کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6464994 1422946 2018 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Synthesis of MoS2 quantum dots cocatalysts and their efficient photocatalytic performance for hydrogen evolution
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Synthesis of MoS2 quantum dots cocatalysts and their efficient photocatalytic performance for hydrogen evolution
چکیده انگلیسی


- Different MoS2 QDs/CdS photocatalysts were successfully synthesized.
- Hydrothermal and liquid exfoliation method was screened and optimized.
- The obtained materials work as efficient visible-light-driven photocatalysts.
- Good stability was observed in cyclic runs of photocatalytic H2 production.
- Higher electrocatalytic activity corresponds to higher photocatalytic activity.

Exploiting noble-metal free cocatalysts is of great importance for water splitting via solar energy. Molybdenum disulfide (MoS2) has been identified as a promising non-precious-metal cocatalyst to replace Pt. Here, two facile synthetic routes including a hydrothermal process and a liquid exfoliation strategy were adopted and screened for finely controlled synthesis of MoS2 QDs cocatalysts and their application in the visible-light photocatalytic hydrogen production. It was confirmed that the MoS2 QDs-L (L is the abbreviation of liquid exfoliation method) as cocatalyst can remarkably enhance the photocatalytic hydrogen activity of CdS under visible-light irradiation. Notably, with lactic acid as a sacrificial agent, the MoS2 QDs-L/CdS photocatalyst achieved an optimal hydrogen production activity with a rate of 1032.1 μmol h−1, which was 2.7 times more effective than that of the corresponding bulk MoS2/CdS (383.5 μmol h−1) and 15.4 times more effective than that of the bare commercial CdS (66.9 μmol h−1). In the meantime, the MoS2 QDs-L/CdS exhibited a good stability of in the cyclic runs for the photocatalytic hydrogen production. Impressively, it was found that a higher electrocatalytic activity of MoS2 QDs-L/CdS is directly consistent with a higher photocatalytic activity of MoS2 QDs-L/CdS during the hydrogen production. These findings will open opportunities for developing low-cost, high efficiency and stable photocatalyst that will find potential applications both in environmental protection and in renewable energy areas.

Exploiting noble-metal free cocatalysts is of great importance for water splitting via solar energy. Molybdenum disulfide (MoS2) has been identified as a promising non-precious-metal cocatalyst to replace Pt. Here, two facile synthetic routes including a hydrothermal process and a liquid exfoliation strategy were adopted and screened for finely controlled synthesis of MoS2 QDs cocatalyst and their application in the visible-light photocatalytic hydrogen production. It was confirmed that the MoS2 QDs-L (L is the abbr'eviation of liquid exfoliation method) as cocatalyst can remarkably enhance the photocatalytic hydrogen activity of CdS under visible-light irradiation. Notably, with lactic acid as a sacrificial agent, the MoS2 QDs-L/CdS photocatalyst achieved an optimal hydrogen production activity with a rate of 1032.1 μmol h−1, which was 2.7 times more effective than that of the corresponding bulk MoS2/CdS (383.5 μmol h−1) and 15.4 times more effective than that of the bare commercial CdS (66.9 μmol h−1). In the meantime, the MoS2 QDs-L/CdS exhibited a good stability of in the cyclic runs for the photocatalytic hydrogen production. Impressively, it was found that a higher electrocatalytic activity of MoS2 QDs-L/CdS is directly consistent with a higher photocatalytic activity of MoS2 QDs-L/CdS during the hydrogen production. These findings will open opportunities for developing low-cost, high efficiency and stable photocatalyst that will find potential applications both in environmental protection and in renewable energy areas.86

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Engineering Journal - Volume 332, 15 January 2018, Pages 449-455
نویسندگان
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