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(Invited) Photoelectrochemical Hydrogen Generation Derived from Water Dissociation Under Supercontinuum Solar Light (25)

机译:(邀请)SuperContinuum Solar Light下的水解离(25)下衍生的光电化学氢气

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We created a two-compartment cell (2CC) separated by a bipolar membrane (BPM) sandwiched between through-holed electrodes (THEs) assembly (BPMTHEA-2CC) based on the Golden Role for sustainable water splitting derived from water dissociation (WD) with a dual chemical bias (CB). The BPMTHEA-2CC provides an infinite supply of active reaction species, H~+ and OH~-, from water with an opposite bidirectional charge separation under appropriate applied voltage conditions. We have achieved hydrogen generation derived from WD with BPMTHEA-2CC using an oxygen evolving reaction active TH dimensionally stable anode (De Nora Permelec Ltd) prepared on Pt gauze. Liberated gas was analyzed using a gas chromatograph equipped with a MS-5A column and a thermal conductive detector (TCD). We succeeded in detecting appropriate amounts of molecular hydrogen generated in the cathode of a large-sized BPMTHEA-2CC, anolyte (water)|TH anode|BPM|TH cathode|catholyte (water), by imposing a voltage with less than the theoretical 1.23 V for water splitting at room temperature. We disprove the theory of water electrolysis established for hundreds of years. However, we still require external voltage for water electrolysis. Instead of external voltage, we have harnessed supercontinuum solar light throughout by designing optical tandem, wavelength multiplexing. Zero-bias photocurrent was observed by applying TH n-type semiconductor photoanodes to BPMTHEA-2CC. WD at the junction of BPM is considered to be originated in second Wien effect. Thus Au nanoparticle (Au-NP) was introduced into the junction of BPM to carry out plasmon-induced (PI) WD. With mixing different sizes of Au NPs, a wide range of absorption wavelengths would be attainable. Preliminary results obtained using Au-NP modified BPMTHEA-2CC were reported with two plausible mechanisms. A simple 4-port chamber has been developed to measure hydrogen concentrations down to 7.5 ppm and was used to demonstrate PEC zero bias hydrogen generation with harnessing supercontinuum solar light.
机译:我们创建了一种由双极膜(BPM)分开的双隔室细胞(2CC),基于可持续水分离(WD)的可持续水分分裂的金色作用夹在通孔电极(BPMTHEA-2CC)之间。双化学偏见(CB)。 BPMTHEA-2CC提供无限的活性反应物种,H〜+和OH〜 - ,从水中的水,在适当的施加电压条件下具有相反的双向电荷分离。我们已经使用在Pt纱布上制备的氧不舒服的反应活性Th维度稳定的阳极(De Nora Permelec Ltd)来实现衍生自Wd的氢气。使用配备有MS-5A柱和导热检测器(TCD)的气相色谱仪进行分析释放的气体。通过施加小于理论为1.23的电压,我们成功地检测了大尺寸的BPMTHEA-2CC,阳极电解液(水)阴极电解液(水)阴极电解液(水)的阴极中产生的适当量的分子氢。 v用于在室温下分裂。我们反驳了数百年的水电解理论。但是,我们仍然需要外部电压进行水电解。除了外部电压而不是外部电压,通过设计光学串联,波长多路复用来利用SuperContinuum Slay光。通过将N型半导体光阳极施加至BPMTHEA-2CC,观察到零偏置光电流。在BPM的交界处被认为是第二次Wien效应的WD。因此,将Au纳米颗粒(Au-NP)引入BPM的结射到进行等离子体诱导的(PI)Wd。通过混合不同尺寸的Au nps,可以达到各种吸收波长。报告了使用Au-NP改性BPMTHEA-2CC获得的初步结果,具有两个合理的机制。已经开发了一种简单的4端口室以测量氢气浓度降至7.5ppm,并用于展示具有利用超级连续太阳光的PEC零偏压产生。

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