Updating the study protocol: Insight 46 - a longitudinal neuroscience sub-study of the MRC National Survey of Health and Development - phases 2 and 3.

BACKGROUND: Although age is the biggest known risk factor for dementia, there remains uncertainty about other factors over the life course that contribute to a person's risk for cognitive decline later in life. Furthermore, the pathological processes leading to dementia are not fully understood. The main goals of Insight 46-a multi-phase longitudinal observational study-are to collect detailed cognitive, neurological, physical, cardiovascular, and sensory data; to combine those data with genetic and life-course information collected from the MRC National Survey of Health and Development (NSHD; 1946 British birth cohort); and thereby contribute to a better understanding of healthy ageing and dementia. METHODS/DESIGN: Phase 1 of Insight 46 (2015-2018) involved the recruitment of 502 members of the NSHD (median age = 70.7 years; 49% female) and has been described in detail by Lane and Parker et al. 2017. The present paper describes phase 2 (2018-2021) and phase 3 (2021-ongoing). Of the 502 phase 1 study members who were invited to a phase 2 research visit, 413 were willing to return for a clinic visit in London and 29 participated in a remote research assessment due to COVID-19 restrictions. Phase 3 aims to recruit 250 study members who previously participated in both phases 1 and 2 of Insight 46 (providing a third data time point) and 500 additional members of the NSHD who have not previously participated in Insight 46. DISCUSSION: The NSHD is the oldest and longest continuously running British birth cohort. Members of the NSHD are now at a critical point in their lives for us to investigate successful ageing and key age-related brain morbidities. Data collected from Insight 46 have the potential to greatly contribute to and impact the field of healthy ageing and dementia by combining unique life course data with longitudinal multiparametric clinical, imaging, and biomarker measurements. Further protocol enhancements are planned, including in-home sleep measurements and the engagement of participants through remote online cognitive testing. Data collected are and will continue to be made available to the scientific community.

Green solvents, materials, and lead-free semiconductors for sustainable fabrication of perovskite solar cells.

Perovskite materials research has received unprecedented recognition due to its applications in photovoltaics, LEDs, and other large area low-cost electronics. The exceptional improvement in the photovoltaic conversion efficiency of Perovskite solar cells (PSCs) achieved over the last decade has prompted efforts to develop and optimize device fabrication technologies for the industrial and commercial space. However, unstable operation in outdoor environments and toxicity of the employed materials and solvents have hindered this proposition. While their optoelectronic properties are extensively studied, the environmental impacts of the materials and manufacturing methods require further attention. This review summarizes and discusses green and environment-friendly methods for fabricating PSCs, particularly non-toxic solvents, and lead-free alternatives. Greener solvent choices are surveyed for all the solar cell films, (i.e. electron and hole transport, semiconductor, and electrode layers) and their impact on thin film quality, morphology and device performance is explored. We also discuss lead content in perovskites, its environmental impact and sequestration routes, and progress in replacing lead with greener alternatives. This review provides an analysis of sustainable green routes in perovskite solar cell fabrication, discussing the impact of each layer in the device stack, via life cycle analysis.

Biological/metal oxide composite transport layers cast from green solvents for boosting light harvesting response of organic photovoltaic cells indoors.

Organic solar cells with biological/metal-oxide electron transport layers (ETLs), consisting of a ZnO compact layer covered by a thin DNA layer, both of which deposited with green solvents (water or water/alcohols mixtures) are presented for application under low intensity indoor lighting. Under white LED lamp (200, 400 lx), photovoltaic cells with P3HT:PC70BM polymer semiconductor blends delivered an average maximum power density (MPD) of 8.7µW cm-2, corresponding to a power conversion efficiency, PCE, of = 8.56% (PCE of best cell was 8.74%). The ZnO/DNA bilayer boosted efficiency by 68% and 13% in relative terms compared to cells made with DNA-only and ZnO-only ETLs at 400 lx. Photovoltaic cells with ZnO/DNA composite ETLs based on PTB7:PC70BM blends, that absorb a broader range of the indoor lighting spectrum, delivered MPDs of 16.2µW cm-2with an estimated average PCE of 14.3% (best cell efficiency of 15.8%) at 400 lx. The best efficiencies for cells fabricated on flexible plastic substrates were 11.9% at 400 lx. This is the first report in which polymer photovoltaics incorporating biological materials have shown to increment performance at these low light levels and work very efficiently under indoor artificial light illumination. The finding can be useful for the production of more bio-compatible photovoltaics as well as bio-sensing devices based on organic semiconductors.

Attributes of High-Performance Electron Transport Layers for Perovskite Solar Cells on Flexible PET versus on Glass.

