摘要
Transition metal oxides (TMOs) with high work function (WF) are typically used for hole selective layers for crystalline silicon (c-Si) heterojunction solar cells. Among them, tungsten oxide (WO3−x) exhibits a wide bandgap and high thermal stability; however, the photoelectrical conversion efficiency (PCE) of solar cells based on WO3−x lags behind its counterparts (MoO3−x and V2O5−x). Moreover, the films are usually deposited by vacuum methods, which makes it difficult to modulate the WF or oxygen vacancies (VO) to improve the hole selectivity. In this work, a low cost, solution-processed WO3−x film with ion doping is deposited as a hole selective layer for p-Si heterojunction solar cells. Experimental results and density functional theory calculations demonstrate that Ta5+ tends to replace W5+ and strengthens the W–O binding, which facilitate the reduction of VO and increase the WF of WO3−x films, resulting in the increase of band bending of the c-Si surface and the improvement of hole selectivity. The solar cells with a structure of p-Si/Ta5+:WO3−x/Ag have achieved a remarkable PCE of 18.67%, which is the highest efficiency obtained for WO3−x/c-Si heterojunctions based on solution processing up to now. This work also paves the way for extending the doping strategy of WO3−x to other optoelectronic device applications.
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