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Carrier transport layers have been recognized as a key factor to determine the performance of perovskite solar cells (PSCs) by dominating the charge carrier extraction, transport and recombination process. Metal oxides have been widely used as electron transport layers (ETLs) in PSCs for high performance and stability, of which TiO2 and SnO2 are the most popular choices. However, the large-scale implementation of TiO2 and SnO2 ETLs is hindered by their own deficiencies, such as low electron mobility, poor stability against UV light and surface defects. Therefore, binary and ternary metal oxide alternatives have been widely investigated recently. Here, we review the recent advances of these metal oxide ETLs in PSCs with a special focus on the nanostructuring, elemental doping, surface modification, and multi-layer ETLs and large-scale fabrication of these ETLs. Furthermore, the state-of-the-art progress towards high-efficiency and stable PSCs using these novel ETLs is summarized and future perspectives are discussed. [ABSTRACT FROM AUTHOR]

Metal halide perovskite materials have drawn worldwide attention for application in a variety of optoelectronic devices, especially in the emerging photovoltaic devices. In recent years, remarkable progress has been achieved in the device performance and stability. The optoelectronic properties of metal halide perovskites can be further tuned by ion doping. Herein, a comprehensive review of the incorporation of alkali metal ions (Li+, Na+, K+ and Rb+) in emerging perovskite solar cells for a longer carrier lifetime, lower interfacial defect density, faster charge transfer, no hysteresis, higher stability and higher power conversion efficiency is presented. The detailed mechanism behind these beneficial effects has been discussed in terms of electronic properties, film morphology, energy level alignment, carrier recombination dynamics and stability. On the basis of these latest advances and breakthroughs in alkali ion doped perovskite thin films, future research directions and prospects are also discussed, which include further understanding of the underlying photophysical mechanism and extension to other optoelectronic devices where a longer carrier lifetime and lower trap density are needed. [ABSTRACT FROM AUTHOR]

As a carbon-neutral alternative to the Haber–Bosch process, electrochemical N2 reduction enables environment-friendly NH3 synthesis under ambient conditions but needs active electrocatalysts for the N2 reduction reaction (NRR). In this communication, we report on the first experimental demonstration that non-metal boron phosphide (BP) nanoparticles can be used as a high-efficiency catalyst for the ambient electrohydrogenation of N2 to NH3 with excellent selectivity. In 0.1 M HCl, this catalyst offers a high NH3 yield of 26.42 μg h−1 mgcat.−1 and a high faradaic efficiency of 12.7% at −0.60 V vs. the reversible hydrogen electrode, much superior to those of reported B catalysts. Such an enhancement is attributed to the fact that P in BP further weakens the N≡N bond while simultaneously strengthening the B–N bond and favors the exposure of more active sites for the NRR catalysis, which is supported by density functional theory calculations. [ABSTRACT FROM AUTHOR]