Electron transport layers (ETLs) play a fundamental role in perovskite solar cells (PSCs) through charge extraction. Here, we developed flexible PSCs on 12 different kinds of ETLs based on SnO2. We show that ETLs need to be specifically developed for plastic substrates in order to attain 15% efficient flexible cells. Recipes developed for glass substrates do not typically transfer directly. Among all the ETLs, ZnO/SnO2 double layers delivered the highest average power conversion efficiency of 14.6% (best cell 14.8%), 39% higher than that of flexible cells of the same batch based on SnO2-only ETLs. However, the cells with a single ETL made of SnO2 nanoparticles were found to be more stable as well as more efficient and reproducible than SnO2 formed from a liquid precursor (SnO2-LP). We aimed at increasing the understanding of what makes a good ETL on polyethylene terephthalate (PET) substrates. More so than ensuring electron transport (as seen from on-current and series resistance analysis), delivering high shunt resistances (R SH) and lower recombination currents (I off) is key to obtain high efficiency. In fact, R SH of PSCs fabricated on glass was twice as large, and I off was 76% lower in relative terms, on average, than those on PET, indicating considerably better blocking behavior of ETLs on glass, which to a large extent explains the differences in average PCE (+29% in relative terms for glass vs PET) between these two types of devices. Importantly, we also found a clear trend for all ETLs and for different substrates between the wetting behavior of each surface and the final performance of the device, with efficiencies increasing with lower contact angles (ranging between ∼50 and 80°). Better wetting, with average contact angles being lower by 25% on glass versus PET, was conducive to delivering higher-quality layers and interfaces. This cognizance can help further optimize flexible devices and close the efficiency gap that still exists with their glass counterparts.

Simple and effective deposition method for solar cell perovskite films using a sheet of paper.

Most laboratories employ spin coating with application of antisolvent to achieve high efficiency in perovskite solar cells. However, this method wastes a lot of material and is not industrially usable. Conversely, large area coating techniques such as blade and slot-die require high precision engineering both for deposition of ink and for gas or for electromagnetic drying procedures that replace, out of necessity, anti-solvent engineering. Here we present a simple and effective method to deposit uniform high-quality perovskite films with a piece of paper as an applicator at low temperatures. We fabricated solar cells on flexible PET substrates manually with 11% power conversion efficiency. Deposition after soaking the sheet of paper in a green antisolvent improved the efficiency by 82% compared to when using dry paper as applicator. This new technique enables manual film deposition without any expensive equipment and has the potential to be fully automated for future optimization and exploitation.

Laser-Scribing Optimization for Sprayed SnO2-Based Perovskite Solar Modules on Flexible Plastic Substrates.

Flexible perovskite solar cells (FPSCs) are prime candidates for applications requiring a highly efficient, low-cost, lightweight, thin, and even foldable power source. Despite record efficiencies of lab-scale flexible devices (19.5% on a 0.1 cm2 area), scalability represents a critical factor toward commercialization of FPSCs. Large-area automized deposition techniques and efficient laser scribing procedures are required to enable a high-throughput production of flexible perovskite modules (FPSMs), with the latter being much more challenging compared to glass substrates. In this work, we introduce the combined concept of laser scribing optimization and automatized spray-coating of SnO2 layers. Based on a systematic variation of the incident laser power and a comprehensive morphological and electrical analysis of laser-based cell interconnections, optimal scribing parameters are identified. Furthermore, spray-coating is used to deposit uniform compact SnO2 films on large-area (>120 cm2) plastic substrates. FPSCs with spray-coated SnO2 show comparable performance as spin-coated cells, delivering up to 15.3% efficiency on small areas under 1 sun illumination. When upscaling to large areas, FPSMs deliver 12% power conversion efficiency (PCE) and negligible hysteresis on 16.8 cm2 and 11.7% PCE on a 21.8 cm2 active area. Our perovskite devices preserved 78% efficiency when the active area increased from 0.1 to 16.8 cm2, demonstrating that our combined approach is an effective strategy for large-area manufacturing of perovskite devices on flexible substrates.

Colour-sensitive conjugated polymer inkjet-printed pixelated artificial retina model studied via a bio-hybrid photovoltaic device.

In recent years, organic electronic materials have been shown to be a promising tool, even transplanted in vivo, for transducing light stimuli to non-functioning retinas. Here we developed a bio-hybrid optoelectronic device consisting of patterned organic polymer semiconductors interfaced with an electrolyte solution in a closed sandwich architecture in order to study the photo-response of photosensitive semiconducting layers or patterns in an environment imitating biological extracellular fluids. We demonstrate an artificial retina model composed of on an array of 42,100 pixels made of three different conjugated polymers via inkjet printing with 110 pixels/mm2 packing density. Photo-sensing through three-colour pixelation allows to resolve incoming light spectrally and spatially. The compact colour sensitive optoelectronic device represents an easy-to-handle photosensitive platform for the study of the photo response of artificial retina systems.

