A self-powered system to electrochemically generate ammonia driven by palladium single atom electrocatalyst

SusMat Pub Date : 2024-08-21 DOI:10.1002/sus2.237
Hao Hu, Shuyuan Pan, Zhiyong Ma, Kaiyi Liu, Yi Li, Haifeng Bao, Chengwei Deng, Fang Luo, Zehui Yang
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Abstract

The utilization of single atoms (SAs) as trifunctional electrocatalyst for nitrogen reduction, oxygen reduction, and oxygen evolution reactions (NRR, ORR, and OER) is still a formidable challenge. Herein, we devise one-pot synthesized palladium SAs stabilized on nitrogen-doped carbon palladium SA electrocatalyst (Pd-SA/NC) as efficient trifunctional electrocatalyst for NRR, ORR, and OER. Pd-SA/NC performs a robust catalytic activity toward NRR with faradaic efficiency of 22.5% at −0.25 V versus reversible hydrogen electrode (RHE), and the relative Pd utilization efficiency is enhanced by 17-fold than Pd-NP/NC. In addition, the half-wave potential reaches 0.876 V versus RHE, amounting to a 58-time higher mass activity than commercial Pt/C. Moreover, the overpotential at 10 mA cm−2 is as low as 287 mV for Pd-SA/NC, outperforming the commercial IrO2 by 360 times in turnover frequency at 1.6 V versus RHE. Accordingly, the assembled rechargeable zinc-air battery (ZAB) achieves a maximum power density of 170 mW cm−2, boosted by 2.3 times than Pt/C–IrO2. Two constructed ZABs efficiently power the NRR-OER system to electrochemically generate ammonia implying its superior trifunctionality.

Abstract Image

由钯单原子电催化剂驱动的电化学生成氨的自供电系统
利用单原子(SAs)作为氮还原、氧还原和氧进化反应(NRR、ORR 和 OER)的三功能电催化剂仍是一项艰巨的挑战。在此,我们设计了稳定在掺氮碳钯SA电催化剂(Pd-SA/NC)上的一锅合成钯SA,作为氮还原、氧还原和氧进化反应的高效三功能电催化剂。Pd-SA/NC 对 NRR 具有很强的催化活性,在 -0.25 V 电压下与可逆氢电极(RHE)相比,其远红外效率为 22.5%,钯的相对利用效率比 Pd-NP/NC 提高了 17 倍。此外,与 RHE 相比,半波电位达到 0.876 V,质量活性比商用 Pt/C 高出 58 倍。此外,Pd-SA/NC 在 10 mA cm-2 时的过电位低至 287 mV,在 1.6 V 相对于 RHE 时的周转频率比商用 IrO2 高出 360 倍。因此,组装后的可充电锌空气电池(ZAB)可达到 170 mW cm-2 的最大功率密度,是 Pt/C-IrO2 的 2.3 倍。两个已构建的锌空气电池为 NRR-OER 系统提供了高效的电能,使其能够电化学生成氨,这表明锌空气电池具有卓越的三重功能。
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