Superior performance of V2O5 as hole selective contact over other transition metal oxides in silicon heterojunction solar cells

被引:135
作者
Almora, Osbel [1 ]
Gerling, Luis G. [2 ,3 ]
Voz, Cristobal [2 ]
Alcubilla, Ramon [2 ,3 ]
Puigdollers, Joaquim [2 ,3 ]
Garcia-Belmonte, Germa [1 ]
机构
[1] Univ Jaume 1, Inst Adv Mat INAM, Castellon de La Plana 12006, Spain
[2] Univ Politecn Cataluna, Dept Elect Engn, Jordi Girona 1-3, ES-08034 Barcelona, Spain
[3] Ctr Recerca Nanoengn CrNE, Pascual Vila 15, Barcelona 08028, Spain
关键词
Transition metal oxides; Silicon solar cells; Impedance spectroscopy; Passivation; Minority carrier lifetime; BACK CONTACT; RECOMBINATION;
D O I
10.1016/j.solmat.2017.04.042
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Transition metal oxides (TMOs) have recently been proved to efficiently serve as hole-selective contacts in crystalline silicon (c-Si) heterojunction solar cells. In the present work, two TMO/c-Si heterojunctions are explored using MoO3 (reference) and V2O5 as an alternative candidate. It has been found that V2O5 devices present larger (16% improvement) power conversion efficiency mainly due to their higher open-circuit voltage. While V2O5/c-Si devices with textured front surfaces exhibit larger short-circuit currents, it is also observed that flat solar cell architectures allow for passivation of the "1205/n-Si interface, giving significant carrier lifetimes of 200 mu s (equivalent to a surface recombination velocity of S-eff similar to 140 cm s(-1)) as derived from impedance analysis. As a consequence, a significant open-circuit voltage of 662 mV is achieved. It is found that, at the TMO/c-Si contact, a TMO work function enhancement Delta phi(TMO) occurs during the heterojunction formation with the consequent dipole layer enlargement Delta'=Delta+Delta phi(TMO). Our results provide new insights into the TMO/c-Si contact energetics, carrier transport across the interface and surface recombination allowing for further understanding of the nature of TMO/c-Si heterojunctions.
引用
收藏
页码:221 / 226
页数:6
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