Thin-Film-Engineered Self-Assembly of 3D Coaxial Microfluidics with a Tunable Polyimide Membrane for Bioelectronic Power
Pith reviewed 2026-05-16 02:33 UTC · model grok-4.3
The pith
Self-assembly rolls thin films into 3D coaxial microtubes with tunable polyimide membranes that deliver 3.1 mW cm-3 volumetric power in a 4.16 mm2 footprint.
A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.
Core claim
Strain-induced self-assembly converts patterned multilayer thin films into functional 3D coaxial Swiss-roll microtubes with total active volumes below 1 microliter, incorporating a monolithic chemically tunable polyimide proton-exchange membrane that permits post-fabrication optimization of ionic transport to balance proton conduction against mediator blocking, while a dual-mode scheme physically excludes microorganisms to reveal biofouling as the dominant failure mechanism and to maintain stable operation with excellent membrane recoverability after fouling.
What carries the argument
Strain-induced self-assembly platform that forms 3D coaxial Swiss-roll microtubes with monolithic integration of a chemically tunable polyimide proton-exchange membrane for post-assembly ionic transport optimization.
If this is right
- Biofouling is established as the primary failure mode in conventional designs rather than chemical fouling or membrane breakdown.
- Optimally treated polyimide membranes demonstrate strong recoverability after fouling events.
- Cell-free dual-mode operation maintains consistent performance by physically excluding microorganisms from the microelectronic environment.
- The thin-film approach provides a scalable route to tunable 3D bioelectronic power sources for compact autonomous microsystems.
Where Pith is reading between the lines
- The self-assembly process could be extended to incorporate additional functional layers for integrated sensing or actuation within the same small volume.
- Recovery capability of the membrane suggests potential for repeated use or longer-term operation in environments where periodic cleaning is possible.
- Arrays of these microtubes might be assembled to increase total power while retaining the ultra-compact overall footprint for distributed microscale applications.
- The physical exclusion principle could be tested in flowing biological fluids to determine if it prevents new contamination modes not seen in static tests.
Load-bearing premise
Post-fabrication chemical treatment of the polyimide membrane can reliably achieve balanced proton transport and mediator blocking while preserving mechanical integrity through the rolling process and operation.
What would settle it
Measure whether power output remains near 3.1 mW cm-3 and stability holds when live microorganisms are introduced into the same fluid compartment as the electrodes without the physical separation barrier.
read the original abstract
Thin-film self-assembly of three-dimensional (3D) microsystems presents a compelling route to integrate complex functionalities into ultra-compact volumes, yet strategies for incorporating tunable ion-conducting elements remain limited. Here, we introduce a strain-induced self assembly platform that transforms lithographically patterned multilayer thin films into functional 3D coaxial Swiss-roll microtubes with total active volumes below 1 uL. A key innovation is the monolithic integration of a chemically tunable polyimide proton-exchange membrane, enabling post-fabrication optimization of ionic transport that balances proton transport with mediator blocking. We further implement a dual-mode operational scheme that decouples microbial metabolism from electrochemical power generation, revealing biofouling, not chemical fouling or membrane degradation, as the dominant failure mechanism in conventional architectures. Critically, optimally treated polyimide membranes exhibit excellent recoverability after fouling, while cell-free mode operation maintains stable performance by physically excluding microorganisms from the microelectronic environment. This integrated bio-electronic microsystem achieves a volumetric power density of ~3.1 mW cm-3 within an ultra-compact footprint of 4.16 mm2. Our work establishes a scalable thin-film engineering approach to create tunable, 3D bioelectronic power sources for autonomous microsystems.
Editorial analysis
A structured set of objections, weighed in public.
Referee Report
Summary. The manuscript introduces a strain-induced self-assembly platform that transforms lithographically patterned multilayer thin films into 3D coaxial Swiss-roll microtubes with integrated chemically tunable polyimide proton-exchange membranes. It reports a volumetric power density of ~3.1 mW cm^{-3} in a 4.16 mm^{2} footprint, implements a dual-mode operational scheme that decouples microbial metabolism from electrochemical generation, identifies biofouling as the dominant failure mode, and claims excellent recoverability plus physical microbial exclusion in cell-free mode.
