Stable and efficient soft perovskite crystalline film based solar cells prepared with a facile encapsulation method.

The quasi Fermi level for electrons in a soft perovskite crystalline thin film and the contact qualities at the PCBM/perovskite and perovskite/P3CT-Na interfaces can be increased using a facile encapsulation method, which improves the device performance and stability of the resultant perovskite solar cells. In the encapsulated perovskite solar cells, the averaged open-circuit voltage (VOC) largely increases from 0.981 V to 1.090 V after 9 days mainly due to the increased quasi Fermi levels. Besides, the reflectance and photoluminescence (PL) spectra show improved contact qualities at the PCBM/perovskite and perovskite/P3CT-Na interfaces, which can be used to explain the increase in the short-circuit current density (JSC) from 21.68 mA cm-2 to 23.48 mA cm-2 after the encapsulation process. Besides, nanosecond time-resolved PL and temperature-dependent PL spectra can be used to explain the increased VOC, which is mainly due to the increased shallow defect density and thereby increasing the exciton binding energy of the encapsulated perovskite sample. It is noted that the averaged power conversion efficiency (PCE) slowly decreases from 18.24% to 16.52% within 45 days.

Two-Dimensional Self-Assembly of Boric Acid-Functionalized Graphene Quantum Dots: Tunable and Superior Optical Properties for Efficient Eco-Friendly Luminescent Solar Concentrators.

Carbon-based nanomaterials hold promise for eco-friendly alternatives to heavy-metal-containing quantum dots (QDs) in optoelectronic applications. Here, boric acid-functionalized graphene quantum dots (B-GQDs) were prepared using bottom-up molecular fusion based on nitrated pyrenes and boric acid. Such B-GQDs with crystalline graphitic structures and hydrogen-bonding functionalities would be suitable model systems for unraveling the photoluminescence (PL) mechanism, while serving as versatile building blocks for supramolecular self-assembly. Unlike conventional GQDs with multiple emissive states, the B-GQDs exhibited excitation-wavelength-independent, vibronic-coupled excitonic emission. Interestingly, their PL spectra can be tuned without largely sacrificing the quantum yield (QY) due to two-dimensional self-assembly. In addition, such B-GQDs in a polystyrene matrix possessed an ultrahigh QY (∼90%) and large exciton binding energy (∼300 meV). Benefiting from broadband absorption, ultrahigh QY, and long-wavelength emission, efficient laminated luminescent solar concentrators (100 × 100 × 6.3 mm3) were fabricated, yielding a high power conversion efficiency (1.4%).

Utilizing host-guest interaction enables the simultaneous enhancement of the quantum yield and Stokes shift in organosilane-functionalized, nitrogen-containing carbon dots for laminated luminescent solar concentrators.

Solar energy can be harvested using luminescent solar concentrators (LSCs) incorporated with edge-mounted solar cells without sacrificing their see-through visibility, thus facilitating the development of solar windows. Eco-friendly carbon dots (CDs) are promising alternatives to heavy-metal-containing quantum dots in LSC applications. Unfortunately, their solid-state quantum yield (QY) at high optical density (required by laminated LSCs) is still low (<30%) and the Stokes shift is only moderate (<100 nm). Here, we studied the host-guest interaction between aminosilane-functionalized, nitrogen-containing CDs (Si-NCDs) and a silica matrix for preparing efficient laminated LSCs. We found that a sol-gel-derived silica matrix with vacuum treatment can efficiently suppress the direct nonradiative transition of the absorbing states and selectively enhance the long-wavelength-emitting surface states. Therefore, the formed Si-NCDs@silica composites simultaneously exhibited high QYs (>60%) and large Stokes shifts (>200 nm) even at a high loading content (∼10 wt%), while still exhibiting high optical transparency. Moreover, unlike conventional QY reduction upon increasing the excitation wavelengths, such high QY values can be maintained over all excitation wavelengths in the absorption region. Benefiting from these photophysical properties, efficient laminated LSCs were simply prepared, yielding a high optical efficiency of ∼4.4%.

Highly transparent and luminescent gel glass based on reabsorption-free gold nanoclusters.

