Dahiru M. Sanni

This paper uses a combination of experiments and theory to study the effects of annealing temperature on the mechanical properties of hybrid organic–inorganic perovskites (HOIPs). We examined the mechanical (hardness and Young’s modulus), microstructural, and surface topography properties of the HOIP film at different annealing temperatures ranging from 80 to 170 °C. A mechanism-based strain gradient (MSG) theory is used to explain indentation size effects in films at different annealing temperatures. Intrinsic film yield strengths and hardness values (deduced from the MSG theory) are then shown to exhibit a Hall–Petch dependence on the inverse square root of the average grain size. The implications of the results are then discussed for the design of mechanically robust perovskite solar cells.

The design of electron transport layers (ETLs) with good optoelectronic properties is one of the keys to the improvement of the power conversion efficiencies (PCEs) and stability of perovskite solar cells (PSCs). Titanium dioxide (TiO₂), one of the most widely used ETL in PSCs, is characterized by low electrical conductivity that increases the series resistance of PSCs, thus limiting their PCEs. In this work, we incorporated tin oxide (SnO₂) into titanium dioxide (TiO₂) and studied the evolution of its microstructural and optoelectronic properties with SnO₂ loading. The thin films were then integrated as ETLs in a regular planar Formamidinium (FA)-rich mixed lead halide PSCs so as to assess the overall effect of SnO₂ incorporation on their charge transport and Photovoltaic (PV) characteristics. Analysis of the fabricated PSCs devices revealed that the best performing devices; based on the ETL modified with 0.2 proportion of SnO_2; had an average PCE of 17.35 ± 1.39%, which was about 7.16% higher than those with pristine TiO₂ as ETL. The improvement in the PCE of the PSC devices with 0.2 SnO₂ content in the ETL was attributed to the improved electron extraction and transport ability as revealed by the Time Resolved Photoluminescence (TRPL) and Electrochemical Impedance Spectroscopy (EIS) studies.

Incorporation of cesium (Cs) into the perovskite layer has become a good strategy to boost the stability and power conversion efficiency (PCE) of perovskite solar cells (PSCs). However, a suitable and scalable method of Cs incorporation in a perovskite film that does not cause a significant increase in the optical bandgap is needed. In this paper, we introduce a thin layer of CsBr into a formamidinium (FA)-rich mixed halide perovskite film using the thermal evaporation technique. The effects of the thickness of the CsBr layer on the microstructural, structural, and optoelectronic properties and surface chemical states of the perovskite film are then studied. The results indicate that the CsBr layer thickness is able to tune the microstructural and optoelectronic properties of the perovskite film. Planar PSCs fabricated with different thicknesses of CsBr layers in the perovskite absorber exhibited different photovoltaic performance characteristics. The CsBr-modified PSC device with a 50 nm layer of CsBr in the perovskite layer showed a better PCE of 16.19% ± 0.17%, which was about 15% higher than that of the control device, and was able to retain nearly 70% of its initial PCE value after 120 days of storage in an unencapsulated state.

This paper presents the effect of a composite poly(3,4-ethylenedioxythiophene) polystyrene sulfonate PEDOT:PSS and copper-doped nickel oxide (Cu:NiO_x) hole transport layer (HTL) on the performance of perovskite solar cells (PSCs). Thin films of Cu:NiO_x were spin-coated onto fluorine-doped tin oxide (FTO) glass substrates using a blend of nickel acetate tetrahydrate, 2-methoxyethanol and monoethanolamine (MEA) and copper acetate monohydrate. The prepared solution was stirred at 65 °C for 4 h and spin-coated onto the FTO substrates at 3000 rpm for 30 s in a nitrogen glovebox. The Cu:NiOx/FTO/glass structure was then annealed in air at 400 °C for 30 min. A mixture of PEDOT:PSS and isopropyl alcohol (IPA) (in 1:0.05 wt%) was spun onto the Cu:NiO_x/FTO/glass substrate at 4000 rpm for 60 s. The multilayer structure was annealed at 130 °C for 15 min. Subsequently, the perovskite precursor (0.95 M) of methylammonium iodide (MAI) to lead acetate trihydrate (Pb(OAc)₂·3H₂O) was spin-coated at 4000 rpm for 200 s and thermally annealed at 80 °C for 12 min. The inverted planar perovskite solar cells were then fabricated by the deposition of a photoactive layer (CH3NH3PbI3), [6,6]-phenyl C61-butyric acid methyl ester (PCBM), and a Ag electrode. The mechanical behavior of the device during the fabrication of the Cu:NiO_x HTL was modeled with finite element simulations using Abaqus/Complete Abaqus Environment CAE. The results show that incorporating Cu:NiO_x into the PSC device improves its density–voltage (J–V) behavior, giving an enhanced photoconversion efficiency (PCE) of ~12.8% from ~9.8% and ~11.5% when PEDOT:PSS-only and Cu:NiO_x-only are fabricated, respectively. The short circuit current density J_sc for the 0.1 M Cu:NiO_x and 0.2 M Cu:NiO_x-based devices increased by 18% and 9%, respectively, due to the increase in the electrical conductivity of the Cu:NiO_x which provides room for more charges to be extracted out of the absorber layer. The increases in the PCEs were due to the copper-doped nickel oxide blend with the PEDOT:PSS which enhanced the exciton density and charge transport efficiency leading to higher electrical conductivity. The results indicate that the devices with the copper-doped nickel oxide hole transport layer (HTL) are slower to degrade compared with the PEDOT:PSS-only-based HTL. The finite element analyses show that the Cu:NiO_x layer would not extensively deform the device, leading to improved stability and enhanced performance. The implications of the results are discussed for the design of low-temperature solution-processed PSCs with copper-doped nickel oxide composite HTLs.

