Achieving high-proportioned 1T-MoS2 within heterostructures derived from polymolybdate-based complex for boosting electrocatalytic hydrogen evolution and oxygen evolution

IF 8.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Chinese Chemical Letters Pub Date : 2025-08-01 Epub Date: 2024-07-02 DOI:10.1016/j.cclet.2024.110197
Zhihan Chang , Yuchen Zhang , Yuan Tian , Xiuli Wang
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Abstract

The fabrication of bifunctional electrocatalysts for hydrogen and oxygen evolution in aqueous environment has far-reaching significance. Especially, reasonable interface process regulation toward heterogeneous composites can make full use of the active sites and improve the electrocatalytic activity. In this study, we designed and synthesized NiS2-MoS2-based heterogeneous composites as efficient and stable electrocatalysts for hydrogen and oxygen evolution in alkaline electrolyte. The heterostructure was obtained by one-step hydrothermal ulfurization operation towards polymolybdate-based metal-organic complex. The composition and nanostructures can be tailored by modulating experiment parameter, realizing the phase-controlled synthesis and interface regulation: (1) High-percentage of 1T-MoS2 can be achieved via selecting appropriate vulcanization time and thiourea concentration, benifiting for the higher electroconductivity and more active sites; (2) Regular and orderly vulcanization time promotes the gradual growth and aggregation of nanosheets; (3) The existence of nickel hydroxide improves the electrocatalytic stability for oxygen production performance. The optimized heterogeneous interfaces provide sufficient active sites and accelerate electron transfer. Consequently, the optimal heterogeneous nanosheets present low overpotentials of 33 and 122 mV at the catalytic current densities of 10 mA/cm2 for HER and OER, respectively.

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在聚钼酸盐基复合材料衍生的异质结构中实现高比例 1T-MoS2,促进电催化氢进化和氧进化
制备水环境中析氢、析氧双功能电催化剂具有深远的意义。特别是对非均相复合材料进行合理的界面工艺调节,可以充分利用活性位点,提高电催化活性。在本研究中,我们设计并合成了nis2 - mos2基非均相复合材料,作为碱性电解质中高效、稳定的析氢、析氧电催化剂。对多钼酸盐基金属有机配合物进行一步水热硫化得到异质结构。通过调节实验参数,可以调整其组成和纳米结构,实现相控合成和界面调节:(1)选择合适的硫化时间和硫脲浓度,可以获得较高的1T-MoS2百分比,有利于获得更高的电导率和更多的活性位点;(2)规律有序的硫化时间促进纳米片的逐渐生长和聚集;(3)氢氧化镍的存在提高了电催化制氧性能的稳定性。优化后的异质界面提供了充足的活性位点,加速了电子的转移。因此,在HER和OER的催化电流密度为10 mA/cm2时,最佳的非均相纳米片的过电位分别为33和122 mV。
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来源期刊
Chinese Chemical Letters
Chinese Chemical Letters 化学-化学综合
CiteScore
14.10
自引率
15.40%
发文量
8969
审稿时长
1.6 months
期刊介绍: Chinese Chemical Letters (CCL) (ISSN 1001-8417) was founded in July 1990. The journal publishes preliminary accounts in the whole field of chemistry, including inorganic chemistry, organic chemistry, analytical chemistry, physical chemistry, polymer chemistry, applied chemistry, etc.Chinese Chemical Letters does not accept articles previously published or scheduled to be published. To verify originality, your article may be checked by the originality detection service CrossCheck.
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