Significance. If substantiated, the work would provide a scalable thin-film route to compact bioelectronic power sources with tunable ionic transport, addressing integration challenges for autonomous microsystems and offering a potential alternative to conventional microbial fuel cell architectures limited by fouling.
major comments (3)
- [Abstract] Abstract: the reported volumetric power density of ~3.1 mW cm^{-3} is stated without error bars, replicate counts, baseline comparisons to untuned or non-coaxial controls, or quantitative membrane conductivity data, preventing verification that the value arises from the claimed membrane tuning rather than unaccounted experimental variables.
- [Results] Results section (membrane characterization): the claim that post-fabrication chemical treatment balances proton transport against mediator blocking after rolling requires before/after impedance spectra or conductivity retention metrics; without these, the attribution of stable performance to the polyimide integration cannot be assessed.
- [Discussion] Discussion (dual-mode operation): the assertion that the scheme physically excludes microorganisms lacks direct supporting evidence such as SEM, fluorescence leakage assays, or microbial ingress tests post-rolling; the reported stability could instead reflect reduced rather than excluded fouling, weakening the central architectural advantage.
minor comments (1)
- [Abstract] Abstract: the active volume is given as below 1 µL while the footprint is 4.16 mm^{2}; add a brief clarification of how the rolled coaxial geometry converts the planar footprint into the stated volumetric density for reader consistency.
Simulated Author's Rebuttal
We thank the referee for their constructive and detailed review of our manuscript. We have prepared point-by-point responses to each major comment below and will revise the manuscript to improve clarity and address the concerns where possible.
read point-by-point responses
-
Referee: [Abstract] Abstract: the reported volumetric power density of ~3.1 mW cm^{-3} is stated without error bars, replicate counts, baseline comparisons to untuned or non-coaxial controls, or quantitative membrane conductivity data, preventing verification that the value arises from the claimed membrane tuning rather than unaccounted experimental variables.
Authors: We agree that the abstract would benefit from additional statistical and comparative details to facilitate verification. The reported power density is based on experimental measurements detailed in the Results section, with baseline comparisons to untuned membranes and non-coaxial controls provided in the main text and supplementary materials. Quantitative membrane conductivity data from impedance measurements is also included in the Results. In the revised manuscript, we will update the abstract to incorporate error bars, replicate counts, and explicit references to these supporting data and comparisons. revision: yes
-
Referee: [Results] Results section (membrane characterization): the claim that post-fabrication chemical treatment balances proton transport against mediator blocking after rolling requires before/after impedance spectra or conductivity retention metrics; without these, the attribution of stable performance to the polyimide integration cannot be assessed.
Authors: The Results section discusses the impact of the post-fabrication chemical treatment on ionic transport properties. To strengthen this attribution, we will add before-and-after impedance spectra and associated conductivity retention metrics in the revised version. These additions will directly demonstrate the balance between proton transport and mediator blocking achieved through the polyimide integration. revision: yes
-
Referee: [Discussion] Discussion (dual-mode operation): the assertion that the scheme physically excludes microorganisms lacks direct supporting evidence such as SEM, fluorescence leakage assays, or microbial ingress tests post-rolling; the reported stability could instead reflect reduced rather than excluded fouling, weakening the central architectural advantage.
Authors: The dual-mode operational scheme is enabled by the coaxial rolled architecture, which is designed to physically decouple the microbial compartment from the electrode environment. The extended stability observed in cell-free mode, in contrast to rapid performance decay due to biofouling in conventional operation, provides supporting evidence for this mechanism. We will revise the Discussion to more explicitly describe the architectural basis for exclusion and include additional time-dependent performance metrics. We acknowledge that direct post-rolling imaging or ingress assays were not conducted. revision: partial
- Direct SEM, fluorescence leakage assays, or microbial ingress tests post-rolling to demonstrate physical exclusion of microorganisms.
