Chemically Welding Silver Nanowires toward Transferable and Flexible Transparent Electrodes in Heaters and Double-Sided Perovskite Solar Cells.

Silver nanowires (AgNWs) are important materials for flexible transparent electrodes (FTEs). However, the loose stacking of nanowire junctions greatly affects the electric conductivity across adjacent nanowires. Soldering can effectively reduce the wire-wire contact resistance of AgNWs by epitaxially depositing nanosolders at the junctions, but the process normally needs to be performed with high energy consumption. In this work, we proposed a simple room-temperature method to achieve precise welding of junctions by adjusting the wettability of the soldered precursor solution on the surfaces of AgNWs. The nanoscale welding at nanowire cross junctions forms efficient conductive networks. Furthermore, reduced graphene oxide (rGO) was used to improve the stability of FTEs by wrapping the rGO around the AgNW surface. The obtained FTE shows a figure-of-merit (FoM) of up to 439.3 (6.5 Ω/sq at a transmittance of 88%) and has significant bending stability and environmental and acidic stability. A flexible transparent heater was successfully constructed, which could reach up to 160 °C within a short response time (43 s) and exhibit excellent switching stability. When laminating this FTE onto half perovskite solar cells as the top electrodes, the obtained double-side devices achieved power conversion efficiencies as high as 16.15% and 13.91% from each side, pointing out a convenient method for fabricating double-sided photovoltaic devices.

Strain Relaxation on Perovskite Surface via Light-Enhanced Ionic Homogeneity.

The efficiency and stability of perovskite solar cells (PSCs) can be either deteriorated or enhanced by strain at interfaces, which is sensitive to various external conditions, particularly light illumination. Here we investigated the vertical strain distribution in perovskite films synthesized under light illumination with various wavelengths. The films were formed by reacting formamidinium iodide (FAI)/methylammonium chloride (MACl) vapor with vapor-deposited PbI2 (CsBr) films. Strain in the films was evaluated with incident-angle-dependent grazing-incidence wide-angle X-ray scattering, which showed out-of-plane compressive and in-plane tensile strains, particularly on the surface. Short-wavelength light relaxed the strain on the perovskite surface via promotion of ionic diffusion, including FA, MA, Cs, and I, to reach vertical ionic homogeneity. With the charge trap concentration being reduced, both the efficiency and stability were greatly improved. This finding provides deep insight into the effect of light on strain in PSCs.

Advances in the Electrocatalytic Hydrogen Evolution Reaction by Metal Nanoclusters-based Materials.

With the development of renewable energy systems, clean hydrogen is burgeoning as an optimal alternative to fossil fuels, in which its application is promising to retarding the global energy and environmental crisis. The hydrogen evolution reaction (HER), capable of producing high-purity hydrogen rapidly in electrocatalytic water splitting, has received much attention. Abundant research about HER has been done, focusing on advanced electrocatalyst design with high efficiency and robust stability. As potential HER catalysts, metal nanoclusters (MNCs) have been studied extensively. They are composed of several to a hundred metal atoms, with sizes being comparable to the Fermi wavelength of electrons, that is, < 2.0 nm. Different from metal atoms/nanoparticles, they exhibit unique catalytic properties due to their quantum size effect and low-coordination environment. In this review, the activity-enhancing approaches of MNCs applied in HER electrocatalysis are mainly summarized. Furthermore, recent progress in MNCs classified with different stabilization strategies, that is, the freestanding MNCs, MNCs with organic, metal and carbon supports, are introduced. Finally, the current challenges and deficiencies of these MNCs for HER are prospected.

Surface-Orientation Elimination of Vapor-Deposited PbI2 Flakes for Efficient Perovskite Synthesis on Curved Solar Cells.

