@article{6818,
  abstract     = {Indigoidine is a blue natural pigment, which can be efficiently synthetized in E. coli. In addition to its antioxidant and antimicrobial activities indigoidine due to its stability and deep blue color can find an application as an industrial, environmentally friendly dye. Moreover, similarly to its counterpart regular indigo dye, due to its molecular structure, indigoidine is an organic semiconductor. Fully conjugated aromatic moiety and intermolecular hydrogen bonding of indigoidine result in an unusually narrow bandgap for such a small molecule. This, in its turn, result is tight molecular packing in the solid state and opens a path for a wide range of application in organic and bio-electronics, such as electrochemical and field effect transistors, organic solar cells, light and bio-sensors etc.},
  author       = {Yumusak, Cigdem and Prochazkova, Anna Jancik and Apaydin, Dogukan H and Seelajaroen, Hathaichanok and Sariciftci, Niyazi Serdar and Weiter, Martin and Krajcovic, Jozef and Qin, Yong and Zhang, Wei and Zhan, Jixun and Kovalenko, Alexander},
  issn         = {0143-7208},
  journal      = {Dyes and Pigments},
  publisher    = {Elsevier},
  title        = {{Indigoidine - Biosynthesized organic semiconductor}},
  doi          = {10.1016/j.dyepig.2019.107768},
  volume       = {171},
  year         = {2019},
}

@article{6566,
  abstract     = {Methodologies that involve the use of nanoparticles as “artificial atoms” to rationally build materials in a bottom-up fashion are particularly well-suited to control the matter at the nanoscale. Colloidal synthetic routes allow for an exquisite control over such “artificial atoms” in terms of size, shape, and crystal phase as well as core and surface compositions. We present here a bottom-up approach to produce Pb–Ag–K–S–Te nanocomposites, which is a highly promising system for thermoelectric energy conversion. First, we developed a high-yield and scalable colloidal synthesis route to uniform lead sulfide (PbS) nanorods, whose tips are made of silver sulfide (Ag2S). We then took advantage of the large surface-to-volume ratio to introduce a p-type dopant (K) by replacing native organic ligands with K2Te. Upon thermal consolidation, K2Te-surface modified PbS–Ag2S nanorods yield p-type doped nanocomposites with PbTe and PbS as major phases and Ag2S and Ag2Te as embedded nanoinclusions. Thermoelectric characterization of such consolidated nanosolids showed a high thermoelectric figure-of-merit of 1 at 620 K.},
  author       = {Ibáñez, Maria and Genç, Aziz and Hasler, Roger and Liu, Yu and Dobrozhan, Oleksandr and Nazarenko, Olga and Mata, María de la and Arbiol, Jordi and Cabot, Andreu and Kovalenko, Maksym V.},
  issn         = {1936-086X},
  journal      = {ACS Nano},
  keywords     = {colloidal nanoparticles, asymmetric nanoparticles, inorganic ligands, heterostructures, catalyst assisted growth, nanocomposites, thermoelectrics},
  number       = {6},
  pages        = {6572--6580},
  publisher    = {American Chemical Society},
  title        = {{Tuning transport properties in thermoelectric nanocomposites through inorganic ligands and heterostructured building blocks}},
  doi          = {10.1021/acsnano.9b00346},
  volume       = {13},
  year         = {2019},
}

@article{6586,
  abstract     = {The bottom-up assembly of colloidal nanocrystals is a versatile methodology to produce composite nanomaterials with precisely tuned electronic properties. Beyond the synthetic control over crystal domain size, shape, crystal phase, and composition, solution-processed nanocrystals allow exquisite surface engineering. This provides additional means to modulate the nanomaterial characteristics and particularly its electronic transport properties. For instance, inorganic surface ligands can be used to tune the type and concentration of majority carriers or to modify the electronic band structure. Herein, we report the thermoelectric properties of SnTe nanocomposites obtained from the consolidation of surface-engineered SnTe nanocrystals into macroscopic pellets. A CdSe-based ligand is selected to (i) converge the light and heavy bands through partial Cd alloying and (ii) generate CdSe nanoinclusions as a secondary phase within the SnTe matrix, thereby reducing the thermal conductivity. These SnTe-CdSe nanocomposites possess thermoelectric figures of merit of up to 1.3 at 850 K, which is, to the best of our knowledge, the highest thermoelectric figure of merit reported for solution-processed SnTe.},
  author       = {Ibáñez, Maria and Hasler, Roger and Genç, Aziz and Liu, Yu and Kuster, Beatrice and Schuster, Maximilian and Dobrozhan, Oleksandr and Cadavid, Doris and Arbiol, Jordi and Cabot, Andreu and Kovalenko, Maksym V.},
  issn         = {1520-5126},
  journal      = {Journal of the American Chemical Society},
  number       = {20},
  pages        = {8025--8029},
  publisher    = {American Chemical Society},
  title        = {{Ligand-mediated band engineering in bottom-up assembled SnTe nanocomposites for thermoelectric energy conversion}},
  doi          = {10.1021/jacs.9b01394},
  volume       = {141},
  year         = {2019},
}

@article{5982,
  abstract     = {In the present work, we detail a fast and simple solution-based method to synthesize hexagonal SnSe2 nanoplates (NPLs) and their use to produce crystallographically textured SnSe2 nanomaterials. We also demonstrate that the same strategy can be used to produce orthorhombic SnSe nanostructures and nanomaterials. NPLs are grown through a screw dislocation-driven mechanism. This mechanism typically results in pyramidal structures, but we demonstrate here that the growth from multiple dislocations results in flower-like structures. Crystallographically textured SnSe2 bulk nanomaterials obtained from the hot pressing of these SnSe2 structures display highly anisotropic charge and heat transport properties and thermoelectric (TE) figures of merit limited by relatively low electrical conductivities. To improve this parameter, SnSe2 NPLs are blended here with metal nanoparticles. The electrical conductivities of the blends are significantly improved with respect to bare SnSe2 NPLs, what translates into a three-fold increase of the TE Figure of merit, reaching unprecedented ZT values up to 0.65.},
  author       = {Zhang, Yu and Liu, Yu and Lim, Khak Ho and Xing, Congcong and Li, Mengyao and Zhang, Ting and Tang, Pengyi and Arbiol, Jordi and Llorca, Jordi and Ng, Ka Ming and Ibáñez, Maria and Guardia, Pablo and Prato, Mirko and Cadavid, Doris and Cabot, Andreu},
  issn         = {1433-7851},
  journal      = {Angewandte Chemie International Edition},
  number       = {52},
  pages        = {17063--17068},
  publisher    = {Wiley},
  title        = {{Tin diselenide molecular precursor for solution-processable thermoelectric materials}},
  doi          = {10.1002/anie.201809847},
  volume       = {57},
  year         = {2018},
}