{"title":"富氧空位非晶异质结构镍钴氧化物电催化合成苯甲酸及硝酸还原","authors":"Rushun An, Chunlai Wang, Yandong Li, Yingkai Di, Fusheng Li, Fei Li, Licheng Sun, Xiujuan Wu","doi":"10.1021/acsnano.4c18836","DOIUrl":null,"url":null,"abstract":"Selective four-electron mild electrochemical oxidation of benzyl alcohol to high-value-added benzoic acid is regarded as a green alternative to conventional synthesis methods under moderate conditions. Herein, we synthesize oxygen vacancy-rich amorphous/crystalline heterostructure spinel-type oxides NiCo<sub>2</sub>O<sub>4</sub> as a bifunctional electrocatalyst by a pulse voltammetry electrochemical treatment process, which can be utilized for the anode benzyl alcohol oxidation (AOR) and cathode nitrate reduction reaction (NO<sub>3</sub>RR), respectively. The designed NiCo<sub>2</sub>O<sub>4-x</sub>–25/NF delivers only 1.18 V vs RHE at 10 mA cm<sup>–2</sup>, and Faraday efficiency of benzoic acid of ∼100%. The systematic studies reveal that the amorphous structure of NiCo<sub>2</sub>O<sub>4-x</sub>–25/NF generates abundant oxygen vacancies, promoting the rapid generation of active sites and intermediate species adsorption. Meanwhile, the presence of the crystalline structure accelerates electron transfer and maintains structural stability, thereby improving overall performance. Impressively, it exhibits excellent electrocatalytic performance for AOR coupled with NO<sub>3</sub>RR in an integrated electrolyzer, achieving a current density of 100 mA cm<sup>–2</sup> at an applied low cell voltage of 1.38 V and maintaining superior catalytic stability, withstanding continuous electrolysis for 144 h. This work provides a facile synthesis approach for an amorphous/crystalline heterostructure with high electrocatalytic performance, holding great potential for paired electrosynthesis of value-added chemicals.","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"11 1","pages":""},"PeriodicalIF":16.0000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Amorphous/Crystalline Heterostructure Nickel–Cobalt Oxides with Rich Oxygen Vacancies for Electrocatalytic Production of Benzoic Acid Coupled with Nitrate Reduction\",\"authors\":\"Rushun An, Chunlai Wang, Yandong Li, Yingkai Di, Fusheng Li, Fei Li, Licheng Sun, Xiujuan Wu\",\"doi\":\"10.1021/acsnano.4c18836\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Selective four-electron mild electrochemical oxidation of benzyl alcohol to high-value-added benzoic acid is regarded as a green alternative to conventional synthesis methods under moderate conditions. Herein, we synthesize oxygen vacancy-rich amorphous/crystalline heterostructure spinel-type oxides NiCo<sub>2</sub>O<sub>4</sub> as a bifunctional electrocatalyst by a pulse voltammetry electrochemical treatment process, which can be utilized for the anode benzyl alcohol oxidation (AOR) and cathode nitrate reduction reaction (NO<sub>3</sub>RR), respectively. The designed NiCo<sub>2</sub>O<sub>4-x</sub>–25/NF delivers only 1.18 V vs RHE at 10 mA cm<sup>–2</sup>, and Faraday efficiency of benzoic acid of ∼100%. The systematic studies reveal that the amorphous structure of NiCo<sub>2</sub>O<sub>4-x</sub>–25/NF generates abundant oxygen vacancies, promoting the rapid generation of active sites and intermediate species adsorption. Meanwhile, the presence of the crystalline structure accelerates electron transfer and maintains structural stability, thereby improving overall performance. Impressively, it exhibits excellent electrocatalytic performance for AOR coupled with NO<sub>3</sub>RR in an integrated electrolyzer, achieving a current density of 100 mA cm<sup>–2</sup> at an applied low cell voltage of 1.38 V and maintaining superior catalytic stability, withstanding continuous electrolysis for 144 h. 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引用次数: 0
摘要
选择性四电子温和电化学氧化苯甲醇制备高附加值苯甲酸,是一种在中等条件下替代传统合成方法的绿色方法。本文采用脉冲伏安电化学处理工艺合成了富氧空位的非晶/晶异质结构尖晶石型氧化物NiCo2O4作为双功能电催化剂,可分别用于阳极苯甲醇氧化(AOR)和阴极硝酸还原反应(NO3RR)。设计的NiCo2O4-x-25 /NF在10 mA cm-2时仅提供1.18 V vs RHE,苯甲酸的法拉第效率为~ 100%。系统研究表明,NiCo2O4-x-25 /NF的无定形结构产生了丰富的氧空位,促进了活性位点的快速生成和中间物质的吸附。同时,晶体结构的存在加速了电子的转移,保持了结构的稳定性,从而提高了整体性能。令人印象深刻的是,它在集成电解槽中对AOR与NO3RR耦合表现出优异的电催化性能,在施加1.38 V的低电池电压下,电流密度达到100 mA cm-2,并保持了优异的催化稳定性,可以连续电解144小时。这项工作为合成具有高电催化性能的非晶/晶体异质结构提供了一种简便的方法。在成对电合成增值化学品方面具有很大的潜力。
Amorphous/Crystalline Heterostructure Nickel–Cobalt Oxides with Rich Oxygen Vacancies for Electrocatalytic Production of Benzoic Acid Coupled with Nitrate Reduction
Selective four-electron mild electrochemical oxidation of benzyl alcohol to high-value-added benzoic acid is regarded as a green alternative to conventional synthesis methods under moderate conditions. Herein, we synthesize oxygen vacancy-rich amorphous/crystalline heterostructure spinel-type oxides NiCo2O4 as a bifunctional electrocatalyst by a pulse voltammetry electrochemical treatment process, which can be utilized for the anode benzyl alcohol oxidation (AOR) and cathode nitrate reduction reaction (NO3RR), respectively. The designed NiCo2O4-x–25/NF delivers only 1.18 V vs RHE at 10 mA cm–2, and Faraday efficiency of benzoic acid of ∼100%. The systematic studies reveal that the amorphous structure of NiCo2O4-x–25/NF generates abundant oxygen vacancies, promoting the rapid generation of active sites and intermediate species adsorption. Meanwhile, the presence of the crystalline structure accelerates electron transfer and maintains structural stability, thereby improving overall performance. Impressively, it exhibits excellent electrocatalytic performance for AOR coupled with NO3RR in an integrated electrolyzer, achieving a current density of 100 mA cm–2 at an applied low cell voltage of 1.38 V and maintaining superior catalytic stability, withstanding continuous electrolysis for 144 h. This work provides a facile synthesis approach for an amorphous/crystalline heterostructure with high electrocatalytic performance, holding great potential for paired electrosynthesis of value-added chemicals.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.