材料科学
光催化
二硫化钼
光致发光
电子转移
化学工程
钼
纳米技术
催化作用
分析化学(期刊)
光电子学
光化学
复合材料
工程类
冶金
化学
生物化学
色谱法
作者
Wenchao Wang,Sai Zhu,Yingnan Cao,Ying Tao,Xin Li,Donglai Pan,David Lee Phillips,Dieqing Zhang,Ming Chen,Guisheng Li,Hexing Li
标识
DOI:10.1002/adfm.201901958
摘要
Abstract Exploring TiO 2 ‐photocatalysts for sunlight conversion has high demand in artificial photosynthesis. In this work, edge‐enriched ultrathin molybdenum disulfide (MoS 2 ) flakes are uniformly embedded into the bulk of yolk‐shell TiO 2 as a cocatalyst to accelerate photogenerated‐electron transfer from the bulk to the surface of TiO 2 . The as‐formed MoS 2 /TiO 2 (0.14 wt%) hybrids exhibit a high hydrogen evolution rate (HER) of 2443 µmol g −1 h −1 , about 1000% and 470% of that of pristine TiO 2 (247 µmol g −1 h −1 ) and bulk MoS 2 decorated TiO 2 (513 µmol g −1 h −1 ). Such a greatly enhanced HER is attributed to the exposed catalytic edges of the ultrathin MoS 2 flakes with a robust chemical linkage (TiS bond), providing rapid charge transfer channels between TiO 2 and MoS 2 . The catalytic stability is promoted by the antiaggregation of the highly dispersed MoS 2 flakes in the bulk of yolk‐shell TiO 2 . The exponential fitted decay kinetics of time‐resolved photoluminescence (ns‐PL) spectra illustrates that embedding ultrathin MoS 2 flakes in TiO 2 effectively decreases the average lifetime of PL in the MoS 2 /TiO 2 hybrids (τ ave = 4.55 ns), faster than that of pristine TiO 2 (≈7.17 ns) and the bulk MoS 2 /TiO 2 (≈6.13 ns), allowing a superior charge separation and charge trapping process for reducing water.
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