Circularity Check
No circularity: experimental power-density claim is a direct measurement, not a derived prediction
full rationale
The manuscript describes a fabrication process (strain-induced rolling of lithographically patterned thin films) followed by post-fabrication chemical treatment of the polyimide membrane and direct experimental measurement of volumetric power density (~3.1 mW cm^{-3}). No equations, fitted parameters, or derivation chain appear in the provided text that would reduce the reported performance metric to its own inputs by construction. The central result is presented as an empirical outcome benchmarked against external units (mW cm^{-3}, mm^{2} footprint), not as a prediction obtained from a model whose parameters were tuned on the same data. Self-citations to prior thin-film self-assembly work exist but are not load-bearing for the power-density claim, which rests on physical measurements (impedance, current-voltage curves, fouling recovery) that remain independently falsifiable. Therefore the paper is self-contained against external benchmarks and receives the default non-circularity score.
Axiom & Free-Parameter Ledger
free parameters (1)
- polyimide membrane treatment conditions
axioms (1)
- domain assumption Biofouling is the dominant failure mechanism in conventional microbial fuel cell architectures
Lean theorems connected to this paper
-
IndisputableMonolith/Foundation/AlexanderDuality.leanalexander_duality_circle_linking unclear?
unclearRelation between the paper passage and the cited Recognition theorem.
strain-induced self-assembly platform that transforms lithographically patterned multilayer thin films into functional 3D coaxial Swiss-roll microtubes... monolithic integration of a chemically tunable polyimide proton-exchange membrane
-
IndisputableMonolith/Cost/FunctionalEquation.leanwashburn_uniqueness_aczel unclear?
unclearRelation between the paper passage and the cited Recognition theorem.
volumetric power density of ~3.1 mW cm^{-3} within an ultra-compact footprint of 4.16 mm^{2}
What do these tags mean?
- matches
- The paper's claim is directly supported by a theorem in the formal canon.
- supports
- The theorem supports part of the paper's argument, but the paper may add assumptions or extra steps.
- extends
- The paper goes beyond the formal theorem; the theorem is a base layer rather than the whole result.
- uses
- The paper appears to rely on the theorem as machinery.
- contradicts
- The paper's claim conflicts with a theorem or certificate in the canon.
- unclear
- Pith found a possible connection, but the passage is too broad, indirect, or ambiguous to say the theorem truly supports the claim.
Reference graph
Works this paper leans on
-
[1]
L. R. Gomez Palacios, A. G. Bracamonte, Development of nano- and microdevices for the next generation of biotechnology, wearables and miniaturized instrumentation. RSC Adv. 12(20), 12806–12822 (2022). https://doi.org/10.1039/D2RA02008D
-
[2]
A. T. Kutbee, R. R. Bahabry, K. O. Alamoudi, M. T. Ghoneim, M. D. Cordero, et al., Flexible and biocompatible high-performance solid-state micro-battery for implantable orthodontic system. npj Flex. Electron. 1(1), 7 (2017). https://doi.org/10.1038/s41528- 017-0008-7
