled nucleation/growth of the MFe2O4 nanoparticles (NPs), with sizes of 3.2-5.4 nm and superparamagnetic properties, on the surface of the N-doped carbon nanotubes (CNT-N) and their immobilization by covalent bonding. The nitrogen-based functionalities of CNT-N allied with the use of a coprecipitation agent with coordinating properties towards M(ii)/Fe(iii) cations were responsible for these achievements. To unravel the potentialities of the novel nanohybrids (CNT-N@M), they were tested as electrode active nanomaterials in the fabrication of all-solid-state asymmetric paper supercapacitors (SCs). All asymmetric SCs presented significantly higher performance than the symmetric CNT-N based one, with an enhancement of the energy density to up to 6.0× and of the power density to up to 4.3× due to the occurrence of both non-faradaic and faradaic charge storage mechanisms. Moreover, they led to enhanced volumetric energy density (up to 11.1×) and power density (up to 5.2×) compared with other solid-state hybrid paper SCs based on carbon materials recently reported in the literature. These results highlight the importance of conjugating a conductive support bearing N-based functionalities with MFe2O4 NPs featuring redox properties towards synergistically enhanced energy storage.
这项工作报道了通过简单、环保且耗时更短的一锅原位共沉淀法,设计具有定制组成、磁性和电学性能的新型混合价态杂化 N 掺杂碳纳米管/金属铁氧体纳米材料(MFe2O4,M(ii)=Mn、Fe、Co)。这种策略的潜力在于缺乏对载体的氧化处理和热退火,以及使用水相条件、螯合碱(异丙醇胺)和低温。该方法可以控制 MFe2O4 纳米颗粒(NPs)的成核/生长,其尺寸为 3.2-5.4nm,具有超顺磁性,且负载在 N 掺杂碳纳米管(CNT-N)的表面上,并通过共价键固定。CNT-N 的含氮官能团以及使用具有与 M(ii)/Fe(iii)阳离子配位性质的共沉淀剂是实现这些目标的原因。为了揭示新型纳米杂化物(CNT-N@M)的潜力,将其用作全固态非对称纸超级电容器(SCs)的电极活性纳米材料进行了测试。所有非对称 SCs 的性能都明显优于基于 CNT-N 的对称 SCs,由于同时存在非法拉第和法拉第电荷存储机制,能量密度提高了 6.0 倍,功率密度提高了 4.3 倍。此外,与文献中最近报道的基于碳材料的其他固态混合纸 SCs 相比,它们还具有更高的体积能量密度(提高了 11.1 倍)和功率密度(提高了 5.2 倍)。这些结果强调了将具有 N 基官能团的导电载体与具有氧化还原性能的 MFe2O4 NPs 结合起来以协同增强储能的重要性。