Catalyst frees hydrogen from seawater

Harvesting hydrogen gas from water through electrolysis could lead to a renewable source of fuel. For a small island nation like Singapore, though, fresh water is a precious resource. So, electrolysis researchers there have turned their attention to the sea. They have now developed a catalyst that helps to electrolyse seawater with record-breaking efficiency, generating oxygen and hydrogen that could eventually feed fuel cells (Adv. Mater. 2018, DOI: 10.1002/adma.201707261). The system is powered by solar electricity, producing hydrogen from sunlight with an overall efficiency of 17.9%. “As far as we know, that’s the highest efficiency for seawater,” says Bin Liu of Nanyang Technological University, who was part of the research team. The oceans contain a vast store of hydrogen atoms but freeing them by electrolysis is a huge challenge. In an electrolyser, the current used to split briny water usually turns chloride ions into unwanted chlorine gas, while other ions like calcium and magnesium form insoluble precipitates that clog vital catalysts on the electrodes. The electrolysis reactions can also cause pH changes that corrode electrodes. A cobalt hexacyanoferrate catalyst helps to generate bubbles of oxygen gas at the anode of a solar-powered seawater electrolyser. Meanwhile, a nickel molybdenum sulfide catalyst at the cathode produces hydrogen gas. Liu’s team had previously developed a nickel molybdenum sulfide catalyst that lowered the voltage needed to generate hydrogen gas at a cathode from seawater (Sci. Adv. 2015, DOI:10.1126/sciadv.1500259). Their new catalyst relies on earth-abundant elements to oxidize seawater at an anode, producing oxygen gas, protons, and electrons. To make the anode, the researchers grew nanoneedles of basic cobalt carbonate on carbon fibre cloth. Then they dipped the cloth in 2-methylimidazole, which formed a thin layer of a cobalt-imidazole metal organic framework (MOF) on the outside of the needles. Adding sodium ferrocyanide transformed that layer into cobalt hexacyanoferrate, which inherited the porous nanostructure of the MOF and formed 20-nm-thick catalytic shells around the conducting nanoneedles. With a commercial triple-junction solar cell to supply electricity, the team tested the system using local seawater, adding nothing more than a phosphate buffer to maintain a neutral pH. After 100 hours of continuous operation, the electrolyser had made hydrogen and oxygen, but no chlorine at all. Moreover, its electrodes and catalysts were intact, and its output had fallen by just 10%. In contrast, an electrolyser that used conventional catalysts of platinum and iridium oxide to split the local seawater lost activity much more rapidly, and also produced some chlorine. “The fact that it is selective for oxygen evolution rather than chlorine evolution is very significant,” says Michael E. G. Lyons, an electrocatalysis researcher at Trinity College Dublin. “It’s a very tricky thing to do.” Peter Strasser at the Technical University of Berlin, who has worked on seawater electrolysis, points out that the system has a very low current density. To make useful amounts of hydrogen, the system would need a much higher current density, which could trigger chlorine evolution or other unwanted side reactions. “Problems arise when you go to high current densities,” he says. Liu says that initial tests at higher current densities have not produced any chlorine. But he acknowledges that the system’s performance could be improved. Using fresh water, for example, solar-powered electrolysers have reached solar-to-hydrogen efficiencies of more than 30% (Nat. Commun. 2016, DOI: 10.1038/ncomms13237). Liu’s team is now working with researchers at the Dalian Institute of Chemical Physics to develop their system into a prototype device for generating hydrogen.

Chemical & Engineering News, 30 March 2018 ; http://pubs.acs.org/cen/news

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