-
[3]
J. Ni, A. Dai, Y. Yuan, L. Li, J. Lu, Three-Dimensional Microbatteries beyond Lithium Ion. Matter 2(6), 1366–1376 (2020). https://doi.org/10.1016/j.matt.2020.04.020
-
[4]
C. Santoro, F. Soavi, A. Serov, C. Arbizzani, P. Atanassov, Self-powered supercapacitive microbial fuel cell: The ultimate way of boosting and harvesting power. Biosens. Bioelectron. 78 229–235 (2016). https://doi.org/10.1016/j.bios.2015.11.026
- [5]
-
[6]
J. Ma, J. Zhang, Y. Zhang, Q. Guo, T. Hu, et al., Progress on anodic modification materials and future development directions in microbial fuel cells. J. Power Sources 556 232486 (2023). https://doi.org/10.1016/j.jpowsour.2022.232486
-
[7]
J. M. Moradian, Z. Fang, Y.-C. Yong, Recent advances on biomass-fueled microbial fuel cell. Bioresour. Bioprocess. 8(1), 14 (2021). https://doi.org/10.1186/s40643-021- 00365-7
-
[8]
Y. Cao, H. Mu, W. Liu, R. Zhang, J. Guo, et al., Electricigens in the anode of microbial fuel cells: pure cultures versus mixed communities. Microb. Cell Fact. 18(1), 39 (2019). https://doi.org/10.1186/s12934-019-1087-z
-
[9]
P. Parkhey, R. Sahu, Microfluidic microbial fuel cells: Recent advancements and future prospects. Int. J. Hydrogen Energy 46(4), 3105–3123 (2021). https://doi.org/10.1016/j.ijhydene.2020.07.019
-
[10]
B. E. Logan, M. J. Wallack, K. Y. Kim, W. He, Y. Feng, et al., Assessment of Microbial Fuel Cell Configurations and Power Densities. Environ. Sci. Technol. Lett. 2(8), 206–214 (2015). https://doi.org/10.1021/acs.estlett.5b00180
-
[11]
O. A. Ibrahim, M. Navarro-Segarra, P. Sadeghi, N. Sabaté, J. P. Esquivel, et al., Microfluidics for Electrochemical Energy Conversion. Chem. Rev. 122(7), 7236–7266 (2022). https://doi.org/10.1021/acs.chemrev.1c00499
-
[12]
L. Gong, M. Abbaszadeh Amirdehi, J. M. Sonawane, N. Jia, L. Torres de Oliveira, et al., Mainstreaming microfluidic microbial fuel cells: a biocompatible membrane grown in situ improves performance and versatility. Lab Chip 22(10), 1905–1916 (2022). https://doi.org/10.1039/D2LC00098A
-
[13]
M. A. Amirdehi, N. Khodaparastasgarabad, H. Landari, M. P. Zarabadi, A. Miled, et al., A High‐Performance Membraneless Microfluidic Microbial Fuel Cell for Stable, Long‐Term Benchtop Operation Under Strong Flow. ChemElectroChem 7(10), 2227– 2235 (2020). https://doi.org/10.1002/celc.202000040
-
[14]
W. Yang, K. K. Lee, S. Choi, A laminar-flow based microbial fuel cell array. Sensors Actuators B Chem. 243 292–297 (2017). https://doi.org/10.1016/j.snb.2016.11.155
-
[15]
Scott, Membranes and separators for microbial fuel cells
K. Scott, Membranes and separators for microbial fuel cells. in Microbial Electrochemical and Fuel Cells 153–178 (Elsevier, 2016). doi:10.1016/B978-1-78242- 375-1.00005-8. https://doi.org/10.1016/B978-1-78242-375-1.00005-8
-
[16]
F. Qian, M. Baum, Q. Gu, D. E. Morse, A 1.5 µL microbial fuel cell for on-chip bioelectricity generation. Lab Chip 9(21), 3076 (2009). https://doi.org/10.1039/b910586g
-
[17]
