Heavy pnictogen chalcohalides for efficient, stable, and environmentally friendly solar cell applications.

Solar cell technology is an effective solution for addressing climate change and the energy crisis. Therefore, many researchers have investigated various solar cell absorbers that convert Sunlight into electric energy. Among the different materials researched, heavy pnictogen chalcohalides comprising heavy pnictogen cations, such as Bi3+and Sb3+, and chalcogen-halogen anions have recently been revisited as emerging solar absorbers because of their potential for efficient, stable, and low-toxicity solar cell applications. This review explores the recent progress in the applications of heavy pnictogen chalcohalides, including oxyhalides and mixed chalcohalides, in solar cells. We categorize them into material types based on their common structural characteristics and describe their up-to-date developments in solar cell applications. Finally, we discuss their material imitations, challenges for further development, and possible strategies for overcoming them.

Light-Emitting Conjugated Organic Polymer as an Efficient Fluorescent Probe for Cu2+ Ions Detection and Cell Imaging.

Conjugated organic polymers (COPs) have been excellent candidates because the conjugated structure occupied π structure that is useful to develop light-emitting materials. However, most COPs emitt weak luminescence owing to the H-aggregation effect. Light-emitting conjugated organic polymers (LCOP-1) possess rich butyl groups anchored in the skeleton to enhance light-emitting activity via reducing the H-aggregation effect. Owing to abundant hydroxyl and nitrogen atoms, LCOP-1 exhibits high sensitivity, selectivity, and fast response to Cu2+ ions within 1 min in comparison with the cations of Na+ , Mg2+ , Al3+ , Zn2+ , Cd2+ , Ni2+ , Cr3+ , Hg2+ , Fe3+ , Fe2+ , Pb2+ , Co2+ , etc. The detection limit can be down to nanomolar. Moreover, the sensor exhibits detection toward Cu2+ ions via a naked eye colorful change from pale-yellow to yellowish-brown. Furthermore, the light-emitting probe also successfully achieves the detection of Cu2+ ions in cells without cytotoxicity, indicating its great potentials in biological function.

Constructing Stable and Porous Covalent Organic Frameworks for Efficient Iodine Vapor Capture.

Covalent organic frameworks (COF) with periodic porous structures and tunable functionalities are a new class of crystalline polymers connected via strong covalent bonds. Constructing COF materials with high stability and porosity is attracting and essential for COFs' further functional exploration. In this work, two new covalent organic frameworks (TTA-TMTA-COF and TTA-FMTA-COF) with high surface area, large pore volume, and excellent chemical stability toward harsh conditions are designed and synthesized by integrating the methoxy functional groups into the networks. Both two COFs are further employed for iodine removal since radioactive iodine in nuclear waste has seriously threatened the natural environment and human health. TTA-TMTA-COF and TTA-FMTA-COF can capture 3.21 and 5.07 g g-1 iodine, respectively. Notably, the iodine capture capacity for iodine of TTA-FMTA-COF does not show any decline after being recycled five times. These results demonstrate both COFs possess ultrahigh capacity and excellent recyclability.

Efficient and Stable Antimony Selenoiodide Solar Cells.

Although antimony selenoiodide (SbSeI) exhibits a suitable bandgap as well as interesting physicochemical properties, it has not been applied to solar cells. Here the fabrication of SbSeI solar cells is reported for the first time using multiple spin-coating cycles of SbI3 solutions on Sb2Se3 thin layer, which is formed by thermal decomposition after depositing a single-source precursor solution. The performance exhibits a short-circuit current density of 14.8 mA cm-2, an open-circuit voltage of 473.0 mV, and a fill factor of 58.7%, yielding a power conversion efficiency (PCE) of 4.1% under standard air mass 1.5 global (AM 1.5 G, 100 mW cm-2). The cells retain ≈90.0% of the initial PCE even after illuminating under AM 1.5G (100 mW cm-2) for 2321 min. Here, a new approach is provided for combining selenide and iodide as anions, to fabricate highly efficient, highly stable, green, and low-cost solar cells.

