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Despite the rapid improvement of photovoltaic (PV) efficiency in hybrid organic-inorganic metal halide perovskites (HOIPs), the fabrication procedure of a compact thin film in a large-area application is still a tedious work. Apart from the quality of the thin film, the stability of the perovskite materials and the expensive organic hole transport layer (HTL) within the HOIP-based PV device are the major issues that need to be addressed prior to their commercialization. Herein, a unique glass rod-based facile fabrication technique for producing a compact and stable thin film utilizing a mixed-halide-based perovskite precursor solution is demonstrated. The fabricated devices deliver high photoconversion efficiency (PCE) without the use of any HTL and show an excellent stability under ambient conditions. By varying the organic CH 3 NH 3 I (MAI) and inorganic PbBr 2 content, perovskite materials with different dimensions, i.e., 3D, 2D, and 1D, are synthesized to produce an active layer for PV devices. Although a 2D single-halide perovskite is reported earlier, herein two different mixed-halide 2D perovskites, i.e., MA 2 PbI 2 Br 2 and MAPb 2 IBr 4 , are synthesized successfully, and their performance is compared in detail along with that of 1D and 3D mixed-halide perovskites. The facile synthesized mixed-halide 2D-based MA 2 PbI 2 Br 2 perovskite shows a PCE of 10.14% with a high stability of 92% after 100 days without encapsulation, which is much superior as compared to that of the mixed-halide 3D MAPbIBr 2 . The semiconducting behavior as well as the nature of the bandgap of the synthesized compounds is examined by pursuing density functional theory calculations. Specifically, the role of iodine doping to modify the electronic band structure is investigated, and introduction of iodine is found to reduce the effective masses of both electrons and holes in the perovskite material.

Here, we report the design and synthesis of a redox-active multifunctional ionic porous organic polymer iPOP-Bpy with exchangeable Br - ions, incorporating viologen as a redox-active building block. The material shows not only excellent iodine uptake capacity in the vapor phase (540 wt %) but also in the organic (1009.77 mg g -1 ) and aqueous phases (3921.47 mg g -1 ) with very fast adsorption kinetics in all cases. The material also shows its utility in being used as a solid-state NH 3 vapor sensor as it shows very fast color switching in the presence of NH 3 vapor. Furthermore, the material found application as a p-type complementary electrochromic electrode and was fabricated into a bilayer device. Excellent coloration efficiency, high switching speed, and good color contrast were obtained as investigated using bias-dependent optical and spectroelectrochemical studies, paving the way for fabricating power-efficient solid-state electrochromic devices.

Hybrid organometallic halide perovskite-based semitransparent solar cell research has garnered significant attention recently due to their promising applications for smart windows, tandem devices, wearable electronics, displays, and sustainable internet-of-things. Though considerable progress has been made, stability, controlling the crystalline qualities, and growth orientation in perovskite thin films play crucial roles in improving the photovoltaic (PV) performance. Recently, strain modulation within the perovskite gathers an immense interest that is achieved by the ex situ process. However, little work is reported on in situ strain modulation, which is presented here. Apart from the challenges in the fabrication of high-efficiency perovskite solar cell (PSC) devices under ambient conditions, the stability of organic hole-transporting materials needs urgent attention. Herein, a single-step deposition of formamidiniumchloride (FACl)-mediated CH 3 NH 3 PbI 3 (MAPbI 3 ) thin films without an inert atmosphere and CuI as the inorganic hole-transporting material is demonstrated for their potential application toward semitransparent PSCs. The FACl amount in MAPbI 3 (mg/mL) plays a critical role in controlling the crystallinity, growth orientations, and in situ strains, which modulate the charge carrier transport dynamics, thereby improving the efficiency of the PSC device. A photoconversion efficiency of 16.01% has been achieved from MAPbI 3 with 20 mg/mL of FACl additive incorporation. The modification of the structural, electronic, and optical properties and the origin of strain in the as-synthesized MAPbI 3 domains due to the addition of FACl are further validated with experimental findings in detail using density functional theory simulations.