C. A. Machado, G. O. Brown, R. Yang, T. E. Hopkins, J. G. Pribyl, et al., Redox Flow Battery Membranes: Improving Battery Performance by Leveraging Structure–Property Relationships. ACS Energy Lett. 6(1), 158–176 (2021). https://doi.org/10.1021/acsenergylett.0c02205
-
[18]
D. Düerkop, H. Widdecke, C. Schilde, U. Kunz, A. Schmiemann, Polymer Membranes for All-Vanadium Redox Flow Batteries: A Review. Membranes (Basel). 11(3), 214 (2021). https://doi.org/10.3390/membranes11030214
-
[19]
G. L. Soloveichik, Flow Batteries: Current Status and Trends. Chem. Rev. 115(20), 11533–11558 (2015). https://doi.org/10.1021/cr500720t
-
[20]
K. B. Lam, E. F. Irwin, K. E. Healy, L. Lin, Bioelectrocatalytic self-assembled thylakoids for micro-power and sensing applications. Sensors Actuators B Chem. 117(2), 480–487 (2006). https://doi.org/10.1016/j.snb.2005.12.057
-
[21]
K. B. Lam, E. A. Johnson, M. Chiao, L. Lin, A MEMS Photosynthetic Electrochemical Cell Powered by Subcellular Plant Photosystems. J. Microelectromechanical Syst. 15(5), 1243–1250 (2006). https://doi.org/10.1109/JMEMS.2006.880296
-
[22]
M. Chiao, K. B. Lam, L. Lin, Micromachined microbial and photosynthetic fuel cells. J. Micromechanics Microengineering 16(12), 2547–2553 (2006). https://doi.org/10.1088/0960-1317/16/12/005
-
[23]
D. Karnaushenko, T. Kang, V. K. Bandari, F. Zhu, O. G. Schmidt, 3D Self-Assembled Microelectronic Devices: Concepts, Materials, Applications. Adv. Mater. 1902994 1– 30 (2019). https://doi.org/10.1002/adma.201902994
-
[24]
S. Liu, L. Wang, B. Zhang, B. Liu, J. Wang, et al., Novel sulfonated polyimide/polyvinyl alcohol blend membranes for vanadium redox flow battery applications. J. Mater. Chem. A 3(5), 2072–2081 (2015). https://doi.org/10.1039/C4TA05504G
-
[25]
X. Huang, S. Zhang, Y. Zhang, H. Zhang, X. Yang, Sulfonated polyimide/chitosan composite membranes for a vanadium redox flow battery: influence of the sulfonation degree of the sulfonated polyimide. Polym. J. 48(8), 905–918 (2016). https://doi.org/10.1038/pj.2016.42
-
[26]
J. Li, X. Yuan, S. Liu, Z. He, Z. Zhou, et al., A Low-Cost and High-Performance Sulfonated Polyimide Proton-Conductive Membrane for Vanadium Redox Flow/Static Batteries. ACS Appl. Mater. Interfaces 9(38), 32643–32651 (2017). https://doi.org/10.1021/acsami.7b07437
-
[27]
W. Xu, J. Long, J. Liu, H. Luo, H. Duan, et al., A novel porous polyimide membrane with ultrahigh chemical stability for application in vanadium redox flow battery. Chem. Eng. J. 428 131203 (2022). https://doi.org/10.1016/j.cej.2021.131203
-
[28]
D. Karnaushenko, N. Münzenrieder, D. D. Karnaushenko, B. Koch, A. K. Meyer, et al., Biomimetic Microelectronics for Regenerative Neuronal Cuff Implants. Adv. Mater. 27(43), 6797–6805 (2015). https://doi.org/10.1002/adma.201503696
-
[29]
D. D. Karnaushenko, D. Karnaushenko, D. Makarov, O. G. Schmidt, Compact helical antenna for smart implant applications. NPG Asia Mater. 7(6), e188–e188 (2015). https://doi.org/10.1038/am.2015.53
-
[30]
A. I. Egunov, Z. Dou, D. D. Karnaushenko, F. Hebenstreit, N. Kretschmann, et al., Impedimetric Microfluidic Sensor‐in‐a‐Tube for Label‐Free Immune Cell Analysis. Small 17(5), (2021). https://doi.org/10.1002/smll.202002549
