Regional differences and convergence of green innovation efficiency in China.

Green innovation facilitates high-quality economic development and ecological environmental protection. Herein, the minimum distance to strong efficient frontier (MinDS) model was used to measure green innovation efficiencies (GIEs) of 30 Chinese provinces over a period of 21 years (2000-2020). Gini coefficient decomposition and kernel density estimation methods were used to analyze the regional differences of GIE. Spatial correlation was estimated to analyze spatial-spillover effects and spatial convergence of the GIE. China's GIE has shown an increasing trend with significant spatial differences in GIE among provinces. Regional differences and transvariation intensity are the primary sources of spatial differences in GIE. Regional differences in GIE have decreased, except for eastern regions. The results of spatial convergence estimation suggest spatial absolute and conditional convergence in all regions. Therefore, for the GIE improvement in China, the effects of economic level, industrial structure, and environmental regulations must be considered.

Inhibition of Phase Segregation in Cesium Lead Mixed-Halide Perovskites by B-Site Doping.

The emergence of all-inorganic halide perovskites has shown great potential in photovoltaic and optoelectronic devices. However, the photo-induced phase segregation in lead mixed-halide perovskites has severely limited their application. Herein, by real-time monitoring the photoluminescence (PL) spectra of metal mixed-halide perovskites under light irradiation, we found that the photo-induced phase transition can be significantly inhibited by B-site doping. For pristine mixed-halide perovskites, an intermediate phase of CsPbBrxI3-x can only be stabilized under low excitation power. After introducing Sn2+ ions, such intermediate phase can be stabilized in nitrogen atmosphere under high excitation power and phase segregation can be started after the exposure in oxygen due to oxidization of Sn2+. Replacing Sn2+ by Mn2+ can further improve the intermediate phase's tolerance to oxygen proving that B-site doping in perovskites structure by Sn2+ or Mn2+ could effectively minimize the light-induced phase segregation and promote them to serve as promising candidates in photovoltaic and light-emitting devices.

Controlled growth and ion intercalation mechanism of monocrystalline niobium pentoxide nanotubes for advanced rechargeable aluminum-ion batteries.

Rechargeable aluminum-ion batteries (RAIBs) have attracted increasing attention owing to their high theoretical volumetric capacity, high resource abundance, and good safety performance. However, the existing RAIB systems usually exhibit relatively low specific capacities limited by the cathode materials. In this study, we developed a one-step chemical vapor deposition method to prepare single-crystal orthogonal Nb2O5 nanotubes for serving as high-performance electrode materials for RAIBs, showing a high reversible capability of 556 mA h g-1 at 25 mA g-1 and good thermal endurability at elevated temperatures (50 °C). A combination of a series of detailed ex situ structural characterization studies verified the reversible intercalation/deintercalation of chloroaluminate anions (AlCl4-) into/from the (001) planes of monocrystalline Nb2O5 nanotubes. It also revealed that the nanoarchitecture of Nb2O5 nanotubes with thin tube walls, hollow inner space and a short ion transport distance is conducive to the rapid kinetics of the insertion/extraction process. This work provides a promising route to design high-performance electrode materials based on transition metal compounds for RAIBs via the rational modulation of their structure and morphology.

Determination of complex optical constants and photovoltaic device design of all-inorganic CsPbBr3 perovskite thin films.

All-inorganic perovskites exhibit interesting properties and unprecedented stability compared to organic-inorganic hybrid lead halide perovskites. This work focuses on depositing and characterizing cesium lead bromide (CsPbBr3) thin films and determining their complex optical constants, which is a key requirement for photovoltaic device design. CsPbBr3 thin films are synthesized via the solution method followed by a hot-embossing step to reduce surface roughness. Variable angle spectroscopic ellipsometry measurements are then conducted at three angles (45°, 55°, and 65°) to obtain the ellipsometric parameters psi (Ψ) and delta (Δ). For the present model, bulk planar CsPbBr3 layer is described by a one-dimensional graded index model combined with the mixture of one Tauc-Lorentz oscillator and two Gaussian oscillators, while an effective medium approximation with 50% air void is adopted to describe surface roughness layer. The experimental complex optical constants are finally determined in the wavelength range of 300 to 1100 nm. Furthermore, as a design example demonstration, the simulations of single-junction CsPbBr3 solar cells are conducted via the finite-difference time-domain method to investigate the properties of light absorption and photocurrent density.

