Positioning hydrogen reaction sites by constructing CdS/CoNiMoS4 heterojunctions for efficient photocatalytic hydrogen evolution

被引:5
|
作者
Varma, Pooja [1 ]
Chava, Rama Krishna [2 ]
Liu, Chunli [3 ]
Kim, Tae Kyu [4 ]
Amaranatha Reddy, D. [1 ]
机构
[1] Indian Inst Informat Technol Design & Mfg, Dept Sci, Kurnool 518008, Andhra Pradesh, India
[2] Yeungnam Univ, Coll Nat Sci, Dept Chem, 280 Daehak Ro, Gyongsan 38541, Gyeongsan, South Korea
[3] Hankuk Univ Foreign Studies, Oxide Res Ctr, Dept Phys, Yongin 17035, South Korea
[4] Yonsei Univ, Dept Chem, Seoul 03722, South Korea
关键词
CDS; COCATALYST; STABILITY;
D O I
10.1039/d3dt02843g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The high gravimetric energy density of hydrogen makes it an ideal chemical fuel to address the issues of fossil fuel depletion and environmental pollution. Even though transition metal sulfides (TMSs) have been extensively investigated as substitutes for noble metals, their effectiveness is still doubtful for practical applications. Herein, we introduce a facile and general strategy to fabricate heterojunctions with CdS nanorods and a multimetallic transition metal sulfide (CoNiMoS4) for enhanced photocatalytic activity. The CdS/CoNiMoS4 heterojunction will serve as a dual-function photocatalyst with enhanced visible light absorption capability offered by CdS and high charge transfer efficiency provided by CoNiMoS4 nanostructures. Moreover, CdS/CoNiMoS4 nanostructures exhibit the best photocatalytic performance to generate H-2 with an amount of 31.9 mmol g(-1) h(-1), with a distinguished stability for over 25 h. This synthetic approach may offer a new strategy to create diverse heterojunctions with Earth-abundant multimetallic components, which may broaden their scope of application in catalysis.
引用
收藏
页码:16249 / 16260
页数:12
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