Phase-engineered nickel selenide cocatalyst on CdS for enhanced visible-light photocatalytic H2 production

IF 4.4 3区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Yimin Liu , Zhiqing Lu , Wei Lin , Lei Duan , Yuezhou Wei , Deqian Zeng
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Abstract

To improve the efficiency of photocatalytic H2 generation, cocatalysts are commonly utilized to suppress the recombination of photogenerated charge carriers and provide reaction active sites. Herein, four different crystalline phases of nickel selenide were controllably prepared via a simple one-pot approach. The nickel selenide underwent multiple phase transformations at reaction temperatures of 180, 240, 280, and 300 ℃, resulting in orthorhombic, orthorhombic-cubic, cubic, and cubic-hexagonal phases, respectively. Nickel selenides were combined with CdS using an in-situ precipitation method for photocatalytic H2 generation reactions. All four crystalline phases of nickel selenide were found to be effective cocatalysts that boosted the photocatalytic H2 production performance of CdS under visible light. Among these phases, the orthorhombic-cubic NiSe2 demonstrated a superior H2 generation rate of 3039 µmol h−1 g−1, 6.5 times higher than CdS. The effective charge transfer between CdS and nickel selenide was revealed through photoluminescence (PL), electrochemical, and photoelectrochemical analyses. This work introduces a practical approach to designing cost-effectiveness NiSex cocatalysts on metal sulfide semiconductors, leveraging phase control to optimize photocatalytic solar-to-H2 conversion.

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来源期刊
Inorganic Chemistry Communications
Inorganic Chemistry Communications 化学-无机化学与核化学
CiteScore
5.50
自引率
7.90%
发文量
1013
审稿时长
53 days
期刊介绍: Launched in January 1998, Inorganic Chemistry Communications is an international journal dedicated to the rapid publication of short communications in the major areas of inorganic, organometallic and supramolecular chemistry. Topics include synthetic and reaction chemistry, kinetics and mechanisms of reactions, bioinorganic chemistry, photochemistry and the use of metal and organometallic compounds in stoichiometric and catalytic synthesis or organic compounds.
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