9 research outputs found

    Organic Farming in Bangladesh: To Pursue or not to Pursue? An Exploratory Study Based on Consumer Perception

    Get PDF
    The development of organic agriculture in Bangladesh has been slow. According to the Bangladesh Bureau of Statistics (2018), approximately 12,000 farmers in Bangladesh produce organic crops on around 7,000 hectares of land. The transition from conventional to organic farming has been an issue of debate, especially in the context of developing nations such as Bangladesh. The debate stresses the urgency for the transition to preserve environment and health and to ensure a safe, sustainable and environmentally friendly food production system, but also emphasizes the pressure of maintaining food production for a large growing population. We focus on the debate in the context of Bangladesh, and question whether it is the proper time and stage in the development process to attempt the transition from conventional to organic food production systems. We ask why the organic rice market is not expanding in Bangladesh and explain the slow market growth through the two main factors of income constraint and lack of awareness among people about the environmental and health detriments of non-organic farming. The exploratory study finds that it is not mainly the lack of awareness but the income constraint that can be principally attributed to the slow expansion of the organic rice market in Bangladesh. Through exploring consumers’ awareness about organic farming methods and their demand for organic products, this study shows how income as a major constraint, besides price, affects consumers demand for organic and non-organic rice in Bangladesh. Income being identified as the major barrier reveals the potential of the organic rice market to grow in the future, as Bangladesh continues its journey towards becoming a middle-income country

    Development and Characterization of Lead & Lead-Free Perovskite Solar Cell Materials

    Full text link
    In recent years, perovskite photovoltaic technology has offered enormous viability and dimensionality in solar cell research. As a light-harvesting active layer, Perovskite generated remarkable development in device efficiency of 25.7% for the single-junction solar cell, and over 33% for the perovskite/silicon tandem solar cell. Also, perovskite-perovskite tandem solar cell (also called all-perovskite tandem solar cell) shows great potential in device performance and achieved a power conversion efficiency (PCE) of 26.4%. Transitioning photovoltaic technology from the laboratory to commercial products, high PCE, low cost, long lifetime, and low toxicity are some of the critical factors to consider during material selection. Pb-halide perovskites have been the most studied compositions in next-generation photovoltaics due to their excellent optoelectronic properties, such as the high PCE and ideal bandgap. However, the practical relevance of these materials is hindered as they offer multifarious disadvantages, including toxicity, high water solubility and bioavailability, and thermodynamic instability. Following the toxicity and instability issues present in the Pb-based perovskites, Pb-free perovskite compounds have been the mainstay of this thesis. Several alternative cations isoelectronic to Pb, preferablyfrom groups 14 and 15, have been explored by the perovskite research community, such as Sn2+, Ge2+, Sb3+, Pt2+, Ti2+, Bi+, Ag2+, etc. In project 1, a numerical analysis of several potential Pb-free perovskite light absorber materials has been performed by modeling the device structure using the solar cell capacitance simulator, a one-dimensional (SCAPS 1D) modeling tool, and optimizing the device characteristics to theoretically determine the optimum efficiency limits for the Pb-free compounds compared to the state-of-the-art Pb-based (FA, MA, Cs)Pb(I, Br)3 perovskite. To investigate the criteria for choosing an efficient composition and key strategies to boost their performances, 4 device parameters have been optimized, such as interface band alignments, midgap defect density, the absorption coefficient, and the thickness of the perovskite absorber. Among the several alternative cations, the Sn-based perovskite absorbers are considered the best potential substitution for Pb, due to its isoelectronic configuration similar to Pb. In recent years, high-performance Sn-based HPSCs with PCE over 20% were made possible by introducing more than 50% of Sn in Pb-based perovskite, indicating a promising approach to alleviating the toxicity of lead in organic-inorganic metal halide perovskite. In project 2, an inorganic Cs(Sn,Pb)I3 perovskite with 60% Sn has been synthesized via solution processing and the effects of additive engineering on the improvement of its photovoltaic properties and stability have been investigated. The addition of the guanidinium thiocyanate (GuaSCN) additive lowers the bandgap significantly to 1.5 eV, enhances the absorption coefficient, and reduces the oxygen concentration, compared to the films with no additive. The highly oriented mixed phase of CsSnI3 and CsPbI3 has been observed in XRD, suggesting the formation of Cs(Sn, Pb)I3 perovskite. Also, it is observed that the Cs(Sn, Pb)I3 films with GuaSCN are thermally stable as they have retained the bandgap and crystal structure after being exposed to thermal annealing for 100 hours. This study suggests the addition of the GuaSCN additive is a potential route to enhance the optical properties and stability of perovskite films. The oxidation tendency of Sn2+ to Sn4+ imbalances the charge neutrality of the CsSnI3. Recently Cs2SnI6 double perovskite has emerged as a light absorber, derived from the cubic 3D structure of CsSnI3, with a higher oxidation state of Sn4+ which accounts for the intrinsic resistance to oxidation. In project 3, SnF2-doped, p-type Cs2SnI6 perovskite has been synthesized via solution processing and the influence of several solvents and additives on its photovoltaic properties and stability has been analyzed. GBL as a solvent helps in the formation of low bandgap (1.3-1.5 eV) Cs2SnI6 perovskite phase with a small amount of unreacted CsI, which has been reduced with additives. SnF2-doped crystalline Cs2SnI6 films with pyrazine and ethylene diamine (EDA) additives show significantly suppressed CsI and Cs2SnI6 preferred orientation along the (222) crystal plane and have a minority carrier lifetime of over 6 ns, which is almost twice the lifetime in films with only SnF2. This EDA-induced Cs2SnI6 perovskite film has achieved a PCE of 5.18%. Recently a Pt-based perovskite with a composition of Cs2PtI6 was developed in our previous work with a high PCE of 13.88%. However, the high cost of Pt is a hindrance to commercialization. In project 4, an experimental screening study to assess how partially replacing Pt in cesium platinum triiodide (CsPtI3) perovskite with different concentrations of earth-abundant and low-cost nickel (Ni) influences its crystallographic and optoelectronic properties has been undertaken. We report a partial substitution of PtI2 with NiCl2 in mixed PtI2-NiCl2-based films and this work will be conducted as the future work

