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Efficient hydrogen peroxide synthesis from seawater via Na- and Pb-codoped SnSe under moderate temperature gradient

Yuyan Xu, Xinyue Zhang, Yangyang Wan, Bingchao Qin, Jun Pei, Hong Liu, Xiaoxue Song, Shutong Jiang, Zhongti Sun, Yuqiao Zhang, Long Zhang, Yong Liu, Qian Yu, Li‐Dong Zhao, Shun Li, Jianming Zhang

Revista con revisión por paresAfirmaciones fuertes, leer con cuidadoUso en el mundo real

En palabras de los autores

Hydrogen peroxide (H2O2) plays a crucial role in environmental remediation, chemical synthesis, and energy storage. Nevertheless, its industrial production is energy consuming with significant environmental burdens. Here we show a proof-of-concept thermoelectrocatalytic strategy for H2O2 production directly from seawater, driven solely by low-grade waste heat. A low-temperature thermoelectric (TE) material, Na- and Pb-codoped SnSe, is designed as a catalyst that enables efficient H2O2 generation under a moderate temperature gradient (ΔT). This system achieves an H2O2 production rate of 6.1 mmol g−1 h−1 from seawater under ΔT = 120 K, which is competitive with the representative photocatalytic systems. Experimental and theoretical analyses reveal that Na/Pb-codoping improves the TE properties, promotes charge carrier migration under ΔT, and promotes the oxygen reduction reaction toward H2O2 formation. The naturally formed strong electric layer at the catalyst-seawater interface further promotes both reaction kinetics and thermodynamic driving forces. Our finding provides a sustainable route for H2O2 production from seawater using waste heat and demonstrates great potential of TE-catalysis for waste heat utilization. Thermoelectrocatalysis offers a sustainable pathway for chemical synthesis utilizing low-grade waste heat. Here, the authors present a high-performance material design that enables efficient, thermal-gradient-driven catalytic production of H2O2 from seawater without external electrical power.

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Apareció: sábado, 26 de septiembre. Nature Communications. Revista con revisión por pares.

DOI: 10.1038/s41467-026-78104-9