A family of 2D transition metal carbides and nitrides known as MXenes has received increasing attention since the discovery of Ti₃C₂ in 2011. To date, about 30 different MXenes with well‐defined structures and properties have been synthesized, and many more are theoretically predicted to exist. Due to the numerous assets including excellent mechanical properties, metallic conductivity, unique in‐plane anisotropic structure, tunable band gap, and so on, MXenes rapidly positioned themselves at the forefront of the 2D materials world and have found numerous promising applications. Particular interest is devoted to applications in electrochemical energy storage, whereby 2D MXenes work either as electrodes, additives, separators, or hosts. This review summarizes recent advances in the synthesis, fundamental properties and composites of MXene and highlights the state‐of‐the‐art electrochemical performance of MXene‐based electrodes/devices. The progresses in the field of supercapacitors and Li‐ion batteries, Li‐S batteries, Na‐ and other alkali metal ion batteries are reviewed, and current challenges and new opportunities for MXenes in this surging energy storage field are presented. In the focus of interest is the possibility to boost device‐level performance, particularly that of rechargeable batteries, which are of utmost importance in future energy technologies. Very recently, the 2019 Nobel Prize in Chemistry was awarded to the inventors of the Li‐ion battery. For sure, this will provide an additional stimulation to study fundamental aspects of electrochemical energy storage.

Designing lightweight nanostructured aerogels for high‐performance electromagnetic interference (EMI) shielding is crucial yet challenging. Ultrathin cellulose nanofibrils (CNFs) are employed for assisting in building ultralow‐density, robust, and highly flexible transition metal carbides and nitrides (MXenes) aerogels with oriented biomimetic cell walls. A significant influence of the angles between oriented cell walls and the incident EM wave electric field direction on the EMI shielding performance is revealed, providing an intriguing microstructure design strategy. MXene “bricks” bonded by CNF “mortars” of the nacre‐like cell walls induce high mechanical strength, electrical conductivity, and interfacial polarization, yielding the resultant MXene/CNF aerogels an ultrahigh EMI shielding performance. The EMI shielding effectiveness (SE) of the aerogels reaches 74.6 or 35.5 dB at a density of merely 8.0 or 1.5 mg cm^–3, respectively. The normalized surface specific SE is up to 189 400 dB cm² g^–1, significantly exceeding that of other EMI shielding materials reported so far.

Rechargeable lithium‐sulfur (Li‐S) batteries have attracted significant research attention due to their high capacity and energy density. However, their commercial applications are still hindered by challenges such as the shuttle effect of soluble lithium sulfide species, the insulating nature of sulfur, and the fast capacity decay of the electrodes. Various efforts are devoted to address these problems through questing more conductive hosts with abundant polysulfide chemisorption sites, as well as modifying the separators to physically/chemically retard the polysulfides migration. Two dimensional transition metal carbides, carbonitrides and nitrides, so‐called MXenes, are ideal for confining the polysulfides shuttling effects due to their high conductivity, layered structure as well as rich surface terminations. As such, MXenes have thus been widely studied in Li‐S batteries, focusing on the conductive sulfur hosts, polysulfides interfaces, and separators. Therefore, in this review, we summarize the significant progresses regarding the design of multifunctional MXene‐based Li‐S batteries and discuss the solutions for improving electrochemical performances in detail. In addition, challenges and perspectives of MXenes for Li‐S batteries are also outlined. image

Transparent conductive electrodes (TCEs) with a high figure of merit (FOM_e, defined as the ratio of transmittance to sheet resistance) are crucial for transparent electronic devices, such as touch screens, micro-supercapacitors, and transparent antennas. Two-dimensional (2D) titanium carbide (Ti₃C₂T_x), known as MXene, possesses metallic conductivity and a hydrophilic surface, suggesting dispersion stability of MXenes in aqueous media allowing the fabrication of MXene-based TCEs by solution processing. However, achieving high FOM_e MXene TCEs has been hindered mainly due to the low intrinsic conductivity caused by percolation problems. Here, we have managed to resolve these problems by (1) using large-sized Ti₃C₂T_x flakes (∼12.2 μm) to reduce interflake resistance and (2) constructing compact microstructures by blade coating. Consequently, excellent optoelectronic properties have been achieved in the blade-coated Ti₃C₂T_x films, i.e., a DC conductivity of 19 325 S cm^-1 at transmittances of 83.4% (≈6.7 nm) was obtained. We also demonstrate the applications of Ti₃C₂T_x TCEs in transparent Joule heaters and the field of supercapacitors, showing an outstanding Joule heating effect and high rate response, respectively, suggesting enormous potential applications in flexible, transparent electronic devices.

Over the recent years, several Re(I) organometallic compounds have been shown to be toxic to various cancer cell lines. However, these compounds lacked sufficient selectivity towards cancer tissues to be used as novel chemotherapeutic agents. In this study, we probe the potential of two known N,N-bis(quinolinoyl) Re(I) tricarbonyl complex derivatives, namely Re(I) tricarbonyl [N,N-bis(quinolin-2-ylmethyl)amino]-4-butane-1-amine (Re–NH₂) and Re(I) tricarbonyl [N,N-bis(quinolin-2-ylmethyl)amino]-5-valeric acid (Re–COOH), as photodynamic therapy (PDT) photosensitizers. Re–NH₂ and Re–COOH proved to be excellent singlet oxygen generators in a lipophilic environment with quantum yields of about 75%. Furthermore, we envisaged to improve the selectivity of Re–COOHvia conjugation to two types of peptides, namely a nuclear localization signal (NLS) and a derivative of the neuropeptide bombesin, to form Re–NLS and Re–Bombesin, respectively. Fluorescent microscopy on cervical cancer cells (HeLa) showed that the conjugation of Re–COOH to NLS significantly enhanced the compound's accumulation into the cell nucleus and more specifically into its nucleoli. Importantly, in view of PDT applications, the cytotoxicity of the Re complexes and their bioconjugates increased significantly upon light irradiation. In particular, Re–Bombesin was found to be at least 20-fold more toxic after light irradiation. DNA photo-cleavage studies demonstrated that all compounds damaged DNA via singlet oxygen and, to a minor extent, superoxide production.