• Energy Research

Abstract Spectral conversion of the sunlight has been proposed as a method for enhancing the efficiency of photovoltaic devices, which are limited in current production by the mismatch between the solar spectrum and the wavelength range for efficient carrier generation. For example, the photo current can be increased by conversion of two low-energy photons (below the band gap of the absorber) to one higher-energy photon (i.e. upconversion). In this paper, we will review our ongoing activities aimed at enhancing such spectral-conversion processes by employing appropriately designed plasmonic nanoparticles. The nanoparticles serve as light-concentrating elements in order to enhance the non-linear upconversion process. From the theoretical side, we approach the optimization of nanoparticles by finite-element modelling of the plasmonic near fields in combination with topological optimization of the particle geometries. Experimentally, the nanostructures are formed by electron-beam lithography on thin films of Er3+-containing transparent materials, foremost TiO2 made by radio-frequency magnetron sputtering, and layers of chemically synthesized NaYF4 nanoparticles. The properties of the upconverter are measured using a variety of optical methods, including time-resolved luminescence spectroscopy on erbium transitions and spectrally resolved upconversion-yield measurements at ∼1500-nm-light excitation. The calculated near-field enhancements are validated using a technique of near-field-enhanced ablation by tunable, ultrashort laser pulses.

Abstract Spectral conversion of the sunlight has been proposed as a method for enhancing the efficiency of photovoltaic devices, which are limited in current production by the mismatch between the solar spectrum and the wavelength range for efficient carrier generation. For example, the photo current can be increased by conversion of two low-energy photons (below the band gap of the absorber) to one higher-energy photon (i.e. upconversion). In this paper, we will review our ongoing activities aimed at enhancing such spectral-conversion processes by employing appropriately designed plasmonic nanoparticles. The nanoparticles serve as light-concentrating elements in order to enhance the non-linear upconversion process. From the theoretical side, we approach the optimization of nanoparticles by finite-element modelling of the plasmonic near fields in combination with topological optimization of the particle geometries. Experimentally, the nanostructures are formed by electron-beam lithography on thin films of Er3+-containing transparent materials, foremost TiO2 made by radio-frequency magnetron sputtering, and layers of chemically synthesized NaYF4 nanoparticles. The properties of the upconverter are measured using a variety of optical methods, including time-resolved luminescence spectroscopy on erbium transitions and spectrally resolved upconversion-yield measurements at ∼1500-nm-light excitation. The calculated near-field enhancements are validated using a technique of near-field-enhanced ablation by tunable, ultrashort laser pulses.

The development of nonfullerene acceptors (NFAs) has led to dramatic improvements in the device efficiencies of organic photovoltaic (OPV) cells. To date it is, however, still unclear how those laboratory‐scale efficiencies transfer to commercial modules, and how stable these devices will be when processed via industrially compatible methods. Herein, the degradation behavior of lab‐scale and scalable OPV devices using similar nonfullerene‐based active layers is assessed. It is demonstrated that the scalable NFA OPV exhibits completely reversible degradation when assessed in ISOS‐O‐1 outdoor conditions, which is in contrast to the laboratory‐scale devices assessed via the indoor ISOS‐L‐2 protocol. Results from transient photovoltage (TPV) indicate the presence of charge trap formation, and a number of potential mechanisms are proposed for the selective occurrence of this in laboratory‐scale devices tested in ISOS‐L laboratory conditions—ultimately concluding that it has its origins in the different device architectures used. The study points at the risk of assessing active layer stability from laboratory‐scale devices and degradation studies alone and highlights the importance of using a diverse range of testing conditions and ISOS protocols for such assessment.

The development of nonfullerene acceptors (NFAs) has led to dramatic improvements in the device efficiencies of organic photovoltaic (OPV) cells. To date it is, however, still unclear how those laboratory‐scale efficiencies transfer to commercial modules, and how stable these devices will be when processed via industrially compatible methods. Herein, the degradation behavior of lab‐scale and scalable OPV devices using similar nonfullerene‐based active layers is assessed. It is demonstrated that the scalable NFA OPV exhibits completely reversible degradation when assessed in ISOS‐O‐1 outdoor conditions, which is in contrast to the laboratory‐scale devices assessed via the indoor ISOS‐L‐2 protocol. Results from transient photovoltage (TPV) indicate the presence of charge trap formation, and a number of potential mechanisms are proposed for the selective occurrence of this in laboratory‐scale devices tested in ISOS‐L laboratory conditions—ultimately concluding that it has its origins in the different device architectures used. The study points at the risk of assessing active layer stability from laboratory‐scale devices and degradation studies alone and highlights the importance of using a diverse range of testing conditions and ISOS protocols for such assessment.

Small molecule based on benzothiadiazole–triphenylamine moieties (BTD–TPA2) was designed and was employed as an effective exciton blocking layer for solar cells fabrication.

Small molecule based on benzothiadiazole–triphenylamine moieties (BTD–TPA2) was designed and was employed as an effective exciton blocking layer for solar cells fabrication.

Correction for ‘Enhancing organic solar cell lifetime through humidity control using BCF in PM6 : Y6 active layers’ by Kaike Pacheco et al., Sustainable Energy Fuels, 2024, https://doi.org/10.1039/D4SE00598H.