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TU Delft transfer-free multilayer graphene MEA (DBI2 TS4)

Source referenceSource figure
TU Delft multilayer graphene bench microelectrode array, wafer layout and 10 micrometre electrode micrograph.

Complete Figure 1: rigid fused-silica bench MEA and electrode close-up, tested on brain slices; this device is not an implant.

Scale: Original 10 µm scale bar retained in panel d. The other panels use independent scales.

In vitro brain-slice MEA on rigid fused silica; no in vivo implantation is demonstrated.

Image credit & source

Alvarez de Eulate et al., Advanced Science (2026), Figure 1 · Alvarez de Eulate et al., Advanced Science (2026), Figure 1 · CC BY 4.0.

Complete original figure extracted from the final published PDF hosted by TU Delft. No crop, resizing, annotation or image enhancement.

Source figure

TU Delft transfer-free multilayer graphene MEA (DBI2 TS4)

TU Delft multilayer graphene bench microelectrode array, wafer layout and 10 micrometre electrode micrograph.

Open full-resolution image (2050 × 1428) →

Complete Figure 1: rigid fused-silica bench MEA and electrode close-up, tested on brain slices; this device is not an implant.

Scale: Original 10 µm scale bar retained in panel d. The other panels use independent scales.

In vitro brain-slice MEA on rigid fused silica; no in vivo implantation is demonstrated.

Alvarez de Eulate et al., Advanced Science (2026), Figure 1 · Source · CC BY 4.0 · Complete original figure extracted from the final published PDF hosted by TU Delft. No crop, resizing, annotation or image enhancement.

Source referenceSource figure
Bench recording chamber and a cerebellar brain slice positioned on the graphene MEA, with recorded signals.

Complete Figure 3 shows ex vivo brain-slice placement and recording data; it does not show an implanted device.

Scale: Original panel scales retained. The recording chamber is a bench apparatus.

Ex vivo brain-slice interface; retained in the existing catalog with an explicit non-implant caveat.

Image credit & source

Alvarez de Eulate et al., Advanced Science (2026), Figure 3 · Alvarez de Eulate et al., Advanced Science (2026), Figure 3 · CC BY 4.0.

Complete original figure extracted from the final published PDF hosted by TU Delft. No crop, resizing, annotation or image enhancement.

Source figure

TU Delft transfer-free multilayer graphene MEA (DBI2 TS4)

Bench recording chamber and a cerebellar brain slice positioned on the graphene MEA, with recorded signals.

Open full-resolution image (2050 × 1259) →

Complete Figure 3 shows ex vivo brain-slice placement and recording data; it does not show an implanted device.

Scale: Original panel scales retained. The recording chamber is a bench apparatus.

Ex vivo brain-slice interface; retained in the existing catalog with an explicit non-implant caveat.

Alvarez de Eulate et al., Advanced Science (2026), Figure 3 · Source · CC BY 4.0 · Complete original figure extracted from the final published PDF hosted by TU Delft. No crop, resizing, annotation or image enhancement.

Code
L1R
Reviewed
2026-10-14
Interface
other
Evidence stage
research

Independent, source-linked catalog sheet. Not a manufacturer-issued datasheet, regulatory decision or instructions for clinical use. Human evidence does not establish approval. Source-specific restrictions, conflicts and missing specifications are retained below.

TU Delft transfer-free multilayer graphene MEA (DBI2 TS4)

A transparent microelectrode array whose recording sites are multilayer graphene grown in place on the substrate, instead of transferred from a pre-grown sheet. It is an in vitro research tool for combining electrical recording with optical imaging, tested on brain slices. It is not an implant.

