Pimelic dihydrazide

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CAS: 1304-39-8
MF: C7H16N4O2
MW: 188.22754
Synonyms: Pimelic dihydrazide

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Mercouri G. Kanatzidis

Northwestern University
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Gustavo E. Scuseria

Rice University
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Volker Blum

Duke University
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Co-reporter: Donghyeop Shin, Bayrammurad Saparov, Tong Zhu, William P. Huhn, Volker Blum, and David B. Mitzi
pp: 4771
Publication Date(Web):June 14, 2016
DOI: 10.1021/acs.chemmater.6b01832
Chalcogenides such as CdTe, Cu(In,Ga)(S,Se)2 (CIGSSe), and Cu2ZnSn(S,Se)4 (CZTSSe) have enabled remarkable advances in thin-film photovoltaic performance, but concerns remain regarding (i) the toxicity (CdTe) and (ii) scarcity (CIGSSe/CdTe) of the constituent elements and (iii) the unavoidable antisite disordering that limits further efficiency improvement (CZTSSe). In this work, we show that a different materials class, the BaCu2SnSexS4–x (BCTSSe) system, offers a prospective path to circumvent difficulties (i–iii) and to target new environmentally friendly and earth-abundant absorbers. Antisite disordering and associated band tailing are discouraged in BCTSSe due to the distinct coordination environment of the large Ba2+ cation. Indeed, an abrupt absorption edge and sharp associated photoluminescence emission demonstrate a reduced impact of band tailing in BCTSSe relative to CZTSSe. Our combined experimental and computational studies of BCTSSe reveal that the compositions 0 ≤ x ≤ 4 exhibit a tunable nearly direct or direct bandgap in the 1.6–2 eV range, spanning relevant values for single- or multiple-junction photovoltaic applications. For the first time, a prototype BaCu2SnS4-based thin-film solar cell has been successfully demonstrated, yielding a power conversion efficiency of 1.6% (0.42 cm2 total area). The systematic experimental and theoretical investigations, combined with proof-of-principle device results, suggest promise for BaCu2SnSexS4–x as a thin-film solar cell absorber.

David B. Mitzi

Duke University
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Co-reporter: Donghyeop Shin, Bayrammurad Saparov, Tong Zhu, William P. Huhn, Volker Blum, and David B. Mitzi
pp: 4771
Publication Date(Web):June 14, 2016
DOI: 10.1021/acs.chemmater.6b01832
Chalcogenides such as CdTe, Cu(In,Ga)(S,Se)2 (CIGSSe), and Cu2ZnSn(S,Se)4 (CZTSSe) have enabled remarkable advances in thin-film photovoltaic performance, but concerns remain regarding (i) the toxicity (CdTe) and (ii) scarcity (CIGSSe/CdTe) of the constituent elements and (iii) the unavoidable antisite disordering that limits further efficiency improvement (CZTSSe). In this work, we show that a different materials class, the BaCu2SnSexS4–x (BCTSSe) system, offers a prospective path to circumvent difficulties (i–iii) and to target new environmentally friendly and earth-abundant absorbers. Antisite disordering and associated band tailing are discouraged in BCTSSe due to the distinct coordination environment of the large Ba2+ cation. Indeed, an abrupt absorption edge and sharp associated photoluminescence emission demonstrate a reduced impact of band tailing in BCTSSe relative to CZTSSe. Our combined experimental and computational studies of BCTSSe reveal that the compositions 0 ≤ x ≤ 4 exhibit a tunable nearly direct or direct bandgap in the 1.6–2 eV range, spanning relevant values for single- or multiple-junction photovoltaic applications. For the first time, a prototype BaCu2SnS4-based thin-film solar cell has been successfully demonstrated, yielding a power conversion efficiency of 1.6% (0.42 cm2 total area). The systematic experimental and theoretical investigations, combined with proof-of-principle device results, suggest promise for BaCu2SnSexS4–x as a thin-film solar cell absorber.

Bryan Eichhorn

University of Maryland
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Xian-Bin Li

Jilin University
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Xu-Tang Tao

Shandong University
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Chuangtian Chen

Technical Institute of Physics and Chemistry
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Hong-bo Sun

Jilin University
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Li Zhao

Harbin Institute of Technology
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