Thermosetting Polyurethane Resins as Low-Cost, Easily Scalable, and Effective Oxygen and Moisture Barriers for Perovskite Solar Cells.

Long-term stability of perovskite solar cells (PSCs) is one of the main issues to be solved for forthcoming commercialization of this technology. In this work, thermosetting polyurethane (PU)-based resins are proposed as effective encapsulants for perovskite solar cells to prevent degradation caused by both moisture and oxygen. Application consists of drop-casting the precursor mixture directly over the devices followed by in situ polymerization, avoiding the use of other adhesives. PUs are cost-effective, lightweight, thermal, and light-stable materials whose mechanical, chemical, and physical properties can be easily tuned by thoughtful choice of their precursor. Encapsulated PSCs show extremely good stability when stored under ambient light (maximum, 1000 lux), controlled humidity (28-65%), and temperature (18-30 °C) by retaining 94% of the initial power conversion efficiency after 2500 h (4 months), whereas control devices lose 90% of their performance after 500 h (T80 = 37 h); once stored according to ISOS-D-1, PU-protected devices showed T80 > 1200 h. Encapsulated devices are stable even when immersed in pure water. The demonstration of PUs as promising solution-processed encapsulant materials for PSCs can pave the way for these to become a cost-effective encapsulation route alternative for future industrialization of this technology.

Coating ZnO nanoparticle films with DNA nanolayers for enhancing the electron extracting properties and performance of polymer solar cells.

Here we present for the first time polymer solar cells that incorporate biological material that show state of the art efficiencies in excess of 8%. The performance of inverted polymer solar cells was improved significantly after deposition of ZnO nanoparticles (ZnO-NPs) together with a thin deoxyribonucleic acid nanolayer and used as an electron extraction layer (EEL). The ZnO-NPs/DNA double layer improved the rectifying ratio, shunt resistance of the cells as well as lowering the work function of the electron-collecting contact. Importantly, the ZnO-NPs/DNA bilayer enhanced the power conversion efficiency of cells considerably compared to cells with EELs made of only DNA (improvement of 56% in relative terms) or only ZnO-NPs (improvement of 19% in relative terms) reaching a best power conversion efficiency of 8.5%. The ZnO-NPs/DNA double layer cells also outperformed ones made with one of the most efficient previous synthetic composite EELs (i.e. ZnO/PEIE(poly(ethyleneimine)-ethoxylated)). Since all fabrication procedures were carried out at low (<150 °C) or room temperature, we have applied the findings to flexible substrates as well as on glass obtaining a high PCE of 7.2%. The solar cells with the biological/metal-oxide composite EELs also delivered an improvement in the stability (∼20% in relative term) compared to that with ZnO-NPs only. All these findings show that natural materials, in this case DNA, the premium biological material, can be incorporated in organic semiconductor devices in tandem with inorganic devices delivering uncompromising levels of performance as well as significant improvements.

Relativistic deflection of background starlight measures the mass of a nearby white dwarf star.

Gravitational deflection of starlight around the Sun during the 1919 total solar eclipse provided measurements that confirmed Einstein's general theory of relativity. We have used the Hubble Space Telescope to measure the analogous process of astrometric microlensing caused by a nearby star, the white dwarf Stein 2051 B. As Stein 2051 B passed closely in front of a background star, the background star's position was deflected. Measurement of this deflection at multiple epochs allowed us to determine the mass of Stein 2051 B-the sixth-nearest white dwarf to the Sun-as 0.675 ± 0.051 solar masses. This mass determination provides confirmation of the physics of degenerate matter and lends support to white dwarf evolutionary theory.

Parkinsonism and Vitamin C Deficiency.

Patients with vitamin C deficiencies and parkinsonism can show rapid improvement with vitamin C replacement therapy.

Solid state perovskite solar modules by vacuum-vapor assisted sequential deposition on Nd:YVO4 laser patterned rutile TiO2 nanorods.

The past few years have witnessed remarkable progress in solution-processed methylammonium lead halide (CH3NH3PbX3, X = halide) perovskite solar cells (PSCs) with reported photoconversion efficiency (η) exceeding 20% in laboratory-scale devices and reaching up to 13% in their large area perovskite solar modules (PSMs). These devices mostly employ mesoporous TiO2 nanoparticles (NPs) as an electron transport layer (ETL) which provides a scaffold on which the perovskite semiconductor can grow. However, limitations exist which are due to trap-limited electron transport and non-complete pore filling. Herein, we have employed TiO2 nanorods (NRs), a material offering a two-fold higher electronic mobility and higher pore-filing compared to their particle analogues, as an ETL. A crucial issue in NRs' patterning over substrates is resolved by using precise Nd:YVO4 laser ablation, and a champion device with η ∼ 8.1% is reported via a simple and low cost vacuum-vapor assisted sequential processing (V-VASP) of a CH3NH3PbI3 film. Our experiments showed a successful demonstration of NRs-based PSMs via the V-VASP technique which can be applied to fabricate large area modules with a pin-hole free, smooth and dense perovskite layer which is required to build high efficiency devices.