Identity

FieldValue and source scope
DeviceTransfer-free multilayer graphene MEA on transparent fused silica [1]
OriginDelft University of Technology (Department of Microelectronics), with Fraunhofer IZM Berlin and Erasmus MC Rotterdam listed among author affiliations [1]
ProgrammeDutch Brain Interface Initiative, task TS4 (PI Vasiliki Giagka, TU Delft); the paper states it is part of the DBI2 project [1][3]
Radboud and Donders linkThe DBI2 annual report says graphene electrode designs were developed in collaboration with the Battaglia lab at Radboud University [3]. No Radboud or Donders author appears on the paper’s author list [1]
SpeciesMouse (acute cerebellar slices) [1]
Regulatory statusResearch device, in vitro [1]

Geometry and architecture

FieldValue and source scope
SubstrateTransparent fused silica wafer; the 4 in wafer carried 12 MEAs of different designs [1]
Array layoutThree primary designs: 60 electrodes of 10 µm in an 8 x 8 grid at 100 µm pitch; 60 electrodes of 50 µm in an 8 x 8 grid at 200 µm pitch; 32 electrodes of 30 µm in a 6 x 6 grid at 100 µm pitch. A further design spans 10 to 500 µm diameters [1]
Electrode diameters10, 30 and 50 µm tested on slices [1]
Tracks and padsInner tracks inside the imaging region are a graphene and molybdenum bilayer; outer tracks and pads are Ti/Au [1]
InsulationParylene-C, 1 to 2 µm [1]
InterfaceCustom PCB sized for Multichannel Systems 60-electrode MEA recording systems, also compatible with a TDT MZ60 interface [1]

Materials and fabrication

FieldValue and source scope
ConductorMultilayer turbostratic graphene grown by CVD on a molybdenum catalyst layer on the fused silica, so no transfer step is needed [1]
Layer countEstimated at roughly 20 to 25 layers from 47.5% transmittance at 550 nm, assuming about 2.3% absorption per layer; the authors call this a linear approximation [1]
TransparencyAbout 50% across the spectrum; 47.5% at 550 nm [1]

Performance envelope

FieldValue and source scope
Impedance5.68 ± 1.37 MΩ at 1 kHz for 10 µm electrodes (n = 42); other sizes in the paper’s supplementary table, not extracted here [1]
NoiseBaseline rms noise 2 to 7 µV [1]
Spike amplitudeUp to about 140 µV [1]
Signal to noisePublished article: 18.6 ± 2.7 dB (10 µm), 24.4 ± 6.2 dB (30 µm), 24.2 ± 4.3 dB (50 µm); abstract states up to about 25 dB. The 2025 preprint abstract states up to 30 to 40 dB [1][2]
Recording resultSpontaneous extracellular spiking from acute mouse cerebellar slices, which the authors attribute to Purkinje cells; the paper says signal quality was limited more by electrode-tissue coupling than by the MEA technology [1]
First claimedThe published abstract says it is the first demonstration that transparent graphene electrodes as small as 10 µm record extracellular spiking at these signal-to-noise ratios [1]
Annual-report statusYear 2 report: graphene MEAs with 30 µm electrodes on transparent substrates recorded spikes from brain slices; two-photon tests confirmed graphene sheet transparency [3]

Limits

In vitro slice recordings only; no implantation, animal in vivo recording or chronic data. The DBI2 task TS4 aims at flexible, stretchable, freely floating active arrays; the device here is on rigid fused silica. The paper says a flexible-substrate version of the transfer-free process was reported earlier; that version is not catalogued here. Charge injection, long-term stability and biocompatibility testing are blank.

References

  1. Alvarez de Eulate N, Pavlou C, León González G, Camarena Pérez M, Holzapfel L, Gao Z, Vollebregt S, Giagka V. Transparent transfer-free ultrasmall multilayer graphene microelectrodes enable high quality recordings in brain slices. Advanced Science 13(20):e17524 (2026), CC BY. DOI 10.1002/advs.202517524; full text PMC13067786.
  2. Preprint of the same work, bioRxiv 2025, DOI 10.1101/2025.06.13.657566, listed on the DBI2 publications page.
  3. DBI2 Annual Report, Year 2, Work Package 3, task TS4.
  4. DBI2 project page: graphene-based neural interfaces (TU Delft postdoc project, September 2023 to August 2027, owner Christos Pavlou).