Enhancing perovskite solar cells efficiency through cesium fluoride mediated surface lead iodide modulation.

The presence of an excessive amount of lead iodide on the surface of perovskite solar cells (PSCs) is a significant contributing factor that adversely affects the stability of these devices when exposed to continuous light. To address this issue, we developed an effective strategy involving polishing PbI2 on a perovskite surface using CsF. In this study, we investigated the effects of CsF post-treatment on perovskite films and their photovoltaic properties. The results of the time-resolved photoluminescence and ultraviolet photoelectron spectroscopy tests reveal the significant positive impact of our passivation method based on CsF, which reduces the valence band offset between the perovskite and hole transport layers while simultaneously enhancing the carrier interface transport. PSCs treated with CsF exhibited a photoelectric conversion efficiency (PCE) of 24.25% and an increased fill factor (FF) of 81.72%, which surpassed those of the original PSCs (PCE = 22.12% and FF = 77.40%). Furthermore, after aging for over 2500 h at room temperature and in 30 ± 10% humidity, the PCE of the unpacked PSCs reduced to only 42% of the initial value. Furthermore, the devices treated with CsF maintained their impressive performance, with the PCE maintaining optimal levels at 91% of the initial efficiency.

Engineering NiCo2S4 nanoparticles anchored on carbon nanotubes as superior energy-storage materials for supercapacitors.

Fabricating high-capacity electrode materials toward supercapacitors has attracted increasing attention. Here we report a three-dimensional CNTs/NiCo2S4 nanocomposite material synthesized successfully by a facile one-step hydrothermal technique. As expected, a CNTs/NiCo2S4 electrode shows remarkable capacitive properties with a high specific capacitance of 890 C g-1 at 1 A g-1. It also demonstrates excellent cycle stability with an 83.5% capacitance retention rate after 5000 cycles at 10 A g-1. Importantly, when assembled into a asymmetric supercapacitor, it exhibits a high energy density (43.3 W h kg-1) and power density (800 W kg-1). The exceptional electrochemical capacity is attributed to the structural features, refined grains, and enhanced conductivity. The above results indicate that CNTs/NiCo2S4 composite electrode materials have great potential application in energy-storage devices.

Room-temperature epitaxial welding of 3D and 2D perovskites.

Formation of epitaxial heterostructures via post-growth self-assembly is important in the design and preparation of functional hybrid systems combining unique properties of the constituents. This is particularly attractive for the construction of metal halide perovskite heterostructures, since their conventional solution synthesis usually leads to non-uniformity in composition, crystal phase and dimensionality. Herein, we demonstrate that a series of two-dimensional and three-dimensional perovskites of different composition and crystal phase can form epitaxial heterostructures through a ligand-assisted welding process at room temperature. Using the CsPbBr3/PEA2PbBr4 heterostructure as a demonstration, in addition to the effective charge and energy transfer across the epitaxial interface, localized lattice strain was observed at the interface, which was extended to the top layer of the two-dimensional perovskite, leading to multiple new sub-bandgap emissions at low temperature. Given the versatility of our strategy, unlimited hybrid systems are anticipated, yielding composition-, interface- and/or orientation-dependent properties.

Promoting optoelectronic properties of Cs2AgBiBr6 nanocrystals by formation of heterostructures with BiOCl nanosheets.

Lead halide perovskite nanocrystals and their heterostructures have achieved substantial advances in optoelectronics; however, their inherent material instability and lead toxicity have driven research on alternative material systems. Herein, solution-processable heterostructures composed of lead-free double perovskite Cs2AgBiBr6 nanocrystals and BiOCl nanosheets were prepared through a colloidal synthesis method. Defect states were present in BiOCl and benefited carrier generation, recombination and transport in Cs2AgBiBr6. As a result, the light emission of the Cs2AgBiBr6 nanocrystals was greatly enhanced at low temperatures, and the photodetector based on the Cs2AgBiBr6/BiOCl heterostructure exhibited a much improved on-off ratio compared to the device based on Cs2AgBiBr6 alone. Our work highlights the complex nature and impact of two-dimensional heterostructure assembly on the optoelectronic properties of lead-free double perovskites and demonstrates their great potential toward environmentally friendly optoelectronic devices.

Preparation of Micron-sized Methylamine-PbCl3 perovskite grains by controlling phase transition engineering for selective Ultraviolet-harvesting transparent photovoltaics.

Selective ultraviolet-harvesting transparent perovskite solar cells (T-PSCs) have attracted great interest because of their high transmittance and unique photovoltaic properties, especially in the fields of smart windows for power generation and building glass. However, owing to the unsatisfactory solubility of PbCl2 in most conventional solvents, preparing transparent methylammonium lead chloride (MAPbCl3) films with high quality and sufficient thickness by conventional methods poses a substantial challenge for their application deployment in T-PSCs. In this work, two novel strategies based on an ion-exchange procedure for controlling phase transition engineering (CPTE) are proposed. For CPTE-2, an optimized cubic phase MAPbCl3 film with a large grain size and high full coverage is prepared by transforming the tetragonal phase MAPbI3 precursor into the cubic phase MAPbCl3. Establishing relevant models based on crystal parameters investigates the formation mechanism of this high-quality MAPbCl3 film. Accordingly, the resultant T-PSCs exhibit remarkable film quality and micron-sized grains and reach an optimum efficiency of 0.33% (JSC = 0.66 mA cm-2, VOC = 1.14 V, and FF = 43.72%).

Heterostructures between a tin-based intermetallic compound and a layered semiconductor for gas sensing.

SnS2 nanoplates are used as sacrificial templates to facilitate the in situ growth of intermetallic compound Pt3Sn nanoparticles. The Pt3Sn/SnS2 heterostructures show promise for selective NO2 sensing due to the favored gas adsorption and gas-solid charge transfer on Pt3Sn, combined with the optimized film conductance and formation of ohmic-type Pt3Sn/SnS2 heterointerfaces.