{"title":"Composition-Tuned Pt-Based Nanobranch Films for Selective, Room-Temperature Gas Detection (1 ppb–100 ppm)","authors":"Maryam Barzegar, Trieu Nguyen, Juergen Jung, Gugang Chen, Shutang Chen","doi":"10.1021/acssensors.6c02042","DOIUrl":null,"url":null,"abstract":"<p>Chemiresistive gas sensors are broadly cross-sensitive, limiting quantitative use in complex mixtures. We address this challenge through materials-and-array co-design: a 480-node library of composition-tuned, dendritic Pt-based nanoparticles (Pt, Pt–Ni, Pt–Ag, Pt–Pd, Pt–Cu, and Pt–Au) was challenged with twelve medically and environmentally relevant gases at 25 °C—namely isoprene, methanol, ethanol, acetone, ammonia, formaldehyde, NO, CO, CO<sub>2</sub>, H<sub>2</sub>, CH<sub>4</sub>, and C<sub>3</sub>H<sub>8</sub>—across 1 ppb to 100 ppm. Distinct composition-dependent response fingerprints emerged: Pt–Ni produced the largest formaldehyde response observed here (approximately 2.1% at 100 ppm), whereas Pt–Pd showed the strongest preference for NO (approximately 2.9% at 50 ppm). The films formed homogeneous, percolated networks that delivered reproducible signals, with device-to-device RSD < 4.2% across 480 sensors and >90% response retention over one month at room temperature. These results establish a practical route to heater-free gas sensing through bimetallic composition and array-level response profiling, while identifying humidity validation and multivariate classification as important next steps toward practical breath and environmental applications.</p>","PeriodicalId":24,"journal":{"name":"ACS Sensors","volume":"11 10","pages":"9116–9122"},"PeriodicalIF":10.9000,"publicationDate":"2026-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Sensors","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acssensors.6c02042","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Chemiresistive gas sensors are broadly cross-sensitive, limiting quantitative use in complex mixtures. We address this challenge through materials-and-array co-design: a 480-node library of composition-tuned, dendritic Pt-based nanoparticles (Pt, Pt–Ni, Pt–Ag, Pt–Pd, Pt–Cu, and Pt–Au) was challenged with twelve medically and environmentally relevant gases at 25 °C—namely isoprene, methanol, ethanol, acetone, ammonia, formaldehyde, NO, CO, CO2, H2, CH4, and C3H8—across 1 ppb to 100 ppm. Distinct composition-dependent response fingerprints emerged: Pt–Ni produced the largest formaldehyde response observed here (approximately 2.1% at 100 ppm), whereas Pt–Pd showed the strongest preference for NO (approximately 2.9% at 50 ppm). The films formed homogeneous, percolated networks that delivered reproducible signals, with device-to-device RSD < 4.2% across 480 sensors and >90% response retention over one month at room temperature. These results establish a practical route to heater-free gas sensing through bimetallic composition and array-level response profiling, while identifying humidity validation and multivariate classification as important next steps toward practical breath and environmental applications.
期刊介绍:
ACS Sensors is a peer-reviewed research journal that focuses on the dissemination of new and original knowledge in the field of sensor science, particularly those that selectively sense chemical or biological species or processes. The journal covers a broad range of topics, including but not limited to biosensors, chemical sensors, gas sensors, intracellular sensors, single molecule sensors, cell chips, and microfluidic devices. It aims to publish articles that address conceptual advances in sensing technology applicable to various types of analytes or application papers that report on the use of existing sensing concepts in new ways or for new analytes.