Strain Tuning via Larger Cation and Anion Codoping for Efficient and Stable Antimony-Based Solar Cells.

Strain induced by lattice distortion is one of the key factors that affect the photovoltaic performance via increasing defect densities. The unsatisfied power conversion efficiencies (PCEs) of solar cells based on antimony chalcogenides (Sb-Chs) are owing to their photoexcited carriers being self-trapped by the distortion of Sb2S3 lattice. However, strain behavior in Sb-Chs-based solar cells has not been investigated. Here, strain tuning in Sb-Chs is demonstrated by simultaneously replacing Sb and S with larger Bi and I ions, respectively. Bi/I codoped Sb2S3 cells are fabricated using poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7-(2,1,3-enzothiadiazole)] as the hole-transporting layer. Codoping reduced the bandgap and rendered a bigger tension strain (1.76 × 10-4) to a relatively smaller compression strain (-1.29 × 10-4). The 2.5 mol% BiI3 doped Sb2S3 cell presented lower trap state energy level than the Sb2S3 cell; moreover, this doping amount effectively passivated the trap states. This codoping shows a similar trend even in the low bandgap Sb2(SxSe1-x)3 cell, resulting in 7.05% PCE under the standard illumination conditions (100 mW cm-2), which is one of the top efficiencies in solution processing Sb2(SxSe1-x)3 solar cells. Furthermore, the doped cells present higher humidity, thermal and photo stability. This study provides a new strategy for stable Pb-free solar cells.

Efficient Solar Cells Employing Light-Harvesting Sb0.67 Bi0.33 SI.

Sb1- x Bix SI, an isostructural material with the well-known quasi-1D SbSI, possesses good semiconductive and ferroelectric properties but is not applied in solar cells. Herein, solar cells based on alloyed Sb0.67 Bi0.33 SI (ASBSI) as a light harvester are fabricated. ASBSI is prepared through the reaction of bismuth triiodide in N,N-dimethylformamide solution with an antimony trisulfide film deposited on a mesoporous (mp)-TiO2 electrode via chemical bath deposition at 250 °C under an argon or nitrogen atmosphere; the alloy exhibits a promising bandgap (1.62 eV). The best performing cell fabricated with poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7-(2,1,3-benzothiadiazole)] as the hole-transporting layer shows 4.07% in a power conversion efficiency (PCE) under the standard illumination conditions of 100 mW cm-2 . The unencapsulated cells exhibit good comprehensive stability with retention of 92% of zjr initial PCE under ambient conditions of 60% relative humidity over 360 h, 93% after 1 sun illumination for 1254 min, and 92% after storage at 85 °C in air for 360 h.

Stabilization of Lead-Tin-Alloyed Inorganic-Organic Halide Perovskite Quantum Dots.

Recently, lead-tin-based alloyed halide perovskite quantum dots (QDs) with improved stability and less toxicity have been introduced. However, the perovskite QDs containing tin are still unstable and exhibit low photoluminescence quantum yields (PLQYs), owing to the presence of defects in the alloyed system. Here, we have attempted to introduce sulfur anions (S2-) into the host lattice (MAPb0.75Sn0.25Br3) as a promising route to stable alloyed perovskite QDs with improved stability and PLQY. In this study, we used elemental sulfur as a sulfur precursor. The successful incorporation of sulfur anions into the host lattice resulted in a highly improved PLQY (>75% at room temperature), which is believed to be due to a reduction in the defect-related non-radiative recombination centers present in the host lattice. Furthermore, we found that the emission property could be tuned between the bright green and cyan-bluish regions without compromising on color quality. This work invigorates the perovskite research community to prepare stable, bright, and color-tunable alloyed inorganic-organic perovskite QDs without compromising on their phases and color quality, which can lead to considerable advances in display technology.

Nanochannel-Assisted Perovskite Nanowires: From Growth Mechanisms to Photodetector Applications.

