Defect Passivation through (α-Methylguanido)acetic Acid in Perovskite Solar Cell for High Operational Stability.

Defect passivation has become essential in improving efficiency and stability in perovskite solar cells. Here, we report the use of (α-methylguanido)acetic acid, also known as creatine, as a passivation molecule. It is employed both as an additive and as a surface passivation layer of perovskite thin films, given its multiple functional groups, which could address different defect sites, and its size, which could inherently affect the material structure. We prove that the surface passivation is more efficiently working by removing vulnerable defects on the surface. Hole and electron defect densities were reduced, leading to the highest power conversion efficiency of 22.6%. In addition, it can effectively protect the perovskite thin film and improve the operational stabilities in high thermal (85 °C) and humid conditions (50% relative humidity), suggesting a strong stability of the surface passivation layer.

High External Photoluminescence Quantum Yield in Tin Halide Perovskite Thin Films.

We show that pristine thin films made of tin halide perovskite have external photoluminescence quantum yield comparable to that of lead halide perovskite, i.e., the material in use to prepare state-of-the-art perovskite solar cells.

Perovskite/Hole Transport Layer Interface Improvement by Solvent Engineering of Spiro-OMeTAD Precursor Solution.

Perovskite solar cells (PSCs) are one of the most promising emerging energy-conversion technologies because of their high power conversion efficiencies (PCEs) and potentially low fabrication cost. To improve PCE, it is necessary to develop PSCs with good interfacial engineering to reduce the trap states and carrier transport barriers present at the various interfaces of the PSCs' architecture. This work reports a facile method to improve the interface between the perovskite absorber layer and the hole transport layer (HTL) by adding a small amount of acetonitrile (ACN) in the Spiro-OMeTAD precursor solution. This small amount of ACN dissolves the surface of the perovskite layer, allowing the formation of an interdiffusion structure between perovskite and Spiro-OMeTAD layers. This modification allows for an improved electrical contact, enhanced collection of holes, and reduced recombination losses at the interface between the perovskite and Spiro-OMeTAD layers and, consequently, enhances the PCE. A maximum PCE of 19.7% with low hysteresis and a steady-state power conversion efficiency of 19.0% is obtained for optimized PSCs.

NiMoFe and NiMoFeP as Complementary Electrocatalysts for Efficient Overall Water Splitting and Their Application in PV-Electrolysis with STH 12.3.

Complementary water splitting electrocatalysts used simultaneously in the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) can simplify water splitting systems. Herein, earth-abundant NiMoFe (NMF) and phosphorized NiMoFeP (NMFP) are synthesized as complementary overall water splitting (OWS) catalysts. First, NMF is tested as both the HER and OER promoter, which exhibits low overpotentials of 68 (HER) and 337 mV (OER). A quaternary NMFP is then prepared by simple phosphorization of NMF, which shows a much lower OER overpotential of 286 mV. The enhanced OER activity is attributed to the unique surface/core structure of NMFP. The surface phosphate acts as a proton transport mediator and expedites the rate-determining step. With the application of OER potential, the NMFP surface is composed of Ni(OH)2 and FeOOH, active sites for OER, but the inner core consists of Ni, Mo, and Fe metals, serving as a conductive electron pathway. OWS with NMF-NMFP requires an applied voltage of 1.452 V to generate 10 mA cm-2 , which is one of the lowest values among OWS results with transition-metal-based electrocatalysts. Furthermore, the catalysts are combined with tandem perovskite solar cells for photovoltaic (PV)-electrolysis, producing a high solar-to-hydrogen (STH) conversion efficiency of 12.3%.

Gradated Mixed Hole Transport Layer in a Perovskite Solar Cell: Improving Moisture Stability and Efficiency.

We demonstrate a simple and facile way to improve the efficiency and moisture stability of perovskite solar cells using commercially available hole transport materials, 2,2',7,7'-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9'-spirobifluorene (spiro-OMeTAD) and poly(3-hexylthiophene) (P3HT). The hole transport layer (HTL) composed of mixed spiro-OMeTAD and P3HT exhibited favorable vertical phase separation. The hydrophobic P3HT was more distributed near the surface (the air atmosphere), whereas the hydrophilic spiro-OMeTAD was more distributed near the perovskite layer. This vertical separation resulted in improved moisture stability by effectively blocking moisture in air. In addition, the optimized composition of spiro-OMeTAD and P3HT improved the efficiency of the solar cells by enabling fast intramolecular charge transport. In addition, a suitable energy level alignment facilitated charge transfer. A device fabricated using the mixed HTL exhibited enhanced performance, demonstrating 18.9% power conversion efficiency and improved moisture stability.

