Prof Henry Snaith FRS

Abstract:

We show that the use of 1,3-diaminopropane (DAP) as a chemical modifier at the perovskite/electron-transport layer (ETL) interface enhances the power conversion efficiency (PCE) of 1.7 eV band gap mixed-halide perovskite containing formamidinium and Cs single-junction cells, primarily by increasing the open-circuit voltage (VOC) from 1.06 to 1.15 V. We find that adding a postprocessing annealing step after C60 evaporation further improves device performance. Specifically, the fill factor (FF) increases by 20% in the DAP + postannealing devices compared to the control. Using hyperspectral photoluminescence microscopy, we demonstrate that annealing helps improve compositional homogeneity at the electron-transport layer (ETL) and hole-transport layer (HTL) interfaces of the solar cell, which prevents detrimental band gap pinning in the devices and improves C60 adhesion. Using time-of-flight secondary ion mass spectrometry, we show that DAP reacts with formamidinium (FA+) present at the surface of the perovskite structure to form a larger molecular cation, 1,4,5,6-tetrahydropyrimidinium (THP+), which remains at the interface. Combining the use of DAP and annealing the C60 interface, we fabricate Si-perovskite tandems with a PCE of 25.29%, compared to 23.26% for control devices. Our study underscores the critical role of the chemical reactivity of diamines at the surface and the thermal postprocessing of the C60/Lewis-base passivator interface in minimizing device losses and enhancing solar-cell performance of wide-band-gap mixed-cation mixed-halide perovskites for tandem applications.

Abstract:

Utilizing molecular bridges presents a promising means to enhance the performance of perovskite solar cells (PSCs). However, concurrently bridging the perovskite absorber and its two adjacent interfaces remains a significant challenge that is yet to be achieved. Here, we construct dual molecular bridges at perovskite heterointerfaces, enabled by a self-organizing additive of 4-fluoro-phenethylammonium formate (4-F-PEAFa) and a synthesized hole transporter of [2-(7H-dibenzo[c, g]carbazol-7-yl)ethyl]phosphonic acid (DBZ-2PACz). The molecular bridges spanning two interfaces lead to the formation of an ‘integral carrier transport pathway’, mitigating both non-radiative recombination and charge-transport losses in the fabricated PSC devices. We thus achieve a champion power conversion efficiency (PCE) of 26.0% (25.6% certified) in inverted PSCs, accompanied by an exceptionally high fill factor of 0.87 (maximum 0.88 from the certified devices, 97% of its Shockley–Queisser limit) and a low ideality factor of 1.06. The unencapsulated devices retain 96% of their PCEs after aging at 85°C for 2200 h and 90% after maximum power point tracking at an elevated temperature of 50°C for 973 h.

Abstract:

Due to minimal material use and low-cost processing, next-generation thin film solar cells represent a promising alternative to traditional crystalline silicon solar cells. Among these, metal-halide perovskite solar cells have seen significant improvements in power conversion efficiency and are now on the verge of market entry. However, most efficient and stable perovskite solar cells contain lead in the perovskite absorber layer, along with indium and silver in their electrodes. This study demonstrates an environmentally benign recycling process for recovering all three elements from end-of-life perovskite solar cells. In short, the process consists of mechanical dismantling (milling), aqueous extraction/purification of PbI2, and acid extraction and purification of indium and silver by nanofiltration. After the quantitative recovery of lead as PbI2 (95 ± 5%), indium and silver were dissolved using nitric acid with recovery rates of 87 ± 7% for both metals. Life cycle assessment calculations were used to determine optimal conditions in terms of minimal environmental impact per gram of extracted element. After acid extraction, nanofiltration was employed using both custom-made layer-by-layer membranes and commercially available acid-resistant flat sheet membranes to separate indium from silver. Using an optimized membrane design, indium was almost entirely retained (96.9 ± 0.4%) using a layer-by-layer membrane at 50% permeate recovery. Hence, a twofold concentration of indium was achieved over the course of the filtration. In contrast, silver was not retained (retention of -7.6 ± 6.3%), resulting in a dilute Ag permeate. Using the commercial flat sheet membrane resulted in similar retention rates, with 98.5 ± 0.4% for indium and 5.8 ± 11.6% for silver. However, this came at the expense of considerably higher operating pressure (25 bar vs 5 bar) and lower flux (6 L/m2h vs 30 L/m2h), resulting in higher energy demand (72 Wh/L vs 9 Wh/L). Therefore, layer-by-layer membrane filtration proved to be the superior method for element recovery from perovskite photovoltaic devices. This study has shown that combining hydrometallurgical processing (aqueous and acidic extraction) with layer-by-layer membrane filtration offers an efficient and environmentally benign approach for metal recovery from end-of-life solar cells. Since indium and silver are also key elements for other thin film photovoltaic applications, layer-by-layer membrane filtration may represent a platform technology for future photovoltaic panel recycling.