-
[31]
E. Ghosh, A. I. Egunov, D. Karnaushenko, M. Medina-Sánchez, O. G. Schmidt, Self- assembled sensor-in-a-tube as a versatile tool for label-free EIS viability investigation of cervical cancer cells. Frequenz 76(11–12), 729–740 (2022). https://doi.org/10.1515/freq-2022-0090
-
[32]
S. Choi, H.-S. Lee, Y. Yang, P. Parameswaran, C. I. Torres, et al., A μL-scale micromachined microbial fuel cell having high power density. Lab Chip 11(6), 1110 (2011). https://doi.org/10.1039/c0lc00494d
-
[33]
D. Vigolo, T. T. Al-Housseiny, Y. Shen, F. O. Akinlawon, S. T. Al-Housseiny, et al., Flow dependent performance of microfluidic microbial fuel cells. Phys. Chem. Chem. Phys. 16(24), 12535 (2014). https://doi.org/10.1039/c4cp01086h
-
[34]
O. G. Schmidt, K. Eberl, Thin solid films roll up into nanotubes. Nature 410(6825), 168–168 (2001). https://doi.org/10.1038/35065525
-
[35]
V. Y. Prinz, V. Seleznev, A. . Gutakovsky, A. . Chehovskiy, V. Preobrazhenskii, et al., Free-standing and overgrown InGaAs/GaAs nanotubes, nanohelices and their arrays. Phys. E Low-dimensional Syst. Nanostructures 6(1–4), 828–831 (2000). https://doi.org/10.1016/S1386-9477(99)00249-0
-
[36]
J. Wang, D. Karnaushenko, M. Medina-Sánchez, Y. Yin, L. Ma, et al., Three- Dimensional Microtubular Devices for Lab-on-a-Chip Sensing Applications. ACS Sensors 4(6), 1476–1496 (2019). https://doi.org/10.1021/acssensors.9b00681
-
[37]
P. Lepucki, A. I. Egunov, M. Rosenkranz, R. Huber, A. Mirhajivarzaneh, et al., Self‐ Assembled Rolled‐Up Microcoils for nL Microfluidics NMR Spectroscopy. Adv. Mater. Technol. 6(1), 2000679 (2021). https://doi.org/10.1002/admt.202000679
-
[38]
Y. Lee, V. K. Bandari, Z. Li, M. Medina-Sánchez, M. F. Maitz, et al., Nano- biosupercapacitors enable autarkic sensor operation in blood. Nat. Commun. 12(1), 4– 13 (2021). https://doi.org/10.1038/s41467-021-24863-6
-
[39]
F. Gabler, D. D. Karnaushenko, D. Karnaushenko, O. G. Schmidt, Magnetic origami creates high performance micro devices. Nat. Commun. 10(1), 3013 (2019). https://doi.org/10.1038/s41467-019-10947-x
-
[40]
C. N. Saggau, F. Gabler, D. D. Karnaushenko, D. Karnaushenko, L. Ma, et al., Wafer‐ Scale High‐Quality Microtubular Devices Fabricated via Dry‐Etching for Optical and Microelectronic Applications. Adv. Mater. 32(37), 2003252 (2020). https://doi.org/10.1002/adma.202003252
-
[41]
F. Li, J. Wang, L. Liu, J. Qu, Y. Li, et al., Self-Assembled Flexible and Integratable 3D Microtubular Asymmetric Supercapacitors. Adv. Sci. 6(20), 1901051 (2019). https://doi.org/10.1002/advs.201901051
-
[42]
Z. Qu, M. Zhu, Y. Yin, Y. Huang, H. Tang, et al., A Sub-Square-Millimeter Microbattery with Milliampere-Hour-Level Footprint Capacity. Adv. Energy Mater. 12(28), 2200714 (2022). https://doi.org/10.1002/aenm.202200714
-
[43]
H. Tang, L. M. M. Ferro, D. D. Karnaushenko, O. Selyshchev, X. Wang, et al., An “Ion Harvester” Battery in Soil Empowered by a Microfluidic Pump and Interlayer Confinement within Micro‐Swiss‐Rolls. Adv. Funct. Mater. 35(14), (2025). https://doi.org/10.1002/adfm.202418872
-
[44]
