Photothermal desalination is a promising approach for seawater purification by harvesting solar energy. Titanium carbide (Ti 3 C 2 T x MXene) membranes have been regarded as potential materials for photothermal desalination by virtue of their excellent light-to-heat conversion. However, achieving a well-balanced synergy between high evaporation rate and good salt resistance remains a significant challenge due to their limited solar absorption and inferior stability. Herein, we report a self-assembled flexible porphyrin-Ti 3 C 2 T x MXene Janus membrane (Janus PMX membrane) for dual-functional enabled photothermal desalination. The self-assembly of porphyrin on MXene not only effectively creates a favorable hydrophobic surface but also simultaneously enables efficient solar utilization. The significant interactions and charge redistribution between MXene and porphyrin lead to a stable hydrophobic/hydrophilic Janus structure with synergistically enhanced photothermal conversion. As a result, the Janus PMX membrane demonstrates highly efficient water pumping, heat localization, vapor generation, and salt resistance during photothermal desalination. This work presents an effective and facile strategy toward advancing a well-performing MXene membrane for efficient seawater desalination.
Development of high‐performance and low‐cost nonprecious metal electrocatalysts is critical for eco‐friendly hydrogen production through electrolysis. Herein, a novel nanoflower‐like electrocatalyst comprising few‐layer nitrogen‐doped graphene‐encapsulated nickel–copper alloy directly on a porous nitrogen‐doped graphic carbon framework (denoted as Nix
Cuy
@ NG‐NC) is successfully synthesized using a facile and scalable method through calcinating the carbon, copper, and nickel hydroxy carbonate composite under inert atmosphere. The introduction of Cu can effectively modulate the morphologies and hydrogen evolution reaction (HER) performance. Moreover, the calcination temperature is an important factor to tune the thickness of graphene layers of the Nix
Cuy
@ NG‐NC composites and the associated electrocatalytic performance. Due to the collective effects including unique porous flowered architecture and the synergetic effect between the bimetallic alloy core and graphene shell, the Ni3Cu1@ NG‐NC electrocatalyst obtained under optimized conditions exhibits highly efficient and ultrastable activity toward HER in harsh environments, i.e., a low overpotential of 122 mV to achieve a current density of 10 mA cm−2 with a low Tafel slope of 84.2 mV dec−1 in alkaline media, and a low overpotential of 95 mV to achieve a current density of 10 mA cm−2 with a low Tafel slope of 77.1 mV dec−1 in acidic electrolyte.
Fe O is regarded as a promising anode material for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) due to its high specific capacity. The large volume change during discharge and charge processes, however, induces significant cracking of the Fe O anodes, leading to rapid fading of the capacity. Herein, a novel peapod-like nanostructured material, consisting of Fe O nanoparticles homogeneously encapsulated in the hollow interior of N-doped porous carbon nanofibers, as a high-performance anode material is reported. The distinctive structure not only provides enough voids to accommodate the volume expansion of the pea-like Fe O nanoparticles but also offers a continuous conducting framework for electron transport and accessible nanoporous channels for fast diffusion and transport of Li/Na-ions. As a consequence, this peapod-like structure exhibits a stable discharge capacity of 1434 mAh g (at 100 mA g ) and 806 mAh g (at 200 mA g ) over 100 cycles as anode materials for LIBs and SIBs, respectively. More importantly, a stable capacity of 958 mAh g after 1000 cycles and 396 mAh g after 1500 cycles can be achieved for LIBs and SIBs, respectively, at a large current density of 2000 mA g . This study provides a promising strategy for developing long-cycle-life LIBs and SIBs.
Single‐atom catalysts (SACs) have received widespread interest for their high atomic efficiency, enriched active sites, excellent catalytic performance, and low cost. However, the agglomeration of single metal atoms and the use of inactive additives for affixing powdery SACs on planar electrodes may reduce the density of active sites, diminish the charge transport to active sites, and thus suppress their performance. Herein, a series of metal–nitrogen–carbon single‐atom aerogels (M‐SAAs, M: Cu, Ni, Au, Ru) are synthesized via a universal strategy, in which the merits of metal organic frameworks and carbon aerogels are perfectly combined to prevent the agglomeration of single metal atoms and overcome the problem of poor electrical conductivity. The as‐prepared M‐SAAs can be directly employed as self‐supporting electrodes for the electrochemical dechlorination of 1,2‐dichloroethane, and outstanding activity and stability are observed. Significantly, the Cu‐SAA with abundant Cu−N4 sites shows an extraordinarily high ethylene production rate of 446 µmol h−1, with a selectivity of 99% and Faradaic efficiency of 64%. Moreover, theoretical calculations are performed to demonstrate the selectivity and activity of different metal active sites. This study provides a new strategy to exploit highly effective SACs and offers an intensive insight into the mechanism of electrochemical dechlorination reactions.
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