(Press-News.org) To reduce greenhouse gas emissions and combat climate change, the world urgently needs clean and renewable energy sources. Hydrogen is one such clean energy source that has zero carbon content and stores much more energy by weight than gasoline. One promising method to produce hydrogen is electrochemical water-splitting, a process that uses electricity to break down water into hydrogen and oxygen. In combination with renewable energy sources, this method offers a sustainable way to produce hydrogen and can contribute to the reduction of greenhouse gases.
Unfortunately, large-scale production of hydrogen using this method is currently unfeasible due to the need for catalysts made from expensive rare earth metals. Consequently, researchers are exploring more affordable electrocatalysts, such as those made from diverse transition metals and compounds. Among these, transition metal phosphides (TMPs) have attracted considerable attention as catalysts for the hydrogen generating side of the process, known as hydrogen evolution reaction (HER), due to their favorable properties. However, they perform poorly in the oxygen evolution reaction (OER), which reduces overall efficiency. Previous studies suggest that Boron (B)-doping into TMPs can enhance both HER and OER performance, but until now, making such materials has been a challenge.
In a recent breakthrough, a research team led by Professor Seunghyun Lee, including Mr. Dun Chan Cha, from the Hanyang University ERICA campus in South Korea, has developed a new type of tunable electrocatalyst using B-doped cobalt phosphide (CoP) nanosheets. Prof. Lee explains, “We have successfully developed cobalt phosphides-based nanomaterials by adjusting boron doping and phosphorus content using metal-organic frameworks. These materials have better performance and lower cost than conventional electrocatalysts, making them suitable for large-scale hydrogen production.” Their study was published in the journal Small on March 19, 2025.
The researchers used an innovative strategy to create these materials, using cobalt (Co) based metal-organic frameworks (MOFs). “MOFs are excellent precursors for designing and synthesizing nanomaterials with the required composition and structures,” notes Mr. Cha. First, they grew Co-MOFs on nickel foam (NF). They then subjected this material to a post-synthesis modification (PSM) reaction with sodium borohydride (NaBH4), resulting in the integration of B. This was followed up by a phosphorization process using different amounts of sodium hypophosphite (NaH2PO2), resulting in the formation of three different samples of B-doped cobalt phosphide nanosheets (B-CoP@NC/NF).
Experiments revealed that all three samples had a large surface area and a mesoporous structure, key features that improve electrocatalytic activity. As a result, all three samples exhibited excellent OER and HER performance, with the sample made using 0.5 grams of NaH2PO2 (B-CoP0.5@NC/NF) demonstrating the best results. Interestingly, this sample exhibited overpotentials of 248 and 95 mV for OER and HER, respectively, much lower than previously reported electrocatalysts.
An alkaline electrolyzer developed using the B-CoP0.5@NC/NF electrodes showed a cell potential of just 1.59 V at a current density of 10 mA cm-2, lower than many recent electrolyzers. Additionally, at high current densities above 50 mA cm-2, it even outperformed the state-of-the-art RuO₂/NF(+) and 20% Pt-C/NF(−) electrolyzer, while also demonstrating long-term stability, maintaining its performance for over 100 hours.
Density functional theory (DFT) calculations supported these findings and clarified the role of B-doping and adjusting P content. Specifically, B-doping and optimal P content led to effective interaction with reaction intermediates, leading to exceptional electrocatalytic performance.
“Our findings offer a blueprint for designing and synthesizing next-generation high-efficiency catalysts that can drastically reduce hydrogen production costs,” says Prof. Lee. “This is an important step towards making large-scale green hydrogen production a reality, which will ultimately help in reducing global carbon emissions and mitigating climate change.”
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Reference
DOI: 10.1002/smll.202500334
About Hanyang University ERICA
Hanyang University ERICA (Education Research Industry Cluster at Ansan) is a prominent research-focused campus established in 1979 in Ansan, South Korea. ERICA offers undergraduate and graduate programs. ERICA is renowned for its active industry-university cooperation, offering students hands-on experience through partnerships with various industries. This ensures that graduates are well-prepared to meet societal needs and excel in their respective fields. With state-of-the-art facilities and a supportive learning environment, Hanyang University ERICA empowers students to pursue their passions and contribute meaningfully to society, staying true to the university's founding philosophy of "Love in Deed and Truth."
Website: https://www.hanyang.ac.kr/web/eng/erica-campus1
About Professor Seunghyun Lee
Seunghyun Lee is an associate professor of chemistry at Hanyang University, South Korea. He earned his Ph.D. from Rice University under Prof. Jason H. Hafner and MS from Hanyang University under Prof. Haiwon Lee. Prior to Hanyang University, he was an assistant and associate professor at Gachon University and a post-doctoral researcher at Purdue University under Prof. Joseph Irudayaraj and at Rice University under Prof. Pulickel M. Ajayan. His research centers on plasmonic hybrid nanomaterials, focusing on multi-component heterostructures for photocatalytic and electrocatalytic applications in green energy production.
About Dr. Dun Chan Cha
Dun Chan Cha is pursuing his Ph.D. in Prof. Seunghyun Lee’s group, at Hanyang University. He received his bachelor’s degree from Gachon University, South Korea in 2020 and master’s degree in applied chemistry from Hanyang University, South Korea in 2023. His research interests focus on metal-organic framework derivatives, transition metal phosphides, and nitrides for electrocatalytic water-splitting.
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