Vertical TiO2 Nanorods as a Medium for Stable and High-Efficiency Perovskite Solar Modules.

Perovskite solar cells employing CH3NH3PbI3-xClx active layers show power conversion efficiency (PCE) as high as 20% in single cells and 13% in large area modules. However, their operational stability has often been limited due to degradation of the CH3NH3PbI3-xClx active layer. Here, we report a perovskite solar module (PSM, best and av. PCE 10.5 and 8.1%), employing solution-grown TiO2 nanorods (NRs) as the electron transport layer, which showed an increase in performance (∼5%) even after shelf-life investigation for 2500 h. A crucial issue on the module fabrication was the patterning of the TiO2 NRs, which was solved by interfacial engineering during the growth process and using an optimized laser pulse for patterning. A shelf-life comparison with PSMs built on TiO2 nanoparticles (NPs, best and av. PCE 7.9 and 5.5%) of similar thickness and on a compact TiO2 layer (CL, best and av. PCE 5.8 and 4.9%) shows, in contrast to that observed for NR PSMs, that PCE in NPs and CL PSMs dropped by ∼50 and ∼90%, respectively. This is due to the fact that the CH3NH3PbI3-xClx active layer shows superior phase stability when incorporated in devices with TiO2 NR scaffolds.

Luminescent Mechanochromism in a Gold(I)-Copper(I) N-Heterocyclic Carbene Complex.

The silver(I) species [Ag(benzim(CH2py)2)2]PF6 (1) was prepared by refluxing the ligand precursor [H(benzim(CH2py)2)2]PF6 with Ag2O and aqueous sodium hydroxide in dichloromethane. Simple transmetalation of 1 with tetrahydrothiophenegold(I) chloride forms the gold(I) analogue [Au(benzim(CH2py)2)2]PF6 (2). The addition of 2 equiv of [Cu(NCCH3)4]PF6 to 2 in acetonitrile produces a blue-luminescent, trimetallic complex, [AuCu2(benzim(CH2py)2)2(NCCH3)4](PF6)3·2CH3CN (3·2CH3CN). When blue-luminescent 3·2CH3CN is exposed to air, the complex loses four acetonitrile molecules, and the emission of the desolvated complex (4) appears aquamarine. Crystallization of 4 from different solvents produces the complexes [AuCu2(benzim(CH2py)2)2](PF6)3 (5) and [AuCu2(benzim(CH2py)2)2(NCCH2CH3)2](PF6)3 (6). Upon grinding, both 3·2CH3CN and 4 exhibit mechanochromic transformations to a yellow-luminescent powder (ground-4). The reversible mechanochromic transformation of 3·2CH3CN to ground-4 is a crystalline-to-amorphous conversion accompanied by partial desolvation. The luminescent mechanochromism of 4 to ground-4 is an "amorphous-to-amorphous" process and does not require solvent loss. In addition to their mechanochromic properties, both 3·2CH3CN and 4 exhibit luminescent thermochromism through desolvation to form a weak luminescent powder (7).

Neuropsychiatric scurvy.

BACKGROUND: Scurvy is a disease with well-known peripheral symptoms, such as bleeding and pain. METHODS: The clinical and historical evidence for a distinct form of scurvy affecting the central nervous system, called neuropsychiatric scurvy, is reviewed. Pathophysiologic factors are described, as well as its diagnosis and management.

Ascorbate- and zinc-responsive parkinsonism.

OBJECTIVE: To report a case of Parkinsonism rapidly responsive to intravenous replacement of vitamin C and zinc. CASE SUMMARY: A 66-year-old man with Parkinsonism, pleural effusion, and bipolar disorder was found to have low serum vitamin C and zinc levels. Intravenous replacement of these micronutrients led to resolution of the movement disorder in less than 24 hours. DISCUSSION: Parkinsonism has been associated with vitamin C deficiency, and recent cases of scurvy complicated by Parkinsonism have responded well to intravenous replacement of vitamin C. In this case, deficiency of zinc may have contributed to the development of a movement disorder. The likely pathophysiology of, and treatment recommendations for, Parkinsonism linked to deficiencies of vitamin C and zinc are reviewed. CONCLUSIONS: Whereas vitamin C has a strong link with Parkinsonism, the potential role of zinc has only been suspected. This case report highlights some of the potential links between zinc deficiency and Parkinsonism.