M. Zhu, J. Hu, Q. Lu, H. Dong, D. D. Karnaushenko, et al., A Patternable and In Situ Formed Polymeric Zinc Blanket for a Reversible Zinc Anode in a Skin‐Mountable Microbattery. Adv. Mater. 33(8), 2007497 (2021). https://doi.org/10.1002/adma.202007497
-
[45]
D. Karnaushenko, T. Kang, O. G. Schmidt, Shapeable Material Technologies for 3D Self-Assembly of Mesoscale Electronics. Adv. Mater. Technol. 4(4), 1–29 (2019). https://doi.org/10.1002/admt.201800692
-
[46]
X. Lai, M. Yang, H. Wu, D. Li, Modular Microfluidics: Current Status and Future Prospects. Micromachines 13(8), 1–22 (2022). https://doi.org/10.3390/mi13081363
-
[47]
H. Ren, C. I. Torres, P. Parameswaran, B. E. Rittmann, J. Chae, Improved current and power density with a micro-scale microbial fuel cell due to a small characteristic length. Biosens. Bioelectron. 61 587–592 (2014). https://doi.org/10.1016/j.bios.2014.05.037
-
[48]
H. Jiang, M. A. Ali, Z. Xu, L. J. Halverson, L. Dong, Integrated Microfluidic Flow- Through Microbial Fuel Cells. Sci. Rep. 7(1), 41208 (2017). https://doi.org/10.1038/srep41208
-
[49]
J. E. Mink, J. P. Rojas, B. E. Logan, M. M. Hussain, Vertically Grown Multiwalled Carbon Nanotube Anode and Nickel Silicide Integrated High Performance Microsized (1.25 μL) Microbial Fuel Cell. Nano Lett. 12(2), 791–795 (2012). https://doi.org/10.1021/nl203801h
-
[50]
B. Şen-Doğan, M. Okan, N. Afşar-Erkal, E. Özgür, Ö. Zorlu, et al., Enhancement of the Start-Up Time for Microliter-Scale Microbial Fuel Cells (µMFCs) via the Surface Modification of Gold Electrodes. Micromachines 11(7), 703 (2020). https://doi.org/10.3390/mi11070703
-
[51]
A. Murugesan, P. Mahendran, High-Performance Polyimides with Pendant Fluorenylidene Groups: Synthesis, Characterization and Adsorption Behaviour. J. Polym. Environ. 28(9), 2393–2409 (2020). https://doi.org/10.1007/s10924-020-01777- w
-
[52]
K. A. Mauritz, R. B. Moore, State of Understanding of Nafion. Chem. Rev. 104(10), 4535–4586 (2004). https://doi.org/10.1021/cr0207123
-
[53]
A. Kusoglu, A. Z. Weber, New Insights into Perfluorinated Sulfonic-Acid Ionomers. Chem. Rev. 117(3), 987–1104 (2017). https://doi.org/10.1021/acs.chemrev.6b00159
-
[54]
S. G. A. Flimban, S. H. A. Hassan, M. M. Rahman, S.-E. Oh, The effect of Nafion membrane fouling on the power generation of a microbial fuel cell. Int. J. Hydrogen Energy 45(25), 13643–13651 (2020). https://doi.org/10.1016/j.ijhydene.2018.02.097
-
[55]
L. Zang, X.-L. Yang, H. Xu, Y.-G. Xia, H.-L. Song, A novel integrated microbial fuel cell-membrane bioreactor (MFC-MBR) for controlling the spread of antibiotic and antibiotic resistance genes while simultaneously alleviating membrane fouling. Chem. Eng. J. 487 150578 (2024). https://doi.org/10.1016/j.cej.2024.150578
-
[56]
G. Gu, X. Yang, Y. Li, J. Guo, J. Huang, et al., Advanced zwitterionic polymeric membranes for diverse applications beyond antifouling. Sep. Purif. Technol. 356 129848 (2025). https://doi.org/10.1016/j.seppur.2024.129848 Supporting materials Thin-Film-Engineered Self-Assembly of 3D Coaxial Microfluidics with a Tunable Polyimide Membrane for Bioelectronic ...
discussion (0)
Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.