Vapor deposition of perovskite solar cells (PSCs) has attracted considerable interest for its dry processing characteristics. However, a two-step sequential vapor deposition method suffers from ineffective conversion of PbI2 to perovskite with reasons still unclear. In this report, we carefully investigated the crystallization orientation of PbI2 films deposited by physical vapor deposition via synchrotron grazing-incidence wide-angle X-ray scattering (GIWAXS) and observed an asymmetric scattering pattern with respect to the qz-axis. The observed oriented morphology and texture hinder the diffusion of MAI molecules in the PbI2 films synthesized by vapor deposition, resulting in over 15% PbI2 remaining at the buried interface after reaction with MAI vapor. As a result, the MAPbI3 synthesized in this way was also highly oriented, especially in the surface layers. Surface fumigation (SF) step was introduced to decrease the orientational anisotropy of PbI2, which successfully breaks the diffusion barriers of MAI molecules by forming a complex layer on the PbI2 surface with polar solvent vapors, like dimethyl sulfoxide or 1,3-dimethyl-2-imidazolidinone. We infer that the SF treatment changes the vapor-solid reaction mechanism from reaction-crystallization to dissolution-recrystallization, which largely promotes the conversion of PbI2 to perovskite. Defects were reduced in perovskite synthesized in this way, and a p-i-n device with 19.56% efficiency was fabricated, which is among the highest efficiencies reported for sequential-vapor-deposited PSCs. Notably, this method enables the fabrication of conformal perovskite layers on uneven substrates. An exemplary PSC showing efficiency of 8.93% was fabricated on a precurved substrate. We believe that the method is applicable to the fabrication of tandem or curved PSCs that are compatible with wearable or building/autocar-integrated photovoltaics in the future.

Precursor Engineering of Vapor-Exchange Processes for 20%-Efficient 1 cm2 Inverted-Structure Perovskite Solar Cells.

Due to mass diffusion issues, it is challenging to prepare black-phase thick formamidinium-based perovskite (FAPbI3) films via vapor approaches. Precursor engineering is employed here to overcome the dilemma of thorough reaction and black-phase stabilization of FAPbI3 in a sequential vapor approach. For the first time, FAPbBr3 was used as an additive in the precursor to promote the formation of FAPbI3 perovskite. To balance off the increased crystallization degree of precursor films due to the addition of FAPbBr3, CsI dissolved in dimethyl sulfoxide (DMSO) was further added. It is indicated that the simultaneous incorporation of FAPbBr3 and CsI-DMSO successfully accelerated the formation rate of perovskite and inhibited the formation of FAPbI3 yellow phase. The power conversion efficiency of the as-prepared devices of different areas (0.1125 or 1 cm2) reached 20%, the first report of large-area 20%-efficiency PSCs based on a vapor approach, highlighting its applicability to large-area manufacture in the future. Furthermore, when blade coating is used in preparing the precursor film, the efficiency reached 19%. When the precursor film was prepared by dip coating, we could prepare conformal FAPbI3 coatings on carbon fibers, suggesting possible future applications in fabricating wearable PSCs.

Understanding the oriented-attachment growth of nanocrystals from an energy point of view: a review.

Since Penn et al. first discovered the oriented attachment growth of crystals, the oriented attachment mechanism has now become a major research focus in the crystal field, and extensive efforts have been carried out over the past decade to systematically investigate the growth mechanism and the statistical kinetic models. However, most of the work mainly focuses on the experimental results on the oriented attachment growth. In contrast to the previous reviews, our review provides an overview of the recent theoretical advances in oriented attachment kinetics combined with experimental evidences. After a brief introduction to the van der Waals interaction and Coulombic interaction in a colloidal system, the correlation between the kinetic models of oriented attachment growth and the interactions is then our focus. The impact of in situ experimental observation techniques on the study of oriented attachment growth is examined with insightful examples. In addition, the advances in theoretical simulations mainly investigating the thermodynamic origin of these interactions at the atomic level are reviewed. This review seeks to understand the oriented attachment crystal growth from a kinetic point of view and provide a quantitative methodology to rationally design an oriented attachment system with pre-evaluated crystal growth parameters.