Jonas Garemark


Loading...

Last Name

Garemark

First Name

Jonas

Organisational unit

03917 - Burgert, Ingo / Burgert, Ingo

Search Results

Publications1 - 6 of 6
  • Tran, Van Chinh; Mastantuoni, Gabriella; Garemark, Jonas; et al. (2024)
    ACS Applied Materials & Interfaces
    The 3D micro- and nanostructure of wood has extensively been employed as a template for cost-effective and renewable electronic technologies. However, other electroactive components, in particular native lignin, have been overlooked due to the absence of an approach that allows access of the lignin through the cell wall. In this study, we introduce an approach that focuses on establishing conjugated-polymer-based electrical connections at various length scales within the wood structure, aiming to leverage the charge storage capacity of native lignin in wood-based energy storage electrodes. We demonstrate that poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) PEDOT/PSS, integrated within the cell wall lumen, can be interfaced with native lignin through the wood cell wall through in situ polymerization of a water-soluble S-EDOT monomer. This approach increases the capacitance of the conductive wood to 315 mF cm-2 at a scan rate of 5 mV s-1, which is seven and, respectively, two times higher compared to the capacitance of conductive wood made with the single components PEDOT/PSS or S-PEDOT. Moreover, we show that the capacitance is contributed by both the electroactive polymers and native lignin, with native lignin accounting for over 70% of the total charge storage capacity. We show that accessing native lignin through in situ creation of electrical interconnections within the wood structure offers a pathway toward sustainable, wood-based electrodes with improved charge-storage capacity for applications in electronics and energy storage.
  • Ritter, Maximilian; Maćkosz, Krzysztof; Garemark, Jonas; et al. (2025)
    ACS Nano
    The development of sustainable functional wood-based materials for advanced photonic, optical, and energy-harvesting applications is a topic of great priority and scientific interest. Owing to its inherent piezoactivity and photoconductivity, zinc oxide (ZnO) can be of help for all these applications. While previously used for wood-based piezoelectric nanogenerators, its use for enabling wood with photoconductive properties has not yet been demonstrated. Here, we introduce an innovative method to produce ZnO-wood hybrids based on atomic layer deposition (ALD), a technique so far underrepresented in the field of wood functionalization. By a studied combination of ALD, customized sample geometry, structure-retaining delignification, and careful selection of the drying method, we obtained a homogeneous functionalization of a bulk wood scaffold with layers of nanocrystalline ZnO. This approach allowed us to achieve control over the homogeneity, distribution, and coating thickness of the oxide layer. The micro- and nanostructure of the resulting hybrids were investigated by electron microscopy as well as by X-ray diffraction and scattering. The ZnO-wood hybrids show an anisotropic piezoelectric response due to the natural structure of the wood. Moreover, we demonstrate the use of ZnO-functionalized wood for the fabrication of bulk (photo)conductive wood. Upon irradiation with UV light, a significant decrease in resistivity is observed, which increases again upon removal of UV light. Finally, we used the hybrids to fabricate a ZnO-wood replica by thermal removal of the cellulose scaffold. This treatment leaves behind a detailed inorganic wood replica down to the smallest open accessible features such as micrometer-sized wood pits.
  • Garemark, Jonas; Ritter, Maximilian; Dreimol, Christopher; et al. (2025)
    Advanced Functional Materials
    The nanowatt-level power density of current biobased piezoelectric energy harvesters restricts their applicative potential for the efficient conversion of biomechanical energy. A high-performing, fully renewable piezoelectric device incorporating green piezo-active Rochelle salt in a laser-drilled wood template is demonstrated to form ordered crystal pillar arrays by melt crystallization. Investigating the effect of different crystal pillar configurations on the piezoelectric response, a shearing design (45 degrees-oriented pillars) shows potential of up to 30 V and a current of 4 mu A - corresponding to a 10-fold power increase compared to single-crystalline Rochelle salt. A concept of direct laser graphitization on the crystal surfaces are demonstrated using a fully renewable ink to create electrodes of low resistance (36 Omega sq-1). The entire device can be disassembled, fully recycled, and reused. This nanogenerator outperforms state-of-the-art biobased ones and competes with conventional lead-based devices in power generation while showing a significantly lower environmental footprint, as indicated by life-cycle assessment.
