University of Houston researchers have reported an inexpensive hybrid catalyst capable of splitting water to produce hydrogen, suitable for large-scale commercialization.

Most systems to split water into its components of hydrogen and oxygen require two catalysts, one to spur a reaction to separate the hydrogen and a second to produce oxygen. The new catalyst, made of iron and dinickel phosphides on commercially available nickel foam, performs both functions.

The Houston researchers said it has the potential to dramatically lower the amount of energy required to produce hydrogen from water while generating a high current density, a measure of hydrogen production. Lower energy requirements means the hydrogen could be produced at a lower cost.

Zhifeng Ren, M.D. is the Anderson Chair Professor of physics at UH and lead author of a paper describing the new catalyst published Friday in Nature Communications. He said, “It puts us closer to commercialization.”

Hydrogen is considered a desirable source of clean energy, in the form of fuel cells to power electric motors or burned in internal combustion engines, along with a number of industrial uses. Because it can be compressed or converted to liquid, it is more easily stored than some other forms of energy, said Ren, who also is a researcher at the Texas Center for Superconductivity at the University of Houston.

But finding a practical, inexpensive and environmentally friendly way to produce large amounts of hydrogen gas, especially by splitting water into its component parts, has long been a challenge.

Most hydrogen is currently produced through steam methane reforming and coal gasification; those methods raise the fuel’s carbon footprint despite the fact that it burns cleanly.

Co-author Shuo Chen, assistant professor of physics at UH explained while traditional catalysts can produce hydrogen from water, they generally rely on expensive platinum group elements. That raises the cost, making large-scale water splitting impractical.

“In contrast, our materials are based on earth abundant elements and exhibit comparable performance with those of platinum group materials,” she added. “It can be potentially scaled-up at low cost, which makes it very attractive and promising for the commercialization of water splitting.”

Researchers said the catalyst remained stable and effective through more than 40 hours of testing.

The new catalyst, they wrote, “proves to be an outstanding bifunctional catalyst for overall water splitting, exhibiting both extremely high OER (oxygen evolution reaction) and HER (hydrogen evolution reaction) activities in the same alkaline electrolyte. Indeed, it sets a new record in alkaline water electrolyzers (1.42 V to afford 10 mA cm-2), while at the commercially practical current density of 500 mA cm-2.”

Previous catalysts have used different materials to spur a reaction to produce the hydrogen than those that are used to produce the oxygen. Ren said the interaction between the iron phosphide particles and the dinickel phosphide particles boosted both reactions. “Somehow a joint effort of the two materials is better than any individual material,” he said.

In addition to Ren and Chen, other authors on the paper include Fang Yu, Haiqing Zhou and Jingying Sun, all with the UH Department of Physics; Fan Qin and Jiming Bao, with the Department of Electrical and Computer Engineering at UH; and Yufeng Huang and William A. Goddard III of the Materials and Process Simulation Center at the California Institute of Technology.

This is excellent news, well worth a bit of acclaim as getting both reactions in a single process is remarkable in itself. Along with the low electricity input it seems to be a winner right out of the lab. Although right out of the lab success is extremely rare, there is an existing demand for hydrogen for industry all the time. If industry picks this up and saves and make money then the hydrogen economy has finally found its legs. That would leave the storage issue and coming up with enough current. Maybe this is a turning point.


Name (required)

Email (required)


Speak your mind