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There have been huge achievements of all‐perovskite tandem solar cells, which recently realized the highest power conversion efficiency of 24.8%. However, the complex device structure and complicated manufacture processes severely restrict the further development of all‐perovskite tandem solar cells. In this work, we successfully fabricated high‐efficiency hole transport material‐free (HTM‐free) Sn−Pb alloyed narrow bandgap perovskite solar cells (PSCs) by introducing guanidinium thiocyanate (GASCN) and hydroiodic acid (HI) into the perovskite precursor solution. GASCN and HI play a positive synergy effect during perovskite crystallization process resulting in larger grain size, fewer surface defects, and lower trap density to suppress the Sn2+ oxidation degradation. Furthermore, they could effectively adjust the energy level of perovskite materials, reduce the energy level difference between perovskite and ITO resulting in more efficiently transport of free hole charge carriers. As a result, with adding GASCN and HI, the achieved highest power conversion efficiency of HTM‐free devices increased from 12.58% to 17.85%, which is one of the highest PCEs among all values reported to date for the HTM‐free narrow‐bandgap (1.2–1.4 eV) Sn−Pb binary PSCs. Moreover, the optimized device shows improved environmental stability. Our additive strategy manifests a remarkable step towards the facile, cost‐efficient fabrication of HTM‐free perovskite‐based tandem solar cells with both high efficiency and simple fabrication process. [ABSTRACT FROM AUTHOR]

A H2SO4-Ti3C2Tx ion-gel is in situ fabricated to prevent the restacking of Ti3C2Tx for high-rate micro-supercapacitors. The ion-gel pillared by an electrolyte possesses an enlarged interlayer spacing facilitating ion transport. Furthermore, a bilayer structure is designed with dry Ti3C2Tx for fast electron conduction. The bilayer Ti3C2Tx film shows improved capacitance from 49% to 73% of the initial capacitance at a high scan rate of 200 mV s−1, along with excellent cycle stability. This study opens up a concise and efficient way for high-performance micro-supercapacitors. [ABSTRACT FROM AUTHOR]

Iron-based constructed wetlands (ICWs) displayed great potential in deep nitrogen elimination for low-polluted wastewater. However, the unsatisfactory denitrification performance caused by the limited solubility and sluggish activity of iron substrates needs to be improved in an eco-effective manner. To fill this gap, the bioavailability of iron substrates (iron scraps) affected by wetland biomass-derived carbon materials with potential conductivity were explored. Results indicated that the cumulative removal of TN in biochar-added ICW (BC-ICW) and activated carbon-added ICW (AC-ICW) increased by 29.04 % and 22.96 %, respectively. The carbon matrix of AC played the geo-conductor role to facilitate the rapid release of iron ions, as indicated by the higher TN removal efficiency of AC-ICW (45.36 ± 1.45 %) at the early stage, while the reduced conductivity of AC negatively impacted the nitrogen removal. BC-ICW exhibited intensified denitrification potential, with higher TN removal capacity (52.08 ± 3.04 %) and effluent Fe 2+ concentration. Electroactive bacteria (EB) (Geobacter, Desulfovibrio, Shewanella, etc.) associated with extracellular electron transfer were enriched in BC-ICW, as well as the expanded niches breadth and improved microbial community diversity. The electron-shuttling effect of BC was mainly attributed to its oxygenated functional groups (quinone/phenolic moieties), which supported the electron transfer from EB to extracellular iron oxides, as evidenced by the increased Fe(III)(hydro)oxides bioavailability. Besides, biochar concurrently up-regulated the gene expression of electron transport chains/mediators and denitrification reductases, suggesting that BC boosted the active iron cycle and iron-mediated autotrophic denitrification in ICWs by accelerating intracellular and extracellular electron transfer. This work explored the electron transfer behavior of biomass-derived carbon materials coupled with ICWs to enhance denitrification, providing insights into the sustainable application of biomass derived carbon-assisted ICWs in tertiary treatment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2025 Elsevier Ltd. All rights reserved.)