  • Dreimol, Christopher; Kürsteiner, Ronny; Ritter, Maximilian; et al. (2024)
    Small
    The transition to sustainable materials and eco-efficient processes in commercial electronics is a driving force in developing green electronics. Iron-catalyzed laser-induced graphitization (IC-LIG) has been demonstrated as a promising approach for rendering biomaterials electrically conductive. To optimize the IC-LIG process and fully exploit its potential for future green electronics, it is crucial to gain deeper insights into its catalyzation mechanism and structural evolution. However, this is challenging due to the rapid nature of the laser-induced graphitization process. Therefore, multiscale preparation techniques, including ultramicrotomy of the cross-sectional transition zone from precursor to fully graphitized IC-LIG electrode, are employed to virtually freeze the IC-LIG process in time. Complementary characterization is performed to generate a 3D model that integrates nanoscale findings within a mesoscopic framework. This enabled tracing the growth and migration behavior of catalytic iron nanoparticles and their role during the catalytic laser-graphitization process. A three-layered arrangement of the IC-LIG electrode is identified including a highly graphitized top layer with an interplanar spacing of 0.343 nm. The middle layer contained gamma-iron nanoparticles encapsulated in graphitic shells. A comparison with catalyst-free laser graphitization approaches highlights the unique opportunities that IC-LIG offers and discuss potential applications in energy storage devices, catalysts, sensors, and beyond.
  • Cortes Ruiz, Maria F.; Garemark, Jonas; Ritter, Maximilian; et al. (2024)
    Carbohydrate Polymers
    The high structural anisotropy and colloidal stability of cellulose nanofibrils' enable the creation of self-standing fibrillar hydrogel networks at very low solid contents. Adding methacrylate moieties on the surface of TEMPO oxidized CNFs allows the formation of more robust covalently crosslinked networks by free radical polymerization of acrylic monomers, exploiting the mechanical properties of these networks more efficiently. This technique yields strong and elastic networks but with an undefined network structure. In this work, we use acrylate-capped telechelic polymers derived from the step-growth polymerization of PEG diacrylate and dithiothreitol to crosslink methacrylated TEMPO-oxidized cellulose nanofibrils (MATO CNF). This combination resulted in flexible and strong hydrogels, as observed through rheological studies, compression and tensile loading. The structure and mechanical properties of these hydrogel networks were found to depend on the dimensions of the CNFs and polymer crosslinkers. The structure of the networks and the role of individual components were evaluated with SAXS (Small-Angle X-ray Scattering) and photo-rheology. A thorough understanding of hybrid CNF/polymer networks and how to best exploit the capacity of these networks enable further advancement of cellulose-based materials for applications in packaging, soft robotics, and biomedical engineering.
  • Chen, Hui; Garemark, Jonas; Li, Lengwan; et al. (2025)
    Small
    Transparent wood composites provide new functionalities through active additives distributed at the nanoscale. Scalable nanotechnology includes processing where nanoparticles and molecules are brought into the dense wood cell wall. A novel cell wall swelling step through green chemistry is therefore investigated. Sub-zero centigrade NaOH treatment provides extensive cell wall swelling. Cell wall accessibility is vastly increased so that chemicals can readily impregnate the nanostructured cell wall. Transparent wood with a thickness of up to 15 mm can therefore be fabricated. The optical transmittance and the attenuation coefficient are improved since the polymer is distributed inside the cell wall as a matrix for the nanoscale cellulose fibrils. The proposed technology paves the way for scalable wood nanoengineering.
Publications1 - 6 of 6