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All‐inorganic cesium lead triiodide perovskites (CsPbI3) have attracted increasing attention due to their good thermal stability, remarkable optoelectronic properties, and adaptability in tandem solar cells. However, N2‐filled glovebox is generally required to strictly control the humidity during film fabrication due to the moisture‐induced black‐to‐yellow phase transition, which remains a great hinderance for further commercialization. Herein, we report an effective approach via incorporating multifunctional ethacridine lactate (EAL) to mitigate moisture invasion and enable the fabrication of efficient inverted (p‐i‐n) CsPbI3 perovskite solar cells (PSCs) under ambient condition. It is revealed that the lactate anions accelerate the crystallization of CsPbI3, shortening the exposure time to moisture during film fabrication. Meanwhile, the conjugated backbone and multiple functional groups in the ethacridine cations can interact with I− and Pb2+ to reduce the undesired defects, stabilize the perovskite structure and facilitate the charge transport in the film. Moreover, EAL incorporation also leads to better energy alignment, thus favoring charge extraction at both upper and bottom interfaces. Consequently, the device efficiency and stability are enormously enhanced, with the champion efficiency reaching 21.08 %. This even surpasses the highest value reported for the devices fabricated in glovebox, representing a record efficiency of inverted all‐inorganic PSCs. [ABSTRACT FROM AUTHOR]

Tin perovskite solar cells (PSCs) are considered promising candidates to promote lead‐free perovskite photovoltaics. However, their power conversion efficiency (PCE) is limited by the easy oxidation of Sn2+ and low quality of tin perovskite film. Herein, an ultra‐thin 1‐carboxymethyl‐3‐methylimidazolium chloride (ImAcCl) layer is used to modify the buried interface in tin PSCs, which can induce multifunctional improvements and remarkably enhance the PCE. The carboxylate group (CO) and the hydrogen bond donor (NH) in ImAcCl can interact with tin perovskites, thus significantly suppressing the oxidation of Sn2+ and reducing the trap density in perovskite films. The interfacial roughness is reduced, which contributes to a high‐quality tin perovskite film with increased crystallinity and compactness. In addition, the buried interface modification can modulate the crystal dimensionality, favoring the formation of large bulk‐like crystals instead of low‐dimensional ones in tin perovskite films. Therefore, the charge carrier transport is effectively promoted and the charge carrier recombination is suppressed. Eventually, tin PSCs show a remarkably enhanced PCE from 10.12% to 12.08%. This work highlights the importance of buried interface engineering and provides an effective way to realize efficient tin PSCs. [ABSTRACT FROM AUTHOR]

A series of RbxK2−xCaPO4F:Eu2+ phosphors are synthesized using a high‐temperature solid‐phase method. An increase in the Rb+ concentration leads to the Eu2+‐excited phosphor emission spectra being shifted from red to cyan. Interestingly, the excitation spectrum does not exhibit any variations, which indicates the possibility of mixing the red (Rb0.2K1.8CaPO4F:Eu2+) and cyan (Rb2CaPO4F:Eu2+) phosphors for plant growth. This luminescence tuning is attributed to the substitution of K+ with Rb+, which produces an inferior crystal‐field splitting that increases the energy at the lowest 5d level, and enhances the rigidity of the crystal structure, which results in a gradual decrease in the Stokes shift and a consequent blue shift in the emission spectrum. Time‐resolved photoluminescence emission spectroscopy further confirms the occurrence of broadband emission owing to the occupation of multiple sites by Eu2+. Light‐emitting devices appropriate for plant growth are fabricated by mixing the two phosphors with a 380‐nm UV chip, and a light‐conversion film is prepared using the red phosphor and PDMS glue. The Chlorella‐based plant growth experiment reveals that the growth rate of Chlorella is 12.2% higher than that of the blank group, indicating the favorable effect of the light‐conversion film on plant growth. [ABSTRACT FROM AUTHOR]

The auxiliary light equipment for plant growth requires phosphor-converted light-emitting-diodes (pc-LEDs) with high luminous efficiency and a stable structure, and the properties of phosphors highly determine the performance of the pc-LEDs. This work reports a deep-red emitting phosphor with an ultra-wide response range which is regarded as CaMgAl10O17:Mn4+. The absorption range spans the ultraviolet, near-ultraviolet, blue, and green light regions from 250 to 550 nm. Under the excitation of the best excitation position at 343 nm, deep-red light at 654 nm is emitted, and the quantum efficiency is as high as 86.7%. The luminous efficiency of the two pc-LED devices prepared based on CaMgAl10O17:Mn4+ with 395 and 460 nm chips reached 54.3 and 59.6 lm W−1, respectively. The spectra of the two pc-LEDs exhibit high resemblance to the absorption spectra of chlorophyll A and B in plant growth photosynthesis. These indicate that the CaMgAl10O17:Mn4+ phosphor can be an excellent candidate for plant growth LED light. [ABSTRACT FROM AUTHOR]

The auxiliary light equipment for plant growth requires phosphor-converted light-emitting-diodes (pc-LEDs) with high luminous efficiency and a stable structure, and the properties of phosphors highly determine the performance of the pc-LEDs. This work reports a deep-red emitting phosphor with an ultra-wide response range which is regarded as CaMgAl 10 O 17 :Mn 4+ . The absorption range spans the ultraviolet, near-ultraviolet, blue, and green light regions from 250 to 550 nm. Under the excitation of the best excitation position at 343 nm, deep-red light at 654 nm is emitted, and the quantum efficiency is as high as 86.7%. The luminous efficiency of the two pc-LED devices prepared based on CaMgAl 10 O 17 :Mn 4+ with 395 and 460 nm chips reached 54.3 and 59.6 lm W -1 , respectively. The spectra of the two pc-LEDs exhibit high resemblance to the absorption spectra of chlorophyll A and B in plant growth photosynthesis. These indicate that the CaMgAl 10 O 17 :Mn 4+ phosphor can be an excellent candidate for plant growth LED light.