We have tested a variety of different nanomaterials and explored their potential towards application in fast optical transceivers. This includes PbS, CuS and CdSe nanocrystals as well as Au nanoclusters. Most notably, we found that the surfaces of CdSe (
https://arxiv.org/abs/1904.04752(öffnet in neuem Fenster)) and CuS nanocrystals (
https://arxiv.org/abs/1903.05037(öffnet in neuem Fenster)) can be decorated with organic dyes to greatly expand their sensitivity for optical wavelengths which are typically not detected by these materials. In contrast, three-dimensional supercrystals of Au nanoclusters were found to exhibit highly interesting electric transport properties owing to the exceptionally large degree of long-range structural order (
https://doi.org/10.1038/s41467-020-19461-x(öffnet in neuem Fenster)) but they turned out to be chemically too unstable under intense light pulses. However, this discovery has enabled a follow-up study which utilizes this material for the cost-effective fabrication of electrical micro-circuits (
https://doi.org/10.1002/smtd.202201221(öffnet in neuem Fenster)). We have also explored the potential of Au nanorods for photodetection (
https://doi.org/10.3390/nano13091466(öffnet in neuem Fenster)). Following a similar idea, we have established a new method to print thin stripes of nanocrystal films onto electrical micro-circuits for further use as optical transceivers (
https://arxiv.org/abs/2006.11202(öffnet in neuem Fenster)). To complement the findings on optical transceivers based on nanocrystal/organic dye hybrid materials, we have detailed the interaction between these two material classes in experiment (
https://arxiv.org/abs/2005.00898(öffnet in neuem Fenster)) as well as with an extensive review of the field (
https://doi.org/10.1002/anie.201916402(öffnet in neuem Fenster)). We have designed optical transceivers based on CdSe nanocrystals and organic dyes with a 3dB bandwidth of 85 KHz (
http://arxiv.org/abs/2109.02049(öffnet in neuem Fenster)). We established that the maximum speed possible with state-of-the-art PbS nanocrystals is likely to be limited around 1 ns (
https://doi.org/10.48550/arXiv.2112.11987(öffnet in neuem Fenster)) highlighted pitfalls in accurately determining their speed (
https://doi.org/10.48550/arXiv.2209.03676(öffnet in neuem Fenster)) and we concluded our exploration of such nanocrystals coupled to organic dyes with a review of the field (
https://doi.org/10.48550/arXiv.2202.06050(öffnet in neuem Fenster)). We changed our focus material class to two-dimensional transition metal dichalocogenides and achieved a continuous development of the electrical bandwidth with such transceivers from 2.6 MHz for WSe2 (
https://doi.org/10.48550/arXiv.2203.14053(öffnet in neuem Fenster)) over 18 MHz for MoS2 (
https://doi.org/10.1039/d3na00223c(öffnet in neuem Fenster)) to >230 MHz for WSe2 (
https://doi.org/10.1039/d4lf00019f(öffnet in neuem Fenster)). We studied the electronic structure of MoS2 nanomaterials by spectroelectrochemistry (
https://doi.org/10.1002/smll.202207101(öffnet in neuem Fenster)) and monitored the effect of adsorbing organic dyes to their surface in this respect (
https://doi.org/10.26434/chemrxiv-2024-4kc0h(öffnet in neuem Fenster)) also with a special emphasis on the orientation of the molecules (
https://doi.org/10.26434/chemrxiv-2023-tj7m0(öffnet in neuem Fenster)). Combining transition metal dichalocogenides with black phosphorus enabled us to realize response times of 26 ps (
https://doi.org/10.1038/s41467-024-49760-6(öffnet in neuem Fenster)) which we recently even surpassed with a 3 ps response for combining WS2 with graphene (
https://doi.org/10.26434/chemrxiv-2024-d352b(öffnet in neuem Fenster)).