ABSTRACT
Tin dioxide (SnO2), in perovskite solar cells (PSCs), stands out as the material most suited to the electron transport layer (ETL), yielding advantages with regard to ease of preparation, high mobility, and favorable energy level alignment. Nonetheless, there is a chance that energy losses from defects in the SnO2 and interface will result in a reduction in the Voc. Consequently, optimizing the interfaces within solar cell devices is a key to augmenting both the efficiency and the stability of PSCs. Herein this present study, we introduced butylammonium chloride (BACl) into the SnO2 ETL. The resulting optimized SnO2 film mitigated interface defect density, thereby improving charge extraction. The robust bonding capability of negatively charged Cl- ions facilitated their binding with noncoordinated Sn4+ ions, effectively passivating defects associated with oxygen vacancies and enhancing charge transport within the SnO2 ETL. Concurrently, doped BA+ and Cl- diffused into the perovskite lattice, fostering perovskite grain growth and reducing the defects in perovskite. In comparison to the control device, the Voc saw a 70 mV increase, achieving a champion efficiency of 22.86%. Additionally, following 1000 h of ambient storage, the unencapsulated device based on SnO2 preburied with BACl retained around 90% of its initial photovoltaic conversion efficiency.
ABSTRACT
Perovskite solar cell (PSC) is a promising photovoltaic technology that achieves over 26% power conversion efficiency (PCE). However, the high materials costs, complicated fabrication process, as well as poor long-term stability, are stumbling blocks for the commercialization of the PSCs in normal structures. The hole transport layer (HTL)-free carbon-based PSCs (C-PSCs) are expected to overcome these challenges. However, C-PSCs have suffered from relatively low PCE due to severe energy loss at the perovskite/carbon interface. Herein, the study proposes to boost the hole extraction capability of carbon electrode by incorporating functional manganese (II III) oxide (Mn3O4). It is found that the work function (WF) of the carbon electrode can be finely tuned with different amounts of Mn3O4 addition, thus the interfacial charge transfer efficiency can be maximized. Besides, the mechanical properties of carbon electrode can also be strengthened. Finally, a PCE of 19.03% is achieved. Moreover, the device retains 90% of its initial PCE after 2000 h of storage. This study offers a feasible strategy for fabricating efficient paintable HTL-free C-PSCs.
ABSTRACT
Capacity reduction mainly caused by the shuttle effect and low conductivity restricts the commercial application of lithium-sulfur batteries (LSBs). Herein, we developed a method to overcome these two obstacles synchronously by designing nitrogenous carbon decorated hollow Co3-xMnxO4/C nanocages as hosts of sulfur. These hosts were derived from manganese doped ZIF-67 by a facile sintering method, which provided polar surface to anchor lithium polysulfides and considerable electronic conductivity. The polar material Co3-xMnxO4 and special hollow frame contribute to efficient synergistic sulfur-fixation, resulting in great cycling stabilities. The manganese elements ensure an efficient conversion among LSPs. At the same time, N-doped carbon provides excellent electrical conductivity, thereby leading to splendid rate performances. Thus, a battery with great stability and high capacity could be achieved. As a result, Co3-xMnxO4/C/S with 66 wt% sulfur content delivered a high initial capacity of 1082 mA h g-1 at 1C, together with a slow average capacity decay of 0.056% per cycle at 10C over 500 cycles. When the average sulfur loading is 1.3 mg cm-2, a capacity of 628 mA h g-1 can be maintained at 5C after 500 cycles.
