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
Abstract
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
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
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.
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