Au/Ti3C2/g-C3N4 Ternary Composites Boost H2 Evolution Efficiently with Remarkable Long-Term Stability by Synergistic Strategies.

Abstract

The use of novel two-dimensional MXene materials and conventional g-C3N4 photocatalysts to fabricate the composites for hydrogen evolution reaction (HER) has attracted much attention, for which there is plenty of room for the enhancement of hydrogen evolution rates particularly under visible light and photostability. Herein, g-C3N4 was modified by copolymerization of malonamide and melamine and used to fabricate the ternary composites of Au particles and Ti3C2 MXene, and based on the synergistic effect, the composites enhanced the hydrogen evolution rates by 2.1, 99.8, and ∞ times compared with the unmodified g-C3N4 under UV, simulated sunlight, and visible light illumination, respectively. Moreover, the composite exhibited a sustained hydrogen evolution capacity in the cycle test for up to 120 h. Theoretical calculations and experimental results indicated that the hot electrons of Au are injected into the modified g-C3N4 and transferred to Ti3C2 simultaneously along with the photogenerated electrons of the modified g-C3N4 and then further transferred to Au, forming a photogenerated electron transfer channel of Au and modified g-C3N4 → Ti3C2 → Au within the composite. Ti3C2 acts as a bridge for fast separation of photogenerated electrons and holes on Au and modified g-C3N4, playing a key role in the enhanced photocatalytic performance. In addition, the visible light absorption ability of Au also positively contributed to the enhancement of visible light photocatalytic performance by providing hot electrons. Therefore, the selection of suitable cocatalysts for the design of composites is a crucial research direction to improve the photocatalytic performance and photostability of photocatalysts.