Travel before, during and after the COVID-19 pandemic: Exploring factors in essential travel using empirical data.

The COVID-19 pandemic has a significant impact on daily life, leading to quarantines and essential travel restrictions worldwide in an effort to curb the virus's spread. Despite the potential importance of essential travel, research on changes in travel patterns during the pandemic has been limited, and the concept of essential travel has not been fully explored. This paper aims to address this gap by using GPS data from taxis in Xi'an City between January and April 2020 to investigate differences in travel patterns across three periods pre, during, and post the pandemic. Spatial statistical models are used to examine the major supply and demand-oriented factors that affect spatial travel patterns in different periods, and essential and nonessential socioeconomic resources are defined based on types of services. Results indicate that the spatial distribution of travel demand was highly correlated with the location of socioeconomic resources and opportunities, regardless of the period. During the "Emergency Response" period, essential travel was found to be highly associated with facilities and businesses providing essential resources and opportunities, such as essential food provider, general hospital and daily grocery supplies. The findings suggest that local authorities may better identify essential travel destinations by referencing the empirical results, strengthening public transit connections to these locations, and ultimately promoting traffic fairness in the post-pandemic era.

Parallel Planar Heterojunction Strategy Enables Sb2 S3 Solar Cells with Efficiency Exceeding 8 .

Solution-processed solar cells based on inorganic heterojunctions provide a potential approach to the efficient, stable and low-cost solar cells required for the terrestrial generation of photovoltaic energy. Antimony trisulfide (Sb2 S3 ) is a promising photovoltaic absorber. Here, an easily solution-processed parallel planar heterojunction (PPHJ) strategy and related principle are developed to prepare efficient multiple planar heterojunction (PHJ) solar cells, and the PPHJ strategy boosts the efficiency of solution-processed Sb2 S3 solar cells up to 8.32 % that is the highest amongst Sb2 S3 devices. The Sb2 S3 -based PPHJ device consists of two kinds of conventional planar heterojunction (PHJ) subcells in a parallel connection: Sb2 S3 -based PHJ subcells dominating the absorption and charge generation and CH3 NH3 PbI3 -based PHJ subcells governing the electron transport towards collection electrode, but it belongs to an Sb2 S3 device in nature. The resulting PPHJ device combines together the distinctive structural features of Sb2 S3 absorbing layer as a main absorber and the duplexity of well-crystallized/oriented CH3 NH3 PbI3 layer in charge transportation as an additional absorber, while the presence of perovskite does not affect device stability. The PPHJ strategy maintains the facile preparation by the conventional sequential depositions of multiple layers, but eliminates the normal complexity in both tandem and parallel tandem PHJ systems.

Dimension-Confined Growth of a Crack-Free PbS Microplate Array for Infrared Image Sensing.

Epitaxy of semiconductors is a necessary step toward the development of electronic devices such as lasers, detectors, transistors, and solar cells. However, the lattice ordering of semiconductor functional films is inevitably disrupted by excessive concentrated stress due to the mismatch of the thermal expansion coefficient. Herein, combined with the first-principles calculation, we find that a rigid film/substrate bilayer heterostructure with a large thermal expansion mismatch upon cooling to room temperature from growth is free of surface cracks when the rigid film exhibits a dimension smaller than the critical condition for the breaking energy. The principle has been verified in a PbS/SrTiO3 bilayer system that is crack free on PbS single-crystalline microplate arrays through the designing of a dimension-confined growth (DCG) method. Interestingly, this crack-free, large-scale PbS microplate array exhibits exceptional uniformity in morphology, dimensions, thickness, and photodetection properties, enabling a broad-band infrared image sensing. This work provides a new perspective to design materials and arrays that demand smooth and continuous surfaces, which are not limited only to semiconductor electronics but also include mechanical structures, optical materials, biomedical materials, and others.

Solution-Processed All-inorganic Planar Heterojunction Solar Cells by Employing In Situ Grown Interfacial Layer with Dual Functions: Complementary Absorption and Selective Extraction of Photogenerated Holes.

