TY - JOUR
T1 - Cobalt Polypyridyl Complexes as Transparent Solution-Processable Solid-State Charge Transport Materials
AU - Kashif, Muhammad K.
AU - Milhuisen, Rebecca A.
AU - Nippe, Michael
AU - Hellerstedt, Jack
AU - Zee, David Z.
AU - Duffy, Noel W.
AU - Halstead, Barry
AU - De Angelis, Filippo
AU - Fantacci, Simona
AU - Fuhrer, Michael S.
AU - Chang, Christopher J.
AU - Cheng, Yi Bing
AU - Long, Jeffrey R.
AU - Spiccia, Leone
AU - Bach, Udo
N1 - Publisher Copyright:
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2016/12/21
Y1 - 2016/12/21
N2 - Charge transport materials (CTMs) are traditionally inorganic semiconductors or metals. However, over the past few decades, new classes of solution-processable CTMs have evolved alongside new concepts for fabricating electronic devices at low cost and with exceptional properties. The vast majority of these novel materials are organic compounds and the use of transition metal complexes in electronic applications remains largely unexplored. Here, a solution-processable solid-state charge transport material composed of a blend of [Co(bpyPY4)](OTf)2 and Co(bpyPY4)](OTf)3 where bpyPY4 is the hexadentate ligand 6,6′-bis(1,1-di(pyridin-2-yl)ethyl)-2,2′-bipyridine and OTf− is the trifluoromethanesulfonate anion is reported. Surprisingly, these films exhibit a negative temperature coefficient of conductivity (dσ/dT) and non-Arrhenius behavior, with respectable solid-state conductivities of 3.0 S m−1 at room temperature and 7.4 S m−1 at 4.5 K. When employed as a CTM in a solid-state dye-sensitized solar cell, these largely amorphous, transparent films afford impressive solar energy conversion efficiencies of up to 5.7%. Organic–inorganic hybrid materials with negative temperature coefficients of conductivity generally feature extended flat π-systems with strong π–π interactions or high crystallinity. The lack of these features promotes [Co(bpyPY4)](OTf)2+ x films as a new class of CTMs with a unique charge transport mechanism that remains to be explored.
AB - Charge transport materials (CTMs) are traditionally inorganic semiconductors or metals. However, over the past few decades, new classes of solution-processable CTMs have evolved alongside new concepts for fabricating electronic devices at low cost and with exceptional properties. The vast majority of these novel materials are organic compounds and the use of transition metal complexes in electronic applications remains largely unexplored. Here, a solution-processable solid-state charge transport material composed of a blend of [Co(bpyPY4)](OTf)2 and Co(bpyPY4)](OTf)3 where bpyPY4 is the hexadentate ligand 6,6′-bis(1,1-di(pyridin-2-yl)ethyl)-2,2′-bipyridine and OTf− is the trifluoromethanesulfonate anion is reported. Surprisingly, these films exhibit a negative temperature coefficient of conductivity (dσ/dT) and non-Arrhenius behavior, with respectable solid-state conductivities of 3.0 S m−1 at room temperature and 7.4 S m−1 at 4.5 K. When employed as a CTM in a solid-state dye-sensitized solar cell, these largely amorphous, transparent films afford impressive solar energy conversion efficiencies of up to 5.7%. Organic–inorganic hybrid materials with negative temperature coefficients of conductivity generally feature extended flat π-systems with strong π–π interactions or high crystallinity. The lack of these features promotes [Co(bpyPY4)](OTf)2+ x films as a new class of CTMs with a unique charge transport mechanism that remains to be explored.
KW - metallic conductivity
KW - solid-state dye-sensitized solar cells
KW - transition metal complexes
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U2 - 10.1002/aenm.201600874
DO - 10.1002/aenm.201600874
M3 - Article
AN - SCOPUS:84983782437
SN - 1614-6832
VL - 6
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 24
M1 - 1600874
ER -