Green-Solvent-Processable, Dopant-Free Hole-Transporting Materials for Robust and Efficient Perovskite Solar Cells.

In addition to having proper energy levels and high hole mobility (µh) without the use of dopants, hole-transporting materials (HTMs) used in n-i-p-type perovskite solar cells (PSCs) should be processed using green solvents to enable environmentally friendly device fabrication. Although many HTMs have been assessed, due to the limited solubility of HTMs in green solvents, no green-solvent-processable HTM has been reported to date. Here, we report on a green-solvent-processable HTM, an asymmetric D-A polymer (asy-PBTBDT) that exhibits superior solubility even in the green solvent, 2-methylanisole, which is a known food additive. The new HTM is well matched with perovskites in terms of energy levels and attains a high µh (1.13 × 10-3 cm2/(V s)) even without the use of dopants. Using the HTM, we produced robust PSCs with 18.3% efficiency (91% retention after 30 days without encapsulation under 50%-75% relative humidity) without dopants; with dopants (bis(trifluoromethanesulfonyl) imide and tert-butylpyridine, a 20.0% efficiency was achieved. Therefore, it is a first report for a green-solvent-processable hole-transporting polymer, exhibiting the highest efficiencies reported so far for n-i-p devices with and without the dopants.

Enhanced Efficiency and Stability of an Aqueous Lead-Nitrate-Based Organometallic Perovskite Solar Cell.

We investigate the stability of an active organometallic perovskite layer prepared from a two-step solution procedure, including spin coating of aqueous lead nitrate (Pb(NO3)2) as a Pb2+ source and sequential dipping into a methylammonium iodide (CH3NH3I) solution. The conversion of CH3NH3PbI3 from a uniform Pb(NO3)2 layer generates PbI2-free and large-grain perovskite crystallites owing to an intermediate ion-exchange reaction step, resulting in improved humidity resistance and, thereby, improved long-term stability with 93% of the initial power conversion efficiency (PCE) after a period of 20 days. The conventional fast-converted PbI2-dimethylformamide solution system leaves small amounts of intrinsic PbI2 residue on the resulting perovskite and MAPbI3 crystallites with uncontrollable sizes. This accelerates the generation of PbI2 and the decomposition of the perovskite layer, resulting in poor stability with less than 60% of the initial PCE after a period of 20 days.

A Case of Ciliated Foregut Cyst of the Gallbladder.

Congenital cysts of the gallbladder are extremely rare, hence only a few ciliated foregut cysts of gallbladder have been reported. We report a case of a 20-year-old woman presenting with mild right upper quadrant abdominal discomfort, with normal levels of serum bilirubin and liver function tests. Abdominal ultrasonography revealed a well-defined cystic mass measured about 2 cm attached to the neck of gallbladder, with internal echogenic debris suggesting a complicated cyst, such as a hemorrhagic cyst. Abdominal computed tomography and magnetic resonance cholangiopancreatography revealed similar findings. Laparoscopic cholecystectomy showed a slightly distended gallbladder. The size of cyst on the neck was 1.6×1.2 cm, and it contained mucosa lined by ciliated pseudostratified columnar epithelium and underlying smooth muscle layers. Histopathology identified a ciliated foregut cyst of gallbladder.

A benzodithiophene-based novel electron transport layer for a highly efficient polymer solar cell.

We designed and synthesized a novel conjugated polyelectrolyte (CPE), poly{3-[2-[4,8-bis(2-ethyl-hexyloxy)-6-methyl-1,5-dithia-s-indacen-2-yl]-9-(3-dimethylamino-propyl)-7-methyl-9H-fluoren-9-yl]-propyl}-dimethyl-amine (PBN). We employed PBN as an electron-transporting layer on a ZnO layer and constructed a highly efficient, inverted structure device consisting of a mixture of poly({4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl}{3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl}) (PTB7) and PC70BM, achieving a high power conversion of up to 8.6%, constituting a 21.1% improvement over the control device performance (7.1%) prepared without a PBN layer. This result was ascribed to the reduced interfacial resistance and the improved charge transport and collection through the PBN electron transport layer.