Nitrogen-Doped Carbon Nanotube Forests Planted on Cobalt Nanoflowers as Polysulfide Mediator for Ultralow Self-Discharge and High Areal-Capacity Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries with high theoretical energy density have caught enormous attention for electrochemical power source applications. However, the development of Li-S batteries is hindered by the electrochemical performance decay that resulted from low electrical conductivity of sulfur and serious shuttling effect of intermediate polysulfides. Moreover, the areal capacity is usually restricted by the low areal sulfur loadings (1.0-3.0 mg cm-2). When the areal sulfur loading increases to a practically accepted level above 3.0-5.0 mg cm-2, the areal capacity and cycling life tend to become inferior. Herein, we report an effective polysulfide mediator composed of nitrogen-doped carbon nanotube (N-CNT) forest planted on cobalt nanoflowers (N-CNTs/Co-NFs). The abundant pores in N-CNTs/Co-NFs can allow a high sulfur content (78 wt %) and block the dissolution/diffusion of polysulfides via physical confinement, and the Co nanoparticles and nitrogen heteroatoms (4.3 at. %) can enhance the polysulfide retention via strong chemisorption capability. Moreover, the planted N-CNT forest on N-CNTs/Co-NFs can enable fast electron transfer and electrolyte penetration. Benefiting from the above merits, the sulfur-filled N-CNTs/Co-NFs (S/N-CNTs/Co-NFs) cathodes with high areal sulfur loadings exhibit low self-discharge rate, high areal capacity, and stable cycling performance.

Interface Engineering of Anchored Ultrathin TiO2/MoS2 Heterolayers for Highly-Efficient Electrochemical Hydrogen Production.

An efficient self-standing hydrogen evolution electrode was prepared by in situ growth of stacked ultrathin TiO2/MoS2 heterolayers on carbon paper (CP@TiO2@MoS2). Owing to the high overall conductivity, large electrochemical surface area and abundant active sites, this novel electrode exhibits an excellent performance for hydrogen evolution reaction (HER). Remarkably, the composite electrode shows a low Tafel slope of 41.7 mV/dec, and an ultrahigh cathodic current density of 550 mA/cm2 at a very low overpotential of 0.25 V. This work presents a new universal strategy for the construction of effective, durable, scalable, and inexpensive electrodes that can be extended to other electrocatalytic systems.

Porous-Shell Vanadium Nitride Nanobubbles with Ultrahigh Areal Sulfur Loading for High-Capacity and Long-Life Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries hold great promise for the applications of high energy density storage. However, the performances of Li-S batteries are restricted by the low electrical conductivity of sulfur and shuttle effect of intermediate polysulfides. Moreover, the areal loading weights of sulfur in previous studies are usually low (around 1-3 mg cm-2) and thus cannot fulfill the requirement for practical deployment. Herein, we report that porous-shell vanadium nitride nanobubbles (VN-NBs) can serve as an efficient sulfur host in Li-S batteries, exhibiting remarkable electrochemical performances even with ultrahigh areal sulfur loading weights (5.4-6.8 mg cm-2). The large inner space of VN-NBs can afford a high sulfur content and accommodate the volume expansion, and the high electrical conductivity of VN-NBs ensures the effective utilization and fast redox kinetics of polysulfides. Moreover, VN-NBs present strong chemical affinity/adsorption with polysulfides and thus can efficiently suppress the shuttle effect via both capillary confinement and chemical binding, and promote the fast conversion of polysulfides. Benefiting from the above merits, the Li-S batteries based on sulfur-filled VN-NBs cathodes with 5.4 mg cm-2 sulfur exhibit impressively high areal/specific capacity (5.81 mAh cm-2), superior rate capability (632 mAh g-1 at 5.0 C), and long cycling stability.

CsPb0.9Sn0.1IBr2 Based All-Inorganic Perovskite Solar Cells with Exceptional Efficiency and Stability.

The emergence of perovskite solar cells (PSCs) has generated enormous interest in the photovoltaic research community. Recently, cesium metal halides (CsMX3, M = Pb or Sn; X = I, Br, Cl or mixed halides) as a class of inorganic perovskites showed great promise for PSCs and other optoelectronic devices. However, CsMX3-based PSCs usually exhibit lower power conversion efficiencies (PCEs) than organic-inorganic hybrid PSCs, due to the unfavorable band gaps. Herein, a novel mixed-Pb/Sn mixed-halide inorganic perovskite, CsPb0.9Sn0.1IBr2, with a suitable band gap of 1.79 eV and an appropriate level of valence band maximum, was prepared in ambient atmosphere without a glovebox. After thoroughly eliminating labile organic components and noble metals, the all-inorganic PSCs based on CsPb0.9Sn0.1IBr2 and carbon counter electrodes exhibit a high open-circuit voltage of 1.26 V and a remarkable PCE up to 11.33%, which is record-breaking among the existing CsMX3-based PSCs. Moreover, the all-inorganic PSCs show good long-term stability and improved endurance against heat and moisture. This study indicates a feasible way to design inorganic halide perovskites through energy-band engineering for the construction of high-performance all-inorganic PSCs.

Solution synthesis and phase control of inorganic perovskites for high-performance optoelectronic devices.

An efficient method to synthesize well-crystallized inorganic cesium lead halide perovskites (CsPbX3, X = I or Br) with high yield and high reproducibility was proposed. Notably, the as-prepared CsPbI3 in the yellow orthorhombic phase (y-CsPbI3) can be easily converted to the black cubic perovskite phase CsPbI3 (b-CsPbI3) after thermal annealing. Furthermore, two-terminal photodetectors and all-inorganic perovskite solar cells based on b-CsPbI3 were fabricated, exhibiting high performances.