Interface Engineering of Anchored Ultrathin TiO₂/MoS₂ Heterolayers for Highly-Efficient Electrochemical Hydrogen Production

An efficient self-standing hydrogen evolution electrode was prepared by in situ growth of stacked ultrathin TiO₂/MoS₂ heterolayers on carbon paper (CP@TiO₂@MoS₂). Owing to the high overall conductivity, large electrochemical surface area and abundant active sites, this novel electrode exhibits an excellent performance for hydrogen evolution reaction (HER). Remarkably, the composite electrode shows a low Tafel slope of 41.7 mV/dec, and an ultrahigh cathodic current density of 550 mA/cm² at a very low overpotential of 0.25 V. This work presents a new universal strategy for the construction of effective, durable, scalable, and inexpensive electrodes that can be extended to other electrocatalytic systems

Interface Engineering of Anchored Ultrathin TiO₂/MoS₂ Heterolayers for Highly-Efficient Electrochemical Hydrogen Production

An efficient self-standing hydrogen evolution electrode was prepared by in situ growth of stacked ultrathin TiO₂/MoS₂ heterolayers on carbon paper (CP@TiO₂@MoS₂). Owing to the high overall conductivity, large electrochemical surface area and abundant active sites, this novel electrode exhibits an excellent performance for hydrogen evolution reaction (HER). Remarkably, the composite electrode shows a low Tafel slope of 41.7 mV/dec, and an ultrahigh cathodic current density of 550 mA/cm² at a very low overpotential of 0.25 V. This work presents a new universal strategy for the construction of effective, durable, scalable, and inexpensive electrodes that can be extended to other electrocatalytic systems

All-Inorganic Perovskite Solar Cells

The research field on perovskite solar cells (PSCs) is seeing frequent record breaking in the power conversion efficiency (PCE). However, organic–inorganic hybrid halide perovskites and organic additives in common hole-transport materials (HTMs) exhibit poor stability against moisture and heat. Here we report the successful fabrication of all-inorganic PSCs without any labile or expensive organic components. The entire fabrication process can be operated in ambient environment without humidity control (e.g., a glovebox). Even without encapsulation, the all-inorganic PSCs present no performance degradation in humid air (90–95% relative humidity, 25 °C) for over 3 months (2640 h) and can endure extreme temperatures (100 and −22 °C). Moreover, by elimination of expensive HTMs and noble-metal electrodes, the cost was significantly reduced. The highest PCE of the first-generation all-inorganic PSCs reached 6.7%. This study opens the door for next-generation PSCs with long-term stability under harsh conditions, making practical application of PSCs a real possibility