A new publication from Opto-Electronic Advances, 10.29026/oea.2022.210105 discusses other pathways towards a more sustainable electrocatalyst for efficient hydrogen technology.
Credit: OEA
A new publication from Opto-Electronic Advances, 10.29026/oea.2022.210105 discusses other pathways towards a more sustainable electrocatalyst for efficient hydrogen technology.
When fossil fuels are burned, massive amounts of carbon dioxide, a greenhouse gas, are released into the atmosphere. Greenhouse gases, which trap heat in the Earth’s atmosphere, are to blame for global warming. Sea level rise, harsh weather, biodiversity loss, species extinction, food scarcity, worsening health, and increased poverty are all risks associated with global average warming of above 1.5 degrees Celsius.
Slowing global warming before it transforms the Earth into something unrecognizable is one of the most pressing challenges confronting humanity today. A critical part of addressing such climate changes is reducing the use of fossil fuels and shifting toward renewable energy sources with zero or negative carbon emissions. The good news is that numerous nations are already making efforts to address this issue. For example, many countries have established challenging goals for reducing their reliance on fossil fuels and converting to renewable energy. Solar, geothermal, hydroelectric, wind and biomass are examples of renewable energy sources that can produce energy without accelerating global warming.
The world was in search of a suitable substitute for fossil fuels. Meanwhile, the discovery of the element hydrogen served as a key turning point. Things started to change after the invention of the hydrogen element, researchers came to know that this element is an effective energy carrier and can be a good substitute for fossil fuels. But there was an issue: finding hydrogen in a free state is impossible. As it is a highly reactive non-metal, it never exists freely in nature and is only produced from other sources of energy.
Then a method called electrochemical oxidation/reduction of radicals at electrodes which is green, environmentally friendly, and sustainable came as a saviour in the production of hydrogen, ammonia, hydrocarbons, and other fuels. Mostly, the electrochemical fuel generation for hydrogen and oxygen is carried out through the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), respectively.
But this hydrogen technology requires highly active and stable catalysts for the HER, and platinum (Pt), a rare element, is used in water-splitting devices. This catalyst, Pt, is making this technology much more expensive, and also, platinum production involves toxic chemicals that impact our ecosystem.
Also, due to the non-local concentration of radicals around the electrocatalyst (Pt), the speed of the reaction seems to be very slow. While speeding up this reaction is possible by bringing up the radical concentration via large electrode potential with the help of electricity and this solution again costs high.
The authors of this article have developed a physical and versatile design approach to boost the electrocatalytic fuel generation performance to a wide range through their high-performance electrodes (LIPSS). They say that “The hierarchical LIPSSs on electrodes with periodic ridges and grooves of 100-300 nm widths must be covered with spherical nanoparticles (NPs) sized 3-94 nm diameters and then the localized electric field-induced enhancement in the reagent concentration effect at these periodic ridges and NPs could considerably enhance the performance of electrochemical fuel generation of HER and OER.”
In experiments to test the performance of this catalyst, the authors found out that by using this optimized morphology of LIPSS pattern, the current electrode achieves the highest hydrogen generation rate of about 3×1016 molecules cm-2s-1 at a current density of 10 mA/cm2. This value is achieved with ~45% less electrode potential than that of the Ni foam electrode without any LIPSS pattern. The precise and controlled fabrication of LIPSS on electrodes could significantly improve their performance as a sustainable electrocatalyst for efficient hydrogen generation. On the LIPSS patterned Ni foam substrate, the HER model electrocatalyst demonstrated 130 mV (40%) of lower 10 overpotentials in the HER and high stability. Furthermore, the OER model electrocatalyst on the LIPSS patterned NF substrate required 100 mV (25%) more 10 overpotentials in the OER with improved stability.
Additionally, when two LIPSS patterned electrodes were assembled simultaneously as anode and cathode in a cell, a low electric potential of 330 mV is enough to drive 10 mA/cm2 in the overall water splitting figure, compared to a similar cell made of pristine Ni foam electrodes. The patterned LIPSS electrocatalysts operate at significantly lower electrical potentials, demonstrating that the femtosecond laser patterning approach has a high likelihood of producing green catalysts.
Based on the above process, it is believed that the new insights presented in this study would pave the way for the demonstration of a single-step, fast, and better physical approach to electrode surface patterning that can be applied to any metal and semiconductor catalysts to reduce the required electrical power in various electrochemical reactions.
According to recent findings from the Chinese Academy of Sciences (CAS), Li and his research group are getting closer to achieving this objective. Their technique is still in the research stage but appears to be a promising source of power. Creating a so-called hydrogen-extracting catalyst that is reliable and sustainable for the Earth is the ultimate ambition. The authors of this article look forward to seeing their method on the market in the next few years, and to see its impact grow around the world.
Keywords: electric field localization / hotspot formation / laser-induced periodic surface structures / electrochemical fuel generation / overall water splitting
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Dr Sajed Saraj received his PhD from the Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences. He is currently an Assistant Professor in the GPL Photonics Laboratory at CIOMP. His current research focuses on Pulsed Laser ablation in liquid using an external field to fabricate thin films/colloidal solutions of various types of nanomaterials for water-splitting applications.
Prof. LI Wei’s international research group in the Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences has a broad interest in nanophotonics, thermal photonics, light-matter interactions, and their applications in next-generation energy and information technologies. His work has appeared in journals such as Nature Photonics, Nature Nanotechnology, Nature Review Materials, Nature Communications, Nature Materials, Science, Joule, Nano Letters, PRL, and Light: Science & Applications. His research has been widely covered in the media, including Phys.org, Science Daily, Science Beta, IEEE Spectrum, Nature Materials, CE& News, Science, Science News, and the BBC. Prof. LI Wei was named to MIT Technology Review Asia’s latest list of Innovators Under 35. “Prof. LI achieved many fundamental breakthroughs in multifunctional integrated photodetection devices, photonic and thermodynamic control of thermal radiation, radiative cooling, and energy harvesting,” according to the magazine, which was published in mid-November.
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Opto-Electronic Advances (OEA) is a high-impact, open access, peer reviewed monthly SCI journal with an impact factor of 8.933 (Journal Citation Reports for IF2021). Since its launch in March 2018, OEA has been indexed in SCI, EI, DOAJ, Scopus, CA and ICI databases over the time and expanded its Editorial Board to 36 members from 17 countries and regions (average h-index 49).
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Article reference: Saraj CS, Singh SC, Verma G, Rajan RA, Li W et al. Laser-induced periodic surface structured electrodes with 45% energy saving in electrochemical fuel generation through field localization. Opto-Electron Adv 5, 210105 (2022). doi: 10.29026/oea.2022.210105
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DOI
10.29026/oea.2022.210105