    Additive-Assisted Optimization in Morphology and Optoelectronic Properties of Inorganic Mixed Sn-Pb Halide Perovskites

    Get PDF
    Halide perovskite solar cells (HPSCs) are promising photovoltaic materials due to their excellent optoelectronic properties, low cost, and high efficiency. Here, we demonstrate atmospheric solution processing and stability of cesium tin-lead triiodide (CsSnPbI3) thin films for solar cell applications. The effect of additives, such as pyrazine and guanidinium thiocyanate (GuaSCN), on bandgap, film morphology, structure, and stability is investigated. Our results indicate the formation of a wide bandgap (\u3e2 eV) structure with a mixed phase of tin oxide (SnO2) and Cs(Sn, Pb)I3. The addition of pyrazine decreases the intensity of SnO2 peaks, but the bandgap does not change much. With the addition of GuaSCN, the bandgap of the films reduces to 1.5 eV, and a dendritic structure of Cs(Sn, Pb)I3 is observed. GuaSCN addition also reduces the oxygen content in the films. To enable uniform film crystallization, cesium chloride (CsCl) and dimethyl sulfoxide (DMSO) additives are used in the precursor. Both CsCl and DMSO suppress dendrite formation with the latter resulting in uniform polycrystalline films with a bandgap of 1.5 eV. Heat and light soaking (HLS) stability tests at 65 degrees C and 1 sun for 100 h show all film types are stable with temperature but result in phase segregation with light exposure

    Additive-Assisted Optimization in Morphology and Optoelectronic Properties of Inorganic Mixed Sn-Pb Halide Perovskites

    No full text
    Halide perovskite solar cells (HPSCs) are promising photovoltaic materials due to their excellent optoelectronic properties, low cost, and high efficiency. Here, we demonstrate atmospheric solution processing and stability of cesium tin-lead triiodide (CsSnPbI3) thin films for solar cell applications. The effect of additives, such as pyrazine and guanidinium thiocyanate (GuaSCN), on bandgap, film morphology, structure, and stability is investigated. Our results indicate the formation of a wide bandgap (>2 eV) structure with a mixed phase of tin oxide (SnO2) and Cs(Sn, Pb)I3. The addition of pyrazine decreases the intensity of SnO2 peaks, but the bandgap does not change much. With the addition of GuaSCN, the bandgap of the films reduces to 1.5 eV, and a dendritic structure of Cs(Sn, Pb)I3 is observed. GuaSCN addition also reduces the oxygen content in the films. To enable uniform film crystallization, cesium chloride (CsCl) and dimethyl sulfoxide (DMSO) additives are used in the precursor. Both CsCl and DMSO suppress dendrite formation with the latter resulting in uniform polycrystalline films with a bandgap of 1.5 eV. Heat and light soaking (HLS) stability tests at 65 °C and 1 sun for 100 h show all film types are stable with temperature but result in phase segregation with light exposure
    corecore