摘要
Electrode materials are pivotal to advancing the deployment of photoelectrochemical (PEC) seawater splitting. Carbon materials hold great potential for modifying semiconductors to fabricate high-performance photocathodes, but are limited in seawater by the Ca 2+ and Mg 2+ . Herein, a microwave-synthesized carbon dots ( m -CDs) were demonstrated as electron donors in composite photocathode materials to enhance their performance for seawater splitting. The as-prepared m -CDs/CuBi 2 O 4 photocathode exhibited a photocurrent density of 0.183 mA cm −2 at 0.4 V vs. RHE in simulated seawater, which was outperforming the pristine CuBi 2 O 4 (0.102 mA cm −2 ) and hydrothermal-synthesized carbon dots (h-CDs) modified CuBi 2 O 4 (0.106 mA cm −2 ) samples. The structural characterization results show that the surface of m -CDs is rich in acidic groups. These functional groups will significantly increase the H + concentration on the catalyst surface during the HER process, inhibit the rise of surface pH, thereby preventing Ca 2+ /Mg 2+ from forming hydroxides and reducing the catalytic performance. This study not only presents a metal-free carbon material to enhance the photocathode performance for seawater splitting, but also offers a theoretical foundation for the rational design of carbon materials in this field.
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