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Supercapacitors are widely recognized as a favorable option for energy storage due to their higher power density compared to batteries, despite their lower energy density. However, to meet the growing demand for increased energy capacity, it is crucial to explore innovative materials that can enhance energy storage efficiency. Recent research has focused on investigating various electrode materials for use in supercapacitors, with particular attention given to MXenes. MXenes exhibit immense potential for energy storage due to their unique characteristics, including a 2D van der Waals layered structure, small band gaps, hydrophilic surface, excellent electrical conductivity, high specific surface area, and active redox sites on the surface facilitated by transition metals. These attributes collectively contribute to their promising stability, energy and power density, and overall lifespan. This comprehensive review explores a diverse array of topics pertaining to the latest 2D MXene-based supercapacitor electrodes. It encompasses discussions on different synthesis methods, electrode structures, the underlying working mechanisms, and the impact of electrolytes on supercapacitor performance. Additionally, a concise overview of various types of MXene materials is presented, ranging from titanium-based MXenes to niobium-based MXenes, vanadium-based MXenes, molybdenum-based MXenes, and tantalum-based MXenes. Furthermore, this review focuses on electronic structure engineering strategies such as heterostructures based on MXenes, heteroatom-doping based on MXenes, polymer based MXenes, and ternary composites based on MXenes, all of which contribute to improving the electrochemical performance of supercapacitors. The review thoroughly examines the advantages and disadvantages of MXene-based supercapacitor electrodes, offering a comprehensive understanding of their strengths and limitations. Additionally, it discusses the structural stability of MXene-based electrodes after electrochemical testing, as well as their applications in daily human life, particularly focusing on the uses of MXene-based flexible wearable energy storage for real-world applications. In the end, the challenges and prospects of MXenes in supercapacitors are discussed. 

Structurally well-defined polymer-grafted nanoparticle hybrids are highly sought after for a variety of applications, such as antifouling, mechanical reinforcement, separations, and sensing. Herein, we report the synthesis of poly(methyl methacrylate) grafted- and poly(styrene) grafted-BaTiO3 nanoparticles using activator regeneration via electron transfer (ARGET ATRP) with a sacrificial initiator, atom transfer radical polymerization (normal ATRP), and ATRP with sacrificial initiator, to understand the role of the polymerization procedure in influencing the structure of nanoparticle hybrids. Irrespective of the polymerization procedure adopted for the synthesis of nanoparticle hybrids, we noticed PS grafted on the nanoparticles showed moderation in molecular weight and graft density (ranging from 30,400 to 83,900 g/mol and 0.122 to 0.067 chain/nm2) compared to PMMA-grafted nanoparticles (ranging from 44,620 to 230,000 g/mol and 0.071 to 0.015 chain/nm2). Reducing the polymerization time during ATRP has a significant impact on the molecular weight of polymer brushes grafted on the nanoparticles. PMMA-grafted nanoparticles synthesized using ATRP had lower graft density and considerably higher molecular weight compared to PS-grafted nanoparticles. However, the addition of a sacrificial initiator during ATRP resulted in moderation of the molecular weight and graft density of PMMA-grafted nanoparticles. The use of a sacrificial initiator along with ARGET offered the best control in achieving lower molecular weight and narrow dispersity for both PS (37,870 g/mol and PDI of 1.259) and PMMA (44,620 g/mol and PDI of 1.263) nanoparticle hybrid systems. 

Abstract Dimethylammonium lead iodide (DMAPbI_x) has the potential to address the phase stability issue of inorganic perovskite solar cells (PSCs). In this study, the crystallinity, phase structure, defect states, and crystal growth habits of DMAPbI_xare controlled by adjusting thexvalue during synthesis, where N,N‐dimethylacetamide (DMAC) is used as the solvent to regulate perovskite film growth. Furthermore, large‐area CsPbI_2.85Br_0.15perovskite films with preferred oriented growth are achieved using the optimizedxvalue in DMAPbI_xthrough the slot‐die coating method. The inorganic PSCs, with a n‐i‐p structure and the active area of 0.04 cm², achieve a champion power conversion efficiency (PCE) of 19.82%, with an open‐circuit voltage (V_oc) of 1.16 V based on perovskite films formed by slot‐die coating. This work provides important insights into the DMAPbI_x‐based method for fabricating high‐quality inorganic perovskite films, and paves the way for large‐area inorganic PSCs fabrication for practical applications.