Ligand Effect of PdRu on Pt‐Enriched Surface for Glucose Complete Electro‐Oxidation to Carbon Dioxide and Abiotic Direct Glucose Fuel Cells

Author:

Guan Yichi12,Su Dezhi2,Zhang Yan3,Zhang Bowen1,Liu Yanyi2,Liu Pengcheng2,Ban Lishou2,Qin Tao2,Wang Kaili4,Chu Ganghui1,Liu Xijun5,He Jia2ORCID

Affiliation:

1. Laboratory of Xinjiang Native Medicinal and Edible Plant Resources Chemistry Kashi University Kashi 844008 China

2. School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 China

3. College of Chemistry Research Center for Analytical Sciences Central Laboratory Nankai University Tianjin 300071 China

4. School of Chemistry & Chemical Engineering and Environmental Engineering Weifang University Weifang 261061 China

5. State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures School of Resources Environment and Materials Guangxi University Nanning 530004 China

Abstract

AbstractThe development of advanced electrocatalysts for the abiotic direct glucose fuel cells (ADGFCs) is critical in the implantable devices in living organisms. The ligand effect in the Pt shell‐alloy core nanocatalysts is known to influence the electrocatalytic reaction in interfacial structure. Herein, we reported the synthesis of ternary Pt@PdRu nanoalloy aerogels with ligand effect of PdRu on Pt‐enriched surface through electrochemical cycling. Pt@PdRu aerogels with optimized Pt surface electronic structure exhibited high mass activity and specific activity of Pt@PdRu about 450 mA mgPt−1 and 1.09 mA cm−2, which were 1.4 and 1.6 times than that of commercial Pt/C. Meanwhile, Pt@PdRu aerogels have higher electrochemical stability comparable to commercial Pt/C. In‐situ FTIR spectra results proved that the glucose oxidation reaction on Pt@PdRu aerogels followed the CO‐free direct pathway reaction mechanism and part of the products are CO2 by completed oxidation. Furthermore, the ADGFC with Pt@PdRu ultrathin anode catalyst layer showed a much higher power density of 6.2 mW cm−2 than commercial Pt/C (3.8 Mw cm−2). To simulate the blood fuel cell, the Pt@PdRu integrated membrane electrode assembly was exposed to glucose solution and a steady‐state open circuit of approximately 0.6 V was achieved by optimizing the glucose concentration in cell system.

Publisher

Wiley

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