Luminescent and transparent composites formed by embedding luminophores in a solid matrix are essential components for several photonic applications, such as luminescent solar concentrators (LSCs) and luminescent down-shifting/conversion layers. For these applications, the optical losses, including reabsorption and scattering need to be minimized, while the photoluminescence (PL) emission must be stable against outdoor environments. Here, highly transparent and luminescent aluminosilicate glass doped with surface-engineered gold nanoclusters (AuNCs) was prepared without involving toxic elements and hazardous solvents. Such an AuNC@glass composite with a high loading (∼14 wt%) exhibits a unique absorption profile; near-unity absorptance in the absorption range but near-zero reabsorption in the emission region, and thus generates bright PL emission with negligible reabsorption losses. Meanwhile, the PL quantum yield was enhanced (from ∼1% to ∼14%) without sacrificing the Stokes shift, while still maintaining high optical transparency. In addition, they have high stability due to the effective protection of rigid inorganic matrices, and thus would be eco-friendly candidates for further preparation of efficient and reabsorption-free LSCs.

Visible-Transparent Luminescent Solar Concentrators Based on Carbon Nanodots in the Siloxane Matrix with Ultrahigh Quantum Yields and Optical Transparency at High-Loading Contents.

Visible-transparent luminescent solar concentrators (VT-LSCs) can be integrated with solar cells for designing solar glasses. Recently, rare-earth complexes, semiconductor nanocrystals, and carbon nanodots (CNDs) have been applied in developing VT-LSCs. However, several challenges still existed, such as quantum yields (QYs) at high-loading contents, scattering/reabsorption losses, and stability. Here, highly luminescent and visible-transparent composites based on organosilane-functionalized CNDs (Si-CNDs) cross-linked in the siloxane matrix were prepared. The composites with a high-loading content (∼10 wt %) possess ultrahigh QYs of ∼94% due to surface passivation, cross-linking-enhanced emission, and negligible inter-CND energy transfer. Moreover, they still appear exceptionally transparent and, thus, are suitable for VT-LSCs. Eco-friendly VT-LSCs without colored tinting were fabricated, yielding high internal and external quantum efficiencies of ∼66% and ∼3.9%. Our demonstration would pave a bright way for the utilization of eco-friendly VT-LSCs in solar glasses.

Coordination-induced emission enhancement in gold-nanoclusters with solid-state quantum yields up to 40% for eco-friendly, low-reabsorption nano-phosphors.

Colloidal quantum dots (CQDs) have gained much attention as light-emitting materials for light-conversion nano-phosphors and luminescent solar concentrators. Unfortunately, those CQDs involve toxic heavy metals and frequently need to be synthesized in the hazardous organic solvent. In addition, they suffer from severe solid-state aggregation-induced self-quenching and reabsorption losses. To address these issues, here we prepare Zn-coordinated glutathione-stabilized gold-nanocluster (Zn-GSH-AuNCs) assemblies without involving heavy metals and organic solvent. Unlike GSH-AuNCs dispersed in an aqueous solution with poor photoluminescence quantum yields (PL-QYs, typically ~1%), those Zn-GSH-AuNCs powders hold high solid-state PL-QYs up to 40 ± 5% in the aggregated state. Such Zn-induced coordination-enhanced emission (CEE) is attributed to the combined effects of suppressed non-radiative relaxation and enhanced charge-transfer interaction. In addition, they also exhibit a large Stokes shift, thus mitigating both aggregation-induced self-quenching and reabsorption losses. Motivated by these photophysical properties, we demonstrated white-light emission from all non-toxic, aqueous-synthesis nano-materials.

Greener Luminescent Solar Concentrators with High Loading Contents Based on in Situ Cross-Linked Carbon Nanodots for Enhancing Solar Energy Harvesting and Resisting Concentration-Induced Quenching.

A luminescent solar concentrator (LSC) is composed of loaded luminophores and a waveguide that can be employed to harvest and concentrate both direct and diffused sunlight for promising applications in solar windows. Thus far, most of efficient LSCs still relied on the heavy-metal-containing colloidal quantum dots (CQDs) dispersed into a polymer matrix with a very low loading (typically <1 wt %). Such low-loading constraint is required to mitigate the concentration-induced quenching (CIQ) and maintain high optical quality and film uniformity, but this would strongly reduce the light-absorbing efficiency. To address all issues, greener LSCs with high loading concentration were prepared by in situ cross-linking organosilane-functionalized carbon nanodots (Si-CNDs), and their photophysical properties relevant to LSC operation were studied. The PL emission is stable and does not suffer from the severe CIQ effect for cross-linked Si-CNDs even with 25 wt % loadings, thus exhibiting high solid-state quantum yields (QYs) up to 45 ± 5% after the calibration of the reabsorption losses. Furthermore, such LSCs can still hold high optical quality and film uniformity, leading to low scattering losses and high internal quantum efficiency of ∼22%. However, the reabsorption losses need to be further addressed to realize large-area LSCs based on earth-abundant, cost-effective CNDs.