Photovoltaic conversion of renewable solar energy into electricity for sustainable energy production requires efficient, stable, and low-cost solar cells. Developing solution-processed all-inorganic solar cells is a practical scenario in virtue of the high charge mobility and good stability of inorganic semiconductors. Here, for the first time, we present a solution-processed all-inorganic planar heterojunction solar cell based on the nanoparticle film of copper indium sulfide (CuInS2) by using an antimony trisulfide (Sb2S3) nanoparticle film as an interfacial layer between the CuInS2 photon-harvesting layer and cathode. All of the component layers in the solar cell are in a superstrate architecture and sequentially in situ grown on a transparent conducting glass acting as anode by solution-processing methods. The dependences of device performance on the thickness of Sb2S3 film and the reduction of hole-trapping centers in the Sb2S3 film by thioacetamide treatment are investigated. The optimized all-inorganic device exhibits the best power conversion efficiency of 4.85% under AM 1.5G illumination and an excellent thermal stability. It is found that the Sb2S3 interfacial layer sandwiched between the CuInS2 photon-harvesting layer and counter-electrode has dual functions, that is, to provide complementary absorption after CuInS2 attenuation and to act as an effective hole-transporting layer to selectively extract photogenerated holes for effective charge collection efficiency.

Improving Performance of Nonfullerene Organic Solar Cells over 13% by Employing Silver Nanowires-Doped PEDOT:PSS Composite Interface.

Ag nanowires (NWs)/PEDOT:PSS composite was prepared by a facile solution-processing method and employed as anode interface in nonfullerene organic solar cells (OSCs). In the presence of a Ag NWs (5%, v/v%)/PEDOT:PSS interfacial layer, a high-power conversion efficiency up to 13.53% was achieved based on a PBDB-T-2Cl:IT-4F photoactive layer system, much higher than the efficiency of the controlled counterpart device with pristine PEDOT:PSS as anode modifier. Simultaneous enhancements in short-circuit current and fill factor were observed, in comparison to the case of the pristine PEDOT:PSS interface, due to the improved electrical conductivity of Ag NWs/PEDOT:PSS composites accompanied by the increased work function for a better matching with the indium tin oxide counter electrode, which facilitated increased charge transfer and reduced charge recombination at the anode/photoactive interface for improved device performance. The results clearly revealed that the Ag NWs/PEDOT:PSS composite interface is beneficial to improve the charge extraction and favor the realization of highly efficient nonfullerene OSCs.

Growth of Compact CH3NH3PbI3 Thin Films Governed by the Crystallization in PbI2 Matrix for Efficient Planar Perovskite Solar Cells.

As a convenient preparation technique, a two-step method, which is normally done by spin-coating CH3NH3I onto PbI2 film followed by a thermal annealing, is generally used to prepare solution-processed CH3NH3PbI3 films for planar perovskite solar cells. Here, we prepare the compact CH3NH3PbI3 thin films by the two-step method at a low temperature (<80 °C) and investigate the effects of PbI2 crystallization on the structure-property correlation in the CH3NH3PbI3 films. It is found that the importance of the crystallization in PbI2 matrix lies in governing the transition from the (001) plane of trigonal PbI2 to the (002) plane of tetragonal CH3NH3PbI3 in the rapid reaction process for atoms to coordinate into perovskite during spin-coating, which actually determines the morphology and the type of vacancy defects in resulting perovskite; a better crystallized PbI2 film has a much stronger ability to react with CH3NH3I solution and produces larger CH3NH3PbI3 grains with a higher crystallinity. The CH3NH3PbI3/TiO2 planar solar cell derived from a better crystallized PbI2 film exhibits significantly improved performance and stability as the result of the higher crystallinity inside the perovskite film. Moreover, it is demonstrated that the crystalline PbI2 film matrix subjected to the annealing after a slow heating process prior to contacting CH3NH3I solution is more effective for CH3NH3PbI3 formation than that with a direct annealing history. The results in this paper provide a guide for preparing high-quality CH3NH3PbI3 thin films for efficient perovskite solar cells and CH3NH3PbI3 interfacial films over the layers susceptible to temperature.