Harrison Ka Hin Lee

Is organic photovoltaics promising for indoor applications

This work utilizes organic photovoltaics (OPV) for indoor applications, such as powering small electronic devices or wireless connected Internet of Things. Three representative polymer-based OPV systems, namely, poly(3-hexylthiophene-2,5-diyl), poly[N-9′-heptadecanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)], and poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl][3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl]], were selected as the donor materials in blend with fullerene derivatives for comparison under low light level condition using fluorescent lamps. PCDTBT based devices are found to be the best performing system, generating 13.9 μW/cm2 corresponding to 16.6% power conversion efficiency at 300 lx, although PTB7 based devices show the highest efficiency under one sun conditions. This high performance suggests that OPV is competitive to the other PV technologies under low light condition despite much lower performance under one sun conditi...

Organic photovoltaic cells – promising indoor light harvesters for self-sustainable electronics

Photovoltaic cells are attracting significant interest for harvesting indoor light for low power consumption wireless electronics such as those required for smart homes and offices, and the rapidly-growing Internet of Things. Here, we explore the potential of solution processable, small molecule photovoltaic cells as indoor power sources. By optimizing the solvent vapour annealing (SVA) time for the photovoltaic layer, a balance between its crystallization and phase separation is obtained, resulting in a record power conversion efficiency (PCE) of over 28% under fluorescent lamps of 1000 lux, generating a maximum power density of 78.2 μW cm−2 (>10% PCE under AM1.5G). This high indoor performance surpasses that of silicon based photovoltaic cells, and is similar to that of gallium arsenide photovoltaic cells. Besides, the ratios of the voltage at the maximum power point (MPP) to the open circuit voltage are similar from indoor lighting to one sun conditions, which is unique and allows a less power consuming method to track the MPP for a broad range of light intensities (potentially attractive for wearable photovoltaics). New insight into the effect of SVA on the indoor and one sun performance is provided using advanced optoelectronic characterization techniques, which show that the mobility-lifetime products as a function of charge carrier density can be correlated well with the performance at different light levels. Our results suggest that organic photovoltaic cells could be promising as indoor power sources for self-sustainable electronics.

The role of fullerenes in the environmental stability of polymer:fullerene solar cells

Environmental stability is a common challenge for the commercialisation of low cost, encapsulation-free organic opto-electronic devices. Understanding the role of materials degradation is the key to address this challenge, but most such studies have been limited to conjugated polymers. Here we quantitatively study the role of the common fullerene derivative PCBM in limiting the stability of benchmark organic solar cells, showing that a minor fraction (<1%) of photo-oxidised PCBM, induced by short exposure to either solar or ambient laboratory lighting conditions in air, consistent with typical processing and operating conditions, is sufficient to compromise device performance severely. We identify the effects of photo-oxidation of PCBM on its chemical structure, and connect this to specific changes in its electronic structure, which significantly alter the electron transport and recombination kinetics. The effect of photo-oxidation on device current–voltage characteristics, electron mobility and density of states could all be explained with the same model of photoinduced defects acting as trap states. Our results demonstrate that the photochemical instability of PCBM and chemically similar fullerenes remains a barrier for the commercialisation of organic opto-electronic devices.

Impact of Aggregation on the Photochemistry of Fullerene Films: Correlating Stability to Triplet Exciton Kinetics

The photochemistry and stability of fullerene films is found to be strongly dependent upon film nanomorphology. In particular, PC61BM blend films, dispersed with polystyrene, are found to be more susceptible to photobleaching in air than the more aggregated neat films. This enhanced photobleaching correlated with increased oxygen quenching of PC61BM triplet states and the appearance of a carbonyl FTIR absorption band indicative of fullerene oxidation, suggesting PC61BM photo-oxidation is primarily due to triplet-mediated singlet oxygen generation. PC61BM films were observed to undergo photo-oxidation in air for even modest (≤40 min) irradiation times, degrading electron mobility substantially, indicative of electron trap formation. This conclusion is supported by observation of red shifts in photo- and electro-luminescence with photo-oxidation, shown to be in agreement with time-dependent density functional theory calculations of defect generation. These results provide important implications on the environmental stability of PC61BM-based films and devices.

Dark electrical bias effects on moisture-induced degradation in inverted lead halide perovskite solar cells measured by using advanced chemical probes

Emerging lead halide perovskite materials have enormous potential for application in a range of optoelectronic devices, such as solar cells, light emitting diodes, transistors and lasers. However, the large-scale commercialization of these technologies will depend on the ability of the active material to be stable under environmental and operating conditions. In this work, we measured for the first time the electrical bias-induced degradation of inverted perovskite solar cells in the dark in different environments and concluded that humidity coupled with electrical bias results in fast degradation of CH3NH3PbI3 into PbI2. Micro-Raman and photoluminescence show that the degradation starts from the edge of the cell due to moisture ingress. By using novel local Raman-transient photocurrent measurements, we were able to probe local ion migration in the degraded region and non-degraded region and found that the formation of PbI2 can passivate the perovskite by reducing ion migration. The degradation is far from uniform across different grains as revealed by secondary electron hyperspectral imaging, an advanced scanning electron microscopy technique which allows probing the composition of individual grains from the cross section. By using potential step chronoamperometry, we also found that the bias degradation is closely related to the density of mobile ions. The unique combination of established methods with several novel analytical tools provides an insight into the origin of the bias-degradation of inverted perovskite solar cells from the nano-scale to the cell level, and demonstrates the potential of these novel tools for studying the degradation in other perovskite systems.

Photo-stability study of a solution-processed small molecule solar cell system: correlation between molecular conformation and degradation

Abstract Solution-processed organic small molecule solar cells (SMSCs) have achieved efficiency over 11%. However, very few studies have focused on their stability under illumination and the origin of the degradation during the so-called burn-in period. Here, we studied the burn-in period of a solution-processed SMSC using benzodithiophene terthiophene rhodamine:[6,6]-phenyl C71 butyric acid methyl ester (BTR:PC71BM) with increasing solvent vapour annealing time applied to the active layer, controlling the crystallisation of the BTR phase. We find that the burn-in behaviour is strongly correlated to the crystallinity of BTR. To look at the possible degradation mechanisms, we studied the fresh and photo-aged blend films with grazing incidence X-ray diffraction, UV–vis absorbance, Raman spectroscopy and photoluminescence (PL) spectroscopy. Although the crystallinity of BTR affects the performance drop during the burn-in period, the degradation is found not to originate from the crystallinity changes of the BTR phase, but correlates with changes in molecular conformation – rotation of the thiophene side chains, as resolved by Raman spectroscopy which could be correlated to slight photobleaching and changes in PL spectra.