98%
921
2 minutes
20
Proton exchange membrane water electrolysis (PEMWE) is regarded as the most promising technique for the sustainable production of green hydrogen due to its multiple advantages such as high working current density and high hydrogen purity. However, the anodic oxygen evolution reaction (OER) has a significant impact on the overall efficiency of the electrolytic water reaction due to its sluggish kinetics, which has prompted the search for catalysts possessing both high activity and durability. Iridium oxide exhibits excellent stability under acidic conditions but has poor catalytic activity, leading to its inability to meet the strict requirements of large-scale industrial applications. In this work, we have successfully synthesized two-dimensional (2D) 1T-phase manganese-iridium oxide (1T-MnIrO) nanosheets by a molten-alkali mechanochemical method. In 0.5 M HSO, the 1T-MnIrO achieves an overpotential of 274 mV with a low Tafel slope of 70.77 mV dec, and durable stability of 75 h at 10 mA cm. Its mass activity at 1.5 V reversible hydrogen electrode (RHE) is 390 mA mg, 39.6 times higher than that of commercial iridium oxide. When applied in a practical PEMWE system, 1T-MnIrO retains a high current density of 1000 mA cm at a cell voltage of 1.7 V for 500 h. The 1T-MnIrO catalyst can achieve high performance and endurance of PEMWE with only a small amount of Ir, providing a feasible approach to alleviate the problems of low Ir reserves and high prices.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/d5nr02833g | DOI Listing |
ACS Nano
September 2025
College of Materials Science and Engineering, Fuzhou University, Fuzhou 350108, China.
Polymorphic two-dimensional (2D) transition metal dichalcogenides (TMDCs) exhibit diverse properties for optoelectronic applications. Here, utilizing phase-engineered MoTe as a prototypical platform, we comprehensively explored its ultrafast and nonlinear optical properties to complete the fundamental framework of phase-dependent optical phenomena in 2D TMDCs. Starting with the phase-selective synthesis of 2H- and 1T'-MoTe with tailored thicknesses, we revealed their distinct photocarrier relaxation mechanisms using intensive power-/temperature-/thickness-dependent transient absorption spectra (TAS).
View Article and Find Full Text PDFNanoscale
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, Jiangsu, China.
Proton exchange membrane water electrolysis (PEMWE) is regarded as the most promising technique for the sustainable production of green hydrogen due to its multiple advantages such as high working current density and high hydrogen purity. However, the anodic oxygen evolution reaction (OER) has a significant impact on the overall efficiency of the electrolytic water reaction due to its sluggish kinetics, which has prompted the search for catalysts possessing both high activity and durability. Iridium oxide exhibits excellent stability under acidic conditions but has poor catalytic activity, leading to its inability to meet the strict requirements of large-scale industrial applications.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Jiangsu, 215123, P.R. China.
Designing unique electrocatalysts that utilizes carbon dioxide reduction reaction (CORR) for real applications is highly appreciated, yet still suffers from low selectivity, stability, and compatibility. Herein, we first report a new two-dimensional metastable-phase transparent conducting oxide: 1T phase indium tin oxide (m-ITOs) with the space group of P-3m1 (164), which is totally different from that of the stable cubic phase ITO (Ia-3 (206)). The internal indium tin catalytic pairs in m-ITOs trigger the strong electronic coupling, move up the p-band center, and stabilize the adsorption of HCOO* for increased formate production.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
School of Physics and Electronics, Hunan University, Changsha 410082, China.
Atomic-scale elucidation of phase transition pathways in two-dimensional (2D) materials is practically necessary for achieving desired architectures in next-generation devices, yet it remains hindered by insufficient understanding of defect-mediated kinetics. Here, we study the behavior of Se defects in mediating phase transitions in single-layer (SL) VSe grown on Au(111), achieved through controlled thermal annealing and selenium (Se) replenishment. Using scanning tunneling microscopy (STM) and angle-resolved photoemission spectroscopy (ARPES), we find that the initial SL VSe is a 1T phase featuring a substrate-induced moiré superstructure and that several annealing stages lead to two defective, Se-poor phases with an increased in-plane lattice constant.
View Article and Find Full Text PDFJ Phys Chem Lett
July 2025
Institute of Quantum Physics, School of Physics, Central South University, 932 South Lushan Road, Changsha, Hunan 410083, People's Republic of China.
Second-harmonic generation (SHG) in two-dimensional (2D) materials typically requires broken inversion symmetry, posing a fundamental constraint for nonlinear optical applications. Surprisingly, the SHG phenomenon was recently observed in centrosymmetric 1T-phase transition metal disulfide compounds (1T-TMDs), but its underlying mechanism and tunability remain elusive. Here, taking the centrosymmetric 1T-PtS as an example, we investigate the SHG responses and origin, finding a surprising giant SHG response, exhibiting intensities up to 15 times greater than noncentrosymmetric monolayer WS under the same excitation conditions.
View Article and Find Full Text PDF