Robust processes to fabricate densely packed high-aspect-ratio (HAR) vertical semiconductor nanostructures are important for applications in microelectronics, energy storage and conversion. One of the main challenges in manufacturing these nanostructures is pattern collapse, which is the damage induced by capillary forces from numerous solution-based processes used during their fabrication. Here, using an array of vertical silicon (Si) nanopillars as test structures, we demonstrate that pattern collapse can be greatly reduced by a solution-phase deposition method to coat the nanopillars with self-assembled monolayers (SAMs). As the main cause for pattern collapse is strong adhesion between the nanopillars, we systematically evaluated SAMs with different surface energy components and identified H-bonding between the surfaces to have the largest contribution to the adhesion. The advantage of the solution-phase deposition method is that it can be implemented before any drying step, which causes patterns to collapse. Moreover, after drying, these SAMs can be easily removed using a gentle air-plasma treatment right before the next fabrication step, leaving a clean nanopillar surface behind. Therefore, our approach provides a facile and effective method to prevent the drying-induced pattern collapse in micro- and nanofabrication processes.

Thiolated dendritic mesoporous silica nanoparticles (T-DMSNs) with ultrahigh density of thiol groups (284.6 ± 9 μmol g -1 ) are synthesized and used to load gold nanoparticles with tunable sizes (1.2-2.7 nm) and high content (34.0 wt %). It is demonstrated that the size of gold nanoparticles has a significant impact on their peroxidase-mimicking activity. At an optimized size of 1.9 nm, T-DMSNs@Au exhibits the highest activity. Our contribution provides new insights into the rational design of nanozymes for future applications.

Semiconducting conjugated oligomers having same end group (N-ethylrhodanine) but different central core (thiophene: OT-T, bithiophene: OT-BT, thienothiophene: OT-TT) connected through thiophene pi-linker (alkylated terthiophene) were synthesized for solution processable bulk-heterojunction solar cells. The effect of the incorporation of an extra thiophene to the central thiophene unit either through C-C bond linkage to form bithiophene or by fusing two thiophenes together to form thienothiophene on the optoelectronic properties and photovoltaic performances of the oligomers were studied in detail. Flash photolysis time-resolved microwave conductivity (FP-TRMC) technique shows OT-TT has significantly higher photoconductivity than OT-T and OT-BT implying that the former can outperform the latter two derivatives by a wide margin under identical conditions in a bulk-heterojunction solar cell device. However, the initial photovoltaic devices fabricated from all three oligomers (with PC71BM as the acceptor) gave power conversion efficiencies (PCEs) of about 0.7%, which was counterintuitive to the TRMC observation. By using TRMC results as a guiding tool, solution engineering was carried out; no remarkable changes were seen in the PCE of OT-T and OT-BT. On the other hand, 5-fold enhancement in the device efficiency was achieved in OT-TT (PCE: 3.52%, VOC: 0.80 V, JSC: 8.74 mA cm(-2), FF: 0.50), which was in correlation with the TRMC results. The structure-property correlation and the fundamental reasons for the improvement in device performance upon solvent engineering were deduced through UV-vis absorption, atomic force microscopy, bright-field transmission electron microscopy, photoluminescence quenching analysis and two-dimensional grazing incidence X-ray diffraction studies.

We have sputtered Zn onto quasi-one-dimensional ZnO nanowires (NWs) in order to investigate the effect of Zn diffusion on the photoluminescence and photoconduction properties of ZnO NWs. Elemental mapping clearly indicates higher Zn concentration in the NWs due to diffusion of Zn. The Zn-sputtered NWs show an enhanced ultraviolet emission with 7 nm red shift. Since the ionization energy of Zni is 51 meV, the enhanced PL emission with a red shift is correlated to the coupling between free exciton and zinc interstitials (Zni) defects. The photocurrent transients show almost 20 times more photocurrent generation in Zn/ZnO NWs compared to the as-grown NWs. In contrast, the thin film shows no significant change in the photoluminescence and photoconductivity. Based on the photoconductivity and photoluminescence results, we predict that Zn diffusion in the NWs occurs easily compared to the films because of the smaller dimensions of the NWs.