高电容AC-NiMo LDH复合电极作为高效解耦水电解的氧化还原介质

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL
Jia Lu , Rongcheng Wan , Suili Shi , Jixu Han , Yanbing Li , Baichuan He , Zhiliang Jin , Guorong Wang
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引用次数: 0

摘要

层状双氢氧化物作为一种高效的氧化还原介质,在解耦电解水裂解制氢系统中表现出明显的优势。然而,其固有的低电导率对其广泛应用构成了重大挑战。本文以活性炭为生长基质,采用水热合成的方法合成了复合AC-NiMo LDH氧化还原介质(RM)。电化学测试表明,AC-NM LDH在电流密度为1 a g−1时的比电容为676.3 F g−1(是NiMo LDH的2.28倍),具有优异的性能。此外,该复合电极在2 mA cm−2条件下具有400 s的缓冲能力。在传统耦合系统中,1.53 V的必要输入电压被分离为两个较低的输入电压,去耦系统中H2/O2的演化分别为1.44/0.29 V。此外,经过60次循环测试,其电池电压几乎没有变化。与传统的耦合系统相比,这种结构降低了总能耗,为安全、高效的制氢建立了技术上可行的途径
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-capacitance AC-NiMo LDH composite electrode as redox mediator for efficient decoupled water electrolysis
Layered double hydroxides (LDHs), serving as an efficient redox mediator, has exhibit distinct advantages in the decoupled electrolytic water splitting hydrogen production system. However, its intrinsic low conductivity poses a significant challenge to its broader application. Here, a composite AC-NiMo LDH redox mediator (RM) was synthesized using activated carbon as the growth substrate through a hydrothermal synthesis method involving water. Electrochemical testing shows that the AC-NM LDH10 has excellent performance with a specific capacitance of 676.3 F g−1 at a current density of 1 A g−1 (is 2.28 times that of NiMo LDH). In addition, this composite RM electrode exhibited a high buffering capacity for 400 s under 2 mA cm−2 during the decoupled H2/O2 evolution. In the conventional coupled system, the necessary input voltage of 1.53 V was separated into two lower ones, 1.44/0.29 V for H2/O2 evolutions in the decoupled system, respectively. Furthermore, after 60 cycles of testing, there was almost no change in its cell voltage. This architecture reduces total energy consumption relative to conventional coupled systems, establishing a technologically viable pathway for safe, high-efficiency hydrogen production
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来源期刊
CiteScore
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
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