Cs and Br tuning to achieve ultralow-hysteresis and high-performance indoor triple cation perovskite solar cell with low-cost carbon-based electrode.

With high efficacy for electron-photon conversion under low light, perovskite materials show great potential for indoor solar cell applications to power small electronics for internet of things (IoTs). To match the spectrum of an indoor LED light source, triple cation perovskite composition was varied to adjust band gap values via Cs and Br tuning. However, increased band gaps lead to morphology, phase instability, and defect issues. 10% Cs and 30% Br strike the right balance, leading to low-cost carbon-based devices with the highest power conversion efficiency (PCE) of 31.94% and good stability under low light cycles. With further improvement in device stack and size, functional solar cells with the ultralow hysteresis index (HI) of 0.1 and the highest PCE of 30.09% with an active area of 1 cm2 can be achieved. A module from connecting two such cells in series can simultaneously power humidity and temperature sensors under 1000 lux.

Unraveling the Adsorption Behavior of Thymol on Carbon and Silica Nanospheres for Prolonged Antibacterial Activity: Experimental and DFT Studies.

Functionalization of thymol (Thy) on nanocarriers is a key step in achieving prolonged antimicrobial activity. This requires nanomaterials with uniform particle diameters and suitable thymol sorption. Herein, hollow carbon (HC) and SiO2-carbon core-shell (SiO2@C) were investigated due to their diverse morphologies and ease of surface modification. HC (14 ± 1 nm size) and SiO2@C (10 ± 1.5 nm size) were synthesized by the Stöber method before thymol was loaded by incipient wetness impregnation. Nanoparticle physicochemical properties were characterized by advanced techniques, including X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS). Adsorption energies of thymol on the carbon and SiO2 surfaces were elucidated by density functional theory (DFT) simulations. Moreover, the in vitro thymol release profiles and antibacterial activity were evaluated. The experimental results indicated that the oxy-carbon surface species of HC led to longer thymol release profiles than the -OH group of SiO2@C. The DFT calculations revealed that the weaker physical interaction of thymol on HC was better for drug release than that on SiO2@C. Thus, a longer thymol release profile of HC with hollow structures showed better antibacterial performance against Gram-positive bacteria Staphylococcus aureus than that of SiO2@C with core-shell structures. This work confirms the important role of carbon morphology and specific functional groups in thymol release profiles for the further development of inhibition products.

Improving morphology and optoelectronic properties of ultra-wide bandgap perovskite via Cs tuning for clear solar cell and UV detection applications.

With growing population, vertical spaces from skyscrapers are vast. Semi-transparent solar cells enable an effective pathway for vertical energy harvesting. With composition tunability, perovskite materials can be designed with different transparencies and colors. In this work, an ultra-high bandgap layered triple cation perovskite system was developed for the first time to meet the demand of clear optoelectronic applications; low dimensional triple cation perovskite thin films were fabricated using perovskite with the formula (PEA)2(CsxMA0.61-xFA0.39)39(Pb)40(Cl0.88-0.32xBr0.12+0.32x)121, 0 ≤ x ≤ 0.02 with DMSO as the appropriate solvent. The absorption edge of the material is around 410-430 nm, achieving great transparency to visible light. The structural, optical, and photovoltaic performances of the clear perovskite materials are explored with the variation of Cs contents via CsBr. The relation between thickness, transparency, and optoelectronic properties of the clear perovskite materials along with other physical properties were investigated. The highest photovoltaic conversion efficiency (PCE) of clear perovskite solar cells with 1.5% Cs was achieved to be 0.69% under xenon lamp irradiation at 100 mW/cm2 (1.5 mW/cm2 of UVA within 100 mW/cm2) and 5.24% under 365 nm UV irradiation at 2.4 mW/cm2. Photoresponsivity, external quantum efficiency (EQE), and detectivity were also determined for photodetector applications.

Graded multilayer triple cation perovskites for high speed and detectivity self-powered photodetector via scalable spray coating process.

Rapid advancements in perovskite materials have led to potential applications in various optoelectronic devices, such as solar cells, light-emitting diodes, and photodetectors. Due to good photoelectric properties, perovskite enables low-cost and comparable performance in terms of responsivity, detectivity, and speed to those of the silicon counterpart. In this work, we utilized triple cation perovskite, well known for its high performance, stability, and wide absorption range, which is crucial for broadband photodetector applications. To achieve improved detectivity and faster response time, graded multilayer perovskite absorbers were our focus. Sequential spray deposition, which allows stacked perovskite architecture without disturbing lower perovskite layers, was used to generate single, double, and triple-layer perovskite photodetectors with proper energy band alignment. In this work, we achieved a record on self-powered perovskite photodetector fabricated from a scalable spray process in terms of EQE and responsivity of 65.30% and 0.30 A W-1. The multilayer devices showed faster response speed than those of single-layer perovskite photodetectors with the champion device reaching 70 µs and 88 µs for rising and falling times. The graded band structure and the internal electric field generated from perovskite heterojunction also increase specific detectivity about one magnitude higher in comparison to the single-layer with the champion device achieving 6.82 × 1012 cmHz1/2 W-1.

Electrical Conduction Properties of Hydrogenated Amorphous Carbon Films with Different Structures.

Hydrogenated amorphous carbon (a-C:H) films have optical and electrical properties that vary widely depending on deposition conditions; however, the electrical conduction mechanism, which is dependent on the film structure, has not yet been fully revealed. To understand the relationship between the film structure and electrical conduction mechanism, three types of a-C:H films were prepared and their film structures and electrical properties were evaluated. The sp2/(sp2 + sp3) ratios were measured by a near-edge X-ray absorption fine structure technique. From the conductivity-temperature relationship, variable-range hopping (VRH) conduction was shown to be the dominant conduction mechanism at low temperatures, and the electrical conduction mechanism changed at a transition temperature from VRH conduction to thermally activated band conduction. On the basis of structural analyses, a model of the microstructure of a-C:H that consists of sp2 and sp3-bonded carbon clusters, hydrogen atoms and dangling bonds was built. Furthermore, it is explained how several electrical conduction parameters are affected by the carrier transportation path among the clusters.