Growing interest in hybrid organic-inorganic lead halide perovskites has led to the development of various perovskite nanowires (NWs), which have potential use in a wide range of applications, including lasers, photodetectors, and light-emitting diodes (LEDs). However, existing nanofabrication approaches lack the ability to control the number, location, orientation, and properties of perovskite NWs. Their growth mechanism also remains elusive. Here, we demonstrate a micro/nanofluidic fabrication technique (MNFFT) enabling both precise control and in situ monitoring of the growth of perovskite NWs. The initial nucleation point and subsequent growth path of a methylammonium lead iodide-dimethylformamide (MAPbI3·DMF) NW array can be guided by a nanochannel. In situ UV-vis absorption spectra are measured in real time, permitting the study of the growth mechanism of the DMF-mediated crystallization of MAPbI3. As an example of an application of the MNFFT, we demonstrate a highly sensitive MAPbI3-NW-based photodetector on both solid and flexible substrates, showing the potential of the MNFFT for low-cost, large-scale, highly efficient, and flexible optoelectronic applications.

Mixed Sulfur and Iodide-Based Lead-Free Perovskite Solar Cells.

The use of divalent chalcogenides and monovalent halides as anions in a perovskite structure allows the introduction of 3+ and 4+ charged cations in the place of the 2+ metal cations. Herein we report for the first time on the fabrication of solar cells exploiting methylammonium antimony sulfur diiodide (MASbSI2) perovskite structures, as light harvesters. The MASbSI2 was prepared by annealing under mild temperature conditions, via a sequential reaction between antimony trisulfide (Sb2S3), which is deposited by the chemical bath deposition (CBD) method, antimony triiodide (SbI3), and methylammonium iodide (MAI) onto a mesoporous TiO2 electrode, and then annealed at 150 °C in an argon atmosphere. The solar cells fabricated using MASbSI2 exhibited power conversion efficiencies (PCE) of 3.08%, under the standard illumination conditions of 100 mW/cm2.

Highly Sensitive and Broadband Organic Photodetectors with Fast Speed Gain and Large Linear Dynamic Range at Low Forward Bias.

Photodetectors with high photoelectronic gain generally require a high negative working voltage and a very low environment temperature. They also exhibit low response speed and narrow linear dynamic range (LDR). Here, an organic photodiode is demonstrated, which shows a large amount of photon to electron multiplication at room temperature with highest external quantum efficiency (EQE) from ultraviolet (UV) to near-infrared region of 5.02 × 103 % (29.55 A W-1 ) under a very low positive voltage of 1.0 V, accompanied with a fast response speed and a high LDR from 10-7 to 101 mW cm-2 . At a relatively high positive bias of 10 V, the EQE is up to 1.59 × 105 % (936.05 A W-1 ). Inversely, no gain is found at negative bias. The gain behavior is exactly similar to a bipolar phototransistor, which is attributed to the photoinduced release of accumulated carriers. The devices at a low voltage exhibit a normalized detectivity (D*) over 1014 Jones by actual measurements, which is about two or three order of magnitudes higher than that of the highest existing photodetectors. These pave a new way for realization of high sensitive detectors with fast response toward the single photon detection.

Aligned nanofibers as an interfacial layer for achieving high-detectivity and fast-response organic photodetectors.

We report that aligned nanofibers (ANs) prepared by electrostatic spinning technology as an interfacial layer can significantly enhance the performance of inverted organic photodetectors. With the insertion of ANs of titanium dioxide (TiO2), the optimized organic photodetectors had a highest detectivity of 2.93 × 10(13) Jones at zero bias, which is about 3 times higher than that of a similar organic photodetector without ANs and also markedly higher than that of traditional silicon photodetectors. The performance of the devices with different TiO2 ANs as the interfacial layer was investigated, and the results exhibited that photodetectors with one-way ANs had the highest detectivity and shortest response time. This work provides a new application of nanofibers fabricated by a simple and controllable process in high-performance organic photodetectors.