In this research, we examined the impact of solution concentration on the photovoltaic and the material properties of perovskite solar cells (PSCs) obtained from dehydrated Pb-acetate precursors. The perovskite solution was deposited by a one-step spin-coating technique followed by 5 min of thermal annealing on a hotplate at the temperature of 90 °C to form the perovskite active layer. The PSC device structure adopted was the inverted planar architecture. The precursor solution concentrations were varied from 0.7 to 1.1M, with the optimal solution concentration found to be 1.0M. This concentration results in a power conversion efficiency of 12.2%, an open circuit voltage (Voc) of 0.94 V, a short circuit photocurrent density (Jsc) of 20.71 mA/cm2, and a fill factor of 62.69%. Our investigations revealed that the precursor solution concentration had a huge effect on the quality of the perovskite film and the photovoltaic properties of the PSCs.

This paper presents the results of pressure-effects on performance characteristics of near-infra-red perovskite light emitting diodes (PeLEDs) using a combination of experimental and analytical/computational approaches. First, pressure-effects are studied using models that consider the deformation and contacts that occur around interfacial impurities and interlayer surface roughness in PeLEDs. The predictions from the model show that the sizes of the interfacial defects decrease with increasing applied pressure. The current–voltage characteristics of the fabricated devices are also presented. These show that the PeLEDs have reduced turn-on voltages (from 2.5 V to 1.5 V) with the application of pressure. The associated pressure-induced reductions in the defect density and the bandgaps of the perovskite layer are then used to explain the improved performance characteristics of the PeLED devices.

In this research, we demonstrated the use of hafnium acetylacetonate (Hfaca) dissolved in ethanol as a buffer layer for perovskite solar cells from non-halide Pb (dehydrated lead acetate) source material. The inverted p-i-n planar heterojunction structure was employed in this work. A one step spin-coating method was used in depositing the perovskite solution before thermal annealing at 90 °C for 5 min to form the perovskite film. Hfaca has been previously used as a buffer layer, but the optimal concentration has not been reported. The optimum concentration of Hfaca was found to be 1.0 mg/ml, resulting in a power conversion efficiency (PCE) of 12.23% corresponding to more than 30% improvement when compared to the control device (phenyl-C₆₁-butyric acid methyl ester/Ag) without Hfaca, which has a PCE of 8.89%. Hfaca as a buffer layer leads to superior stability, retaining about 90% of its original PCE values after 15 days of storage in a glove box, compared to the control device, which retains 70% of the initial PCE value under the same storage.

Following the increasing global awareness of the dangers posed by the present state of climate change, many countries such as Uganda have adapted long-term plans for a transition to decarbonised economies. A major strategy for decarbonisation is to replace fossil fuels with renewable energy (RE) sources as the fundamental energy source. Uganda has substantial RE resources for the provision of energy services and production, yet these resources remain untapped. It is therefore crucial that the use of these abundant resources should be heightened. This paper examines and discusses the potential and current RE utilization and development in Uganda from the perspective of sustainable development. The status of the different RE resources and their application/utilization, including details of existing projects in the country, are carefully explored and discussed. The possible drivers for a huge advancement of RE applications and development in Uganda are also discussed before elucidating the major barriers and challenges faced by the energy sector as regards RE. Measures and policies required to facilitate the utilization of RE in Uganda are proposed. These evidence-based policies could guide the delivery of affordable and sustainable energy solutions for all by 2030 in Uganda.