School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PR China.
J Colloid Interface Sci. 2022 Mar;609:686-697. doi: 10.1016/j.jcis.2021.11.065. Epub 2021 Nov 17.
The use of semiconductors to construct heterojunctions to suppress the rapid recombination of photogenerated charges and holes is considered to be an effective way to improve the efficiency of photocatalytic hydrogen evolution. Herein, cobalt sulfide (CoS) nanoparticles are cultivated in situ in the folds of three-dimensional flower-like nickel-aluminium layered double hydroxides (NiAl-LDHs) using a facile solvothermal method. The hydrogen production rate of the binary CoS/NiAl-LDH heterojunction reaches 3678.59 μmol/g/h, which is 83.74 and 22 times the rates of CoS and NiAl-LDH, respectively. The unique three-dimensional structure of NiAl-LDH facilitates the growth of CoS and shortens the transfer pathway of photogenerated electrons. More importantly, the built-in electric field formed at the interface and the S-type charge transport mechanism caused by the bending of the energy band enhance not only charge separation but also maintain the strong oxidation ability of the holes. In this study, the newly designed S-scheme heterojunction offers a new strategy for enhancing photocatalytic water splitting.
采用半导体构建异质结来抑制光生载流子的快速复合被认为是提高光催化析氢效率的有效方法。在此,通过简便的溶剂热法,在三维花状镍铝层状双氢氧化物(NiAl-LDH)的褶皱中原位生长了硫化钴(CoS)纳米颗粒。二元 CoS/NiAl-LDH 异质结的制氢速率达到 3678.59 μmol/g/h,分别是 CoS 和 NiAl-LDH 的 83.74 倍和 22 倍。NiAl-LDH 的独特三维结构有利于 CoS 的生长并缩短了光生电子的转移路径。更重要的是,界面处形成的内置电场和能带弯曲引起的 S 型电荷传输机制不仅增强了电荷分离,而且保持了空穴的强氧化能力。在这项研究中,新设计的 S 型异质结为增强光催化水分解提供了一种新策略。