Abstract

A wet chemistry technique was developed to fabricate a new type of organic-inorganic hybrid solar cells with bulk p-i-n heterojunctions (“i”, an intrinsic absorber layer). Three new hyperbranched phthalocyanine polymers, namely H <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> PPc, TiOPPc and CuPPc, have been synthesized and implanted into extremely-thin absorber (ETA) solar cells with a cell structure of indium tin oxide (ITO)/TiO <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> (n-type, made by sol gel method or Solaronix method)/TiO <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> :phthalocyanine polymer/CuSCN/Au (or carbon) as the strong light-absorbing materials. The phthalocyanine polymers were prepared by cyclotetramerization reaction of 1,3-bis(3,4-dicyanophenoxy)benzene with/without respective metal salts under the catalysis of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). The phthalocyanine polymers were mixed with TiO <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> sol gel and spin-coated onto n-type TiO <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> pre-coated ITO glass substrate, followed by casting a saturated CuSCN solution in dipropylsulfide to form a p-type semiconducting layer. After coating a counter electrode onto this p-type layer, a cell structure of ITO/TiO <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> /TiO <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> :phthalocyanine polymer/CuSCN/Au (or carbon) was thus fabricated. A power conversion efficiency of 0.23% has been achieved from these devices by our preliminary work. Successful application of organic semiconductors